Functional Aspects of Early Light-Induced Protein (ELIP) Genes from the Desiccation-Tolerant Moss Syntrichia caninervis

The early light-induced proteins (ELIPs) are postulated to act as transient pigment-binding proteins that protect the chloroplast from photodamage caused by excessive light energy. Desert mosses such as Syntrichia caninervis, that are desiccation-tolerant and homoiochlorophyllous, are often exposed to high-light conditions when both hydrated and dry ELIP transcripts are accumulated in response to dehydration. To gain further insights into ELIP gene function in the moss S. caninervis, two ELIP cDNAs cloned from S. caninervis, ScELIP1 and ScELIP2 and both sequences were used as the basis of a transcript abundance assessment in plants exposed to high-light, UV-A, UV-B, red-light, and blue-light. ScELIPs were expressed separately in an Arabidopsis ELIP mutant Atelip. Transcript abundance for ScELIPs in gametophytes respond to each of the light treatments, in similar but not in identical ways. Ectopic expression of either ScELIPs protected PSII against photoinhibition and stabilized leaf chlorophyll content and thus partially complementing the loss of AtELIP2. Ectopic expression of ScELIPs also complements the germination phenotype of the mutant and improves protection of the photosynthetic apparatus of transgenic Arabidopsis from high-light stress. Our study extends knowledge of bryophyte photoprotection and provides further insight into the molecular mechanisms related to the function of ELIPs.


Introduction
Light is an essential energy source for all plant life and is used to generate a usable carbon-based energy source for growth via photosynthesis, however, when light intensities exceed the plant's saturated photosynthesis requirements it has the potential to cause damage to the plant [1]. This potential damage is driven by an overproduction of reactive oxygen species (ROS). The oxygen concentration in chloroplasts is governed by the activity of photosystem II (PSII) and the generation of ROS from the oxygen generated by PSII, e.g., H 2 O 2 , superoxide(O 2 − ), hydroxyl radicals, and 1 O 2 * in chloroplasts is closely associated with exposure to excess light [2]. High-light intensities lead to an increase in ROS which, if not scavenged, will result in photo-oxidative damage and photoinhibition [3]. Photoinhibition in turn results in the degradation of carotenoids, bleaching of chlorophylls, and an increase in lipid peroxidation driven by the reactive-oxygen derivatives [4]. Photosynthetic organisms The cDNA sequences were used to generate transgenic Arabidopsis Atelip mutants (lacking one of the AtELIP genes (AtELIP2) constitutively expressing the ScELIPs transcripts with the aim of assessing the ability of the ScELIPs to complement the Atelip mutant phenotype under different light treatments in different growth phases.

Multiple Sequence Alignment and Phylogenetic Analysis
We identified 26 Unigenes as ScELIPs in the reference transcriptome [10], 6of which have complete open reading frames (ORFs): Unigenes 13021, 40120, 40121, 68225, 16576, and 8044. Unigene 16576 and 8044 each contain 94 predicted amino acids that were of short length to known ELIPs (Table  S1). The predicted pI of Unigene 13021 was 5.58 which was significantly lower than other ScELIPs Unigenes. Unigenes 40121 and 68225 each contain ORFs that were of comparable length to known ELIPs and encode a putative primary amino acid sequence that matched known ELIP proteins. A multiple alignment of ScELIP with other ELIPs is shown in Supplementary Figure S1, ScELIPs have two conserved ELIP domains and exhibit conserved primary sequence regions to known ELIPs [34]. Unigenes 40121 and 68225 were chosen for generation of the target ELIP transgenes and were designated ScELIP1 and ScELIP2. ScELIP1 (GeneBank number KM363766) was 995-base pair (bp) in length and contained a 711 bp ORF encoding a 236 amino acid putative polypeptide. ScELIP2 (GeneBank number KM363767) was 904 bp in length and contained a 624 bp ORF encoding a 207 amino acid putative polypeptide as shown in Table 1.  1 The early light-induced protein of Syntrichia caninervis. 2 The early light-induced protein gene 1 of Syntrichia caninervis. 3 The early light-induced protein gene 2 of Syntrichia caninervis.

Gametophytic Expression of ScELIPs in Response to Light Treatments
To elucidate whether a correlation exists between light quality and/or intensity with ScELIPs transcript abundance, the level of ScELIP1 and ScELIP2 transcripts were quantitatively assessed in total RNA from gametophytes of S.caninervis following exposure to various light regimes using RT-qPCR ( Figure 2). ScELIP1 transcript abundance rapidly declines when the gametophytes are exposed to either UVA or UVB (Figure 2a,b) and does not recover from continued exposure to UVA but exhibits an ability to recover to approximately 50% of control abundance when exposed to UVB for 2 h but not after 4 h or 12 h. ScELIP2 transcript abundance does not decline in response to exposure to either UVA or UVB but exhibits a peak increase in abundance at 4 h of exposure to UVA and after 2 h of exposure to UVB. In both treatments the level of abundance in the transcripts return to control levels at longer exposure times. In the left pannel, numbers above the lines represent bootstrap percentages (based on 1000 replicates). A bootstrap value of 100% indicates branches that were supported in all replicates of resampling of data. The scale bar indicates the number changes per unit length. The two ScELIPs were highlighted by a red star. Different colors represent different evolving groups, pink (bryophytes), blue (ferns), purple (monocots), and green (eudicots). In the right pannel, the conserved domain of ELIPs corresponding to the left pannel.

Gametophytic Expression of ScELIPs in Response to Light Treatments
To elucidate whether a correlation exists between light quality and/or intensity with ScELIPs transcript abundance, the level of ScELIP1 and ScELIP2 transcripts were quantitatively assessed in total RNA from gametophytes of S.caninervis following exposure to various light regimes using RT-qPCR ( Figure 2). ScELIP1 transcript abundance rapidly declines when the gametophytes are exposed to either UVA or UVB (Figure 2a,b) and does not recover from continued exposure to UVA but exhibits an ability to recover to approximately 50% of control abundance when exposed to UVB for 2 h but not after 4 h or 12 h. ScELIP2 transcript abundance does not decline in response to exposure to either UVA or UVB but exhibits a peak increase in abundance at 4 h of exposure to UVA and after 2 h of exposure to UVB. In both treatments the level of abundance in the transcripts return to control levels at longer exposure times.
ScELIP1 transcript abundance increased 7-fold after 4 h of exposure to red-light ( Figure 2c) and to similar levels in response to blue-light exposure after 4 h (Figure 2d). ScELIP2 transcript abundance only increased slightly in response to red-light and only after 4 h of exposure (Figure 2c), but the transcript abundance steadily increased in response to prolonged exposure to blue-light ( Figure 2d). In the left pannel, numbers above the lines represent bootstrap percentages (based on 1000 replicates). A bootstrap value of 100% indicates branches that were supported in all replicates of resampling of data. The scale bar indicates the number changes per unit length. The two ScELIPs were highlighted by a red star. Different colors represent different evolving groups, pink (bryophytes), blue (ferns), purple (monocots), and green (eudicots). In the right pannel, the conserved domain of ELIPs corresponding to the left pannel.
ScELIP1 transcript abundance increased 7-fold after 4 h of exposure to red-light ( Figure 2c) and to similar levels in response to blue-light exposure after 4 h (Figure 2d). ScELIP2 transcript abundance only increased slightly in response to red-light and only after 4 h of exposure ( Figure 2c), but the transcript abundance steadily increased in response to prolonged exposure to blue-light ( Figure 2d).
ScELIP1 transcript abundance increased approximately 5-fold after exposure to red-light for 2 h followed by blue-light for 2 h indicating that blue-light only dampened the response of ScELIP1 to red-light ( Figure 2c). When the treatment was reversed, ScELIP1 transcript abundance was unaltered from control levels indicating that red-light prevented the transcript abundance response to blue-light ( Figure 2d). ScELIP2 transcript abundance, in response to the identical dual light treatments, was elevated 15-fold with a 2 h exposure to red-light followed by 2 h of blue-light, but exhibited no response when 2 h of blue-light was followed by 2 h of red-light. Thus indicating, as for ScELIP1 transcript abundance, red-light inhibited the blue-light response.
The transcript abundance for both ScELIPs increase with increasing white light intensity. ScELIP1 transcript abundance increases linearly with increasing light intensity above 60 µmol/m 2 /s to a maximum abundance 9-fold higher than the dark control at 1500 µmol/m 2 /s (Figure 2e). ScELIP2 transcript abundance increases to a maximum level at 8-fold higher than the dark control at 750 µmol/m 2 /s but declined significantly when light intensity reached 1500 µmol/m 2 /s ( Figure 2e). was elevated 15-fold with a 2 h exposure to red-light followed by 2 h of blue-light, but exhibited no response when 2 h of blue-light was followed by 2 h of red-light. Thus indicating, as for ScELIP1 transcript abundance, red-light inhibited the blue-light response.
The transcript abundance for both ScELIPs increase with increasing white light intensity. ScELIP1 transcript abundance increases linearly with increasing light intensity above 60 μmol/m 2 /s to a maximum abundance 9-fold higher than the dark control at 1500 μmol/m 2 /s (Figure 2e). ScELIP2 transcript abundance increases to a maximum level at 8-fold higher than the dark control at 750 μmol/m 2 /s but declined significantly when light intensity reached 1500 μmol/m 2 /s ( Figure 2e).

Figure 2.
ScELIP1 and ScELIP2 transcript relative abundance assessments in Syntrichia caninervis gametophores exposed to various light treatments. The mean (each column) and SD (error bar) were calculated with three biological replicates and three technical replicates of each biological replicates. * p < 0.05; ** p < 0.01. P-values were obtained from Dunnett's T3 test comparing different time points and treatment with control. Asterisk represents statistically significant difference with 0 h in (a-d), and 0 μmoL/m 2 /s in (e). ultra violet A (UVA) light treatment (a), ultra violet B (UVB) light treatment (b), red-light treatment (c), blue-light treatment (d), high-light treatment (e).

Figure 2.
ScELIP1 and ScELIP2 transcript relative abundance assessments in Syntrichia caninervis gametophores exposed to various light treatments. The mean (each column) and SD (error bar) were calculated with three biological replicates and three technical replicates of each biological replicates. * p < 0.05; ** p < 0.01. P-values were obtained from Dunnett's T3 test comparing different time points and treatment with control. Asterisk represents statistically significant difference with 0 h in (a-d), and 0 µmoL/m 2 /s in (e). ultra violet A (UVA) light treatment (a), ultra violet B (UVB) light treatment (b), red-light treatment (c), blue-light treatment (d), high-light treatment (e).

Transgenic Lines
We obtained 15 ScELIP1 and 22 ScELIP2 transgenic T1 lines following the initial hygromycin screen of T0 transformants ( Figures S4 and S5). RT-PCR and quantitative real time PCR validated transcript abundance of transgenic lines of ScELIPs ( Figures S6 and S7), the transcript abundance of 35S-ScELIP1 and 35S-ScELIP2 transgenic lines were 5-fold to 23-fold higher than the Atelip mutant. In normal condition, there isn't't visible phenotype difference between the Col-0 WT, the Atelip mutant, and the ScELIPs transgenic lines. Finally, we chose three transgenic lines of each gene construct that had significant expression levels, and named as ScELIP1-line 1, line 2, line 3, and ScELIP2-line 1, line 2, line 3.

Germination and Early Seedling Growth under Different Light Treatments
To assess the effect of the expression of ScELIP constructs on seed germination under different light stress conditions, germination performance and early seedling morphology was assessed over a seven-day period for mature seeds of the Col-0 WT, the Atelip mutant, and two of each of the 35S-ScELIP1 and 35S-ScELIP2 transgenic Atelip lines ( Figure S8 and Figure 3). The Col-0 WT, Atelip mutant, and the two transgenic had no significant difference. The Col-0 WT and the two transgenic lines had significantly higher germination rates than the Atelip mutant until day 4 when red-light (Figure 3c,d) or blue-lightblue-light (Figure 3e,f) was used as the single light source. Germination under UVB light, the Col-0 WT had a significantly higher germination rate than either the Atelip mutant or the 35S-ScELIP transgenic lines, which had almost identical germination rates, up to 4 days after imbibition (Figure 3g,h). High-light irradiation (1500 µmol/m 2 /s) resulted in a one-day delay of germination for all genotypes (Figure 3i,j). Under high-light, the germination rate for the Col-0 WT was faster than either the Atelip mutant or the 35S-ScELIP transgenic lines up to day 5, the germination rates for the 35S-ScELIP transgenic lines, however, were significantly faster than the Atelip mutant up to day 4 ( Figure 3i,j). Expression of ScELIPs in the Atelip mutant increase germination rates but the rates do not attain WT rates when grown in red, blue, UVB, and high-light conditions.   Exposure to light from each of the sole light sources altered the initial seedling morphology in all genotypes: Red-light severely reduced the size of seedlings and caused hypocotyls elongation, blue-lightblue-light enlarged cotyledons and extended hypocotyls, UVB light resulted in failure of the cotyledons to open and a shortened hypocotyl, and high-light resulted in reduced hypocotyl extension as shown in Figure S8.

Light Treatment Effects on 7-Day Old Seedling Growth and Morphology
Seven-day old seedlings of the Col-0 WT, Atelip mutant, and 35S-ScELIP1 and 35S-ScELIP2 transgenic lines were exposed to 4 different light treatments; control conditions, red-light only, blue-light only, and UVB light for seven days and the resulting phenotypes were recorded ( Figure S9) and growth parameters quantified ( Figure 4). Under normal conditions, the Col-0 WT, Atelip, and transgenic lines showed no difference in seedling morphology ( Figure S9a Figure 4d). Under blue-light alone, the overall root length was significantly reduced for all genotypes compared to the control ( Figure 4a). Conversely, the seven-day exposure to blue-light resulted in an approximate ten-fold increase in secondary root and the increase was significantly greater for the Atelip mutant and the 35S-ScELIP transgenics ( Figure S9c,g and Figure 4b). Exposure to blue-light also resulted in chlorosis of the leaves of the Col-0 WT with a concurrent reduction in chlorophyll, however, the Atelip mutant and the 35S-ScELIP transgenics remained green and the chlorophyll content was only reduced to approximately 50% of the controls (Figure 4d). The UVB treatments inhibited seedlings growth in all genotypes with large reductions in root length and leaf number ( Figure S9d,h and Figure 4a,c). The leaf chlorophyll contents also declined when compared to controls but the seedlings remained green for all genotypes (Figure 4d).

Light Treatment Effects on 7-Day Old Seedling Growth and Morphology
Seven-day old seedlings of the Col-0 WT, Atelip mutant, and 35S-ScELIP1 and 35S-ScELIP2 transgenic lines were exposed to 4 different light treatments; control conditions, red-light only, bluelight only, and UVB light for seven days and the resulting phenotypes were recorded ( Figure S9) and growth parameters quantified ( Figure 4). Under normal conditions, the Col-0 WT, Atelip, and transgenic lines showed no difference in seedling morphology ( Figure S9a   , Total chlorophyll content in milligram (mg) per gram fresh weight. Error bars represent the SD of three biological repeats. ** p < 0.01, P-values were obtained from Dunnett's T3 test comparing the 35-SScELIP lines with Atelip mutant. P-values also were obtained from Dunnett's T3 test comparing the control (normal light condition), red, blue, and UVB light with each other. Asterisk represents statistically significant difference within one group or among specific groups delineated by the brackets.

Seedling Growth of WT and Transgenic Lines under High-Light Conditions
Seven-day old seedlings of the Col-0 WT, Atelip mutant, and transgenic lines were exposed to high-light stress (1500 µmol/m 2 /s), and morphology and the chlorophyll contents were monitored after 2 h exposure and 24 h recovery 22 ± 2 • C with a 14 h light/10 h dark cycle, and 60-75% relative humidity, and light at PPFD of 100 µmol/m 2 /s ( Figure 5). Following the high-light exposure, the transgenic lines appeared greener than the Col-0 WT and Atelip (Figure 5a,b) which was reflected in the chlorophyll contents that were significantly increased ( Figure 5c). Corresponding with chlorophyll contents, carotenoid contents of the transgenic lines were significantly higher than the Col-0 WT and Atelip mutant (Figure 5d).

Seedling Growth of WT and Transgenic Lines under High-Light Conditions
Seven-day old seedlings of the Col-0 WT, Atelip mutant, and transgenic lines were exposed to high-light stress (1500 μmol/m 2 /s ), and morphology and the chlorophyll contents were monitored after 2 h exposure and 24 h recovery 22 ± 2 °C with a 14 h light/10 h dark cycle, and 60%-75% relative humidity, and light at PPFD of 100 μmol/m 2 /s ( Figure 5). Following the high-light exposure, the transgenic lines appeared greener than the Col-0 WT and Atelip (Figure 5a,b) which was reflected in the chlorophyll contents that were significantly increased (Figure 5c). Corresponding with chlorophyll contents, carotenoid contents of the transgenic lines were significantly higher than the Col-0 WT and Atelip mutant (Figure 5d).

The Effect of High-Light Stress on Arabidopsis Plantlets
Four-week old Arabidopsis plantlets, including WT, Atelip mutant, and two transgenic lines of ScELIP1 and ScELIP2, were exposed to high-light stress (1000 μmol/m 2 /s) for 3 days and continuously for 3 weeks. The effect of high light appears to be more severe in the Atelip mutant line after the 3day treatment than the Col-0 WT and all of the 35S-ScELIP transgenic lines ( Figure 6). All genotypes were severely affected by 3 weeks of exposure to high-light, although the Atelip mutant does appear to be more severely damaged.
The chlorophyll fluorescence parameters measured were consistent with visual estimates of leaf damage. The 3-day high-light treatment resulted in a significant decline in the Fv/Fm values ( Figure  7) indicative of an inhibition photosynthesis under high-light stress. After 3 days of high-light treatment, the Fv/Fm values were so low as to be unreliable and/or undetectable so this data was not added to the analysis. The chlorophyll fluorescent parameters decreased as the stress time extend in all Arabidopsis, it indicated that high-light increased the decline of parameters, the PSII complex have been photo-inactivated, and chlorophyll began to degrade (Figures 6 and S10), a severely compromised photosynthetic apparatus. However, the 35S-ScELIPs lines exhibit a higher retention of the Fv/Fm (Figure 7), indicating an increase in protection from photo-induced inactivation and thus potentially overcoming the lack of the ELIP2 gene product that is missing in the Atelip mutant.

The Effect of High-Light Stress on Arabidopsis Plantlets
Four-week old Arabidopsis plantlets, including WT, Atelip mutant, and two transgenic lines of ScELIP1 and ScELIP2, were exposed to high-light stress (1000 µmol/m 2 /s) for 3 days and continuously for 3 weeks. The effect of high light appears to be more severe in the Atelip mutant line after the 3-day treatment than the Col-0 WT and all of the 35S-ScELIP transgenic lines ( Figure 6). All genotypes were severely affected by 3 weeks of exposure to high-light, although the Atelip mutant does appear to be more severely damaged.
The chlorophyll fluorescence parameters measured were consistent with visual estimates of leaf damage. The 3-day high-light treatment resulted in a significant decline in the F v /F m values (Figure 7) indicative of an inhibition photosynthesis under high-light stress. After 3 days of high-light treatment, the F v /F m values were so low as to be unreliable and/or undetectable so this data was not added to the analysis. The chlorophyll fluorescent parameters decreased as the stress time extend in all Arabidopsis, it indicated that high-light increased the decline of parameters, the PSII complex have been photo-inactivated, and chlorophyll began to degrade ( Figure 6 and Figure S10), a severely compromised photosynthetic apparatus. However, the 35S-ScELIPs lines exhibit a higher retention of the F v /F m (Figure 7), indicating an increase in protection from photo-induced inactivation and thus potentially overcoming the lack of the ELIP2 gene product that is missing in the Atelip mutant.  Pigment contents were measured prior to the treatment (time zero), after 3 days and after 3 weeks of the high-light treatment. Both chlorophyll a and b and carotenoid contents decreased in both the 3-day and 3-week treatments with high-light ( Figure S10a-d). Although, the pigment content of the 35S-ScELIPs lines were not elevated with respect to the Col-0 WT controls they were significantly greater than the levels measured in the Atelip mutant line, indicating that the 35S-ScELIPs constructs can rescue the Atelip mutant with regards to the effect of a lack of ELIP2 on highlight induced photodamage and pigment loss. The apparent rescue of the effect of the Atelip mutation on photosynthetic capacity is also reflected in the overall restoration of the Chla/Chlb and Car/Chl ratio of all 35S-ScELIPs ( Figure S10d-e).
Transcript abundance was assessed for ScELIP1 and ScELIP2 and other photosynthesis related genes, in all genotypes, before treatment (0 h), after 2 h, 3 days, and 3 weeks exposure to high-light stress using RT-qPCR (Figure 8). ScELIP1 and ScELIP2 exhibit moderate levels in the controls (0 h), presumably indicating the level of expression obtained with the 35S promoter. ScELIP1 transcript abundance rapidly increased 35-70-fold in the 35S-ScELIP1 lines following exposure to high-light for 2 h but subsequently declines to low abundance after 3 days and negligible levels after 3 weeks of exposure to high-light (Figure 8a). ScELIP2 transcripts rapidly declined in abundance upon exposure of the 35S-ScELIP2 transgenic to high-light, however, ScELIP2 transcript abundance significantly increased to 49-69-fold in response to prolonged exposure to high-light for 3 weeks (Figure 8b).  Pigment contents were measured prior to the treatment (time zero), after 3 days and after 3 weeks of the high-light treatment. Both chlorophyll a and b and carotenoid contents decreased in both the 3-day and 3-week treatments with high-light ( Figure S10a-d). Although, the pigment content of the 35S-ScELIPs lines were not elevated with respect to the Col-0 WT controls they were significantly greater than the levels measured in the Atelip mutant line, indicating that the 35S-ScELIPs constructs can rescue the Atelip mutant with regards to the effect of a lack of ELIP2 on highlight induced photodamage and pigment loss. The apparent rescue of the effect of the Atelip mutation on photosynthetic capacity is also reflected in the overall restoration of the Chla/Chlb and Car/Chl ratio of all 35S-ScELIPs ( Figure S10d-e).
Transcript abundance was assessed for ScELIP1 and ScELIP2 and other photosynthesis related genes, in all genotypes, before treatment (0 h), after 2 h, 3 days, and 3 weeks exposure to high-light stress using RT-qPCR (Figure 8). ScELIP1 and ScELIP2 exhibit moderate levels in the controls (0 h), presumably indicating the level of expression obtained with the 35S promoter. ScELIP1 transcript abundance rapidly increased 35-70-fold in the 35S-ScELIP1 lines following exposure to high-light for 2 h but subsequently declines to low abundance after 3 days and negligible levels after 3 weeks of exposure to high-light (Figure 8a). ScELIP2 transcripts rapidly declined in abundance upon exposure of the 35S-ScELIP2 transgenic to high-light, however, ScELIP2 transcript abundance significantly increased to 49-69-fold in response to prolonged exposure to high-light for 3 weeks (Figure 8b). Pigment contents were measured prior to the treatment (time zero), after 3 days and after 3 weeks of the high-light treatment. Both chlorophyll a and b and carotenoid contents decreased in both the 3-day and 3-week treatments with high-light ( Figure S10a-d). Although, the pigment content of the 35S-ScELIPs lines were not elevated with respect to the Col-0 WT controls they were significantly greater than the levels measured in the Atelip mutant line, indicating that the 35S-ScELIPs constructs can rescue the Atelip mutant with regards to the effect of a lack of ELIP2 on high-light induced photodamage and pigment loss. The apparent rescue of the effect of the Atelip mutation on photosynthetic capacity is also reflected in the overall restoration of the Chla/Chlb and Car/Chl ratio of all 35S-ScELIPs ( Figure S10d-e).
Transcript abundance was assessed for ScELIP1 and ScELIP2 and other photosynthesis related genes, in all genotypes, before treatment (0 h), after 2 h, 3 days, and 3 weeks exposure to high-light stress using RT-qPCR (Figure 8). ScELIP1 and ScELIP2 exhibit moderate levels in the controls (0 h), presumably indicating the level of expression obtained with the 35S promoter. ScELIP1 transcript abundance rapidly increased 35-70-fold in the 35S-ScELIP1 lines following exposure to high-light for 2 h but subsequently declines to low abundance after 3 days and negligible levels after 3 weeks of exposure to high-light (Figure 8a). ScELIP2 transcripts rapidly declined in abundance upon exposure of the 35S-ScELIP2 transgenic to high-light, however, ScELIP2 transcript abundance significantly increased to 49-69-fold in response to prolonged exposure to high-light for 3 weeks (Figure 8b). ScELIP2 transcripts did not accumulate to significant levels in the Col-0 WT even after exposure to high-light for 3 weeks.
dramatically elevated in abundance in the samples exposed for 3 weeks (Figure 8h).
In the Col-0 WT, PSBD transcript abundance was elevated 5-fold after 3 days of exposure and remained elevated throughout the high-light treatment but in the 35S-ScELIP transgenic lines PSBD transcripts only accumulated to elevated levels in the 3-week exposure samples. The PSBD transcript abundance in the Atelip mutant remained at relatively low levels throughout the treatment ( Figure  8i). PSBS transcript abundance initially high in the control leaves of the 35S-ScELIP1 lines declined in response to exposure to high-light with a moderate recovery at 3 weeks. PSBS transcript abundance in the control Col-0 WT exhibited a similar response to that of the 35S-ScELIP1 lines but made a full recovery at 3 weeks. In the 35S-ScELIP2 lines, PSBS transcript abundance maintained initial levels through the first 3 days of exposure to highlight but were significantly elevated above control levels at 3 weeks (Figure 8c).  Transcript abundance for 3 of the AtELIP family of related proteins were also altered in response to high-light. The abundance of OHP transcripts peaked at 3 days of exposure to high-light in Col-0 WT and also in the 35S-ScELIPs lines but to a lesser extent. The OHP transcripts in the 35S-ScELIPs lines were significantly more abundant than the same transcript in the Atelip mutant. In all cases OHP transcripts declined in abundance at 3 weeks (Figure 8d). OHP2 transcripts accumulate to levels 5-15-fold greater than control levels (0 h) in the Col-0 WT and 35S-ScELIPs lines after 3 weeks of exposure to high-light and to levels significantly greater than in the Atelip mutant (Figure 8e). SEP2 transcripts increased in abundance after exposure to high-light for 2 h in the Col-0 WT and 35S-ScELIPs lines, in both cases to higher levels than in the Atelip mutant, declined after 3 days of high-light exposure and then returned to near control levels after 3 weeks (Figure 8f).
LHCA2 transcripts declined in abundance response to exposure to high-light at 2 h and 3 days, and slightly increased at 3 weeks in the 35S-ScELIP lines. However, in the Col-0 WT LHCA2 transcripts increased in abundance after 3 days of high-light exposure and remained high throughout the length of the treatment (Figure 8g). LHCB4.2 transcript abundance in the Atelip mutant, remained constant throughout the 3-week exposure to high-light. In the Col-0 WT and both transgenic lines, LHCB4.2 transcript abundance declined during the first 3 days of exposure to high-light but was dramatically elevated in abundance in the samples exposed for 3 weeks (Figure 8h).
In the Col-0 WT, PSBD transcript abundance was elevated 5-fold after 3 days of exposure and remained elevated throughout the high-light treatment but in the 35S-ScELIP transgenic lines PSBD transcripts only accumulated to elevated levels in the 3-week exposure samples. The PSBD transcript abundance in the Atelip mutant remained at relatively low levels throughout the treatment (Figure 8i). PSBS transcript abundance initially high in the control leaves of the 35S-ScELIP1 lines declined in response to exposure to high-light with a moderate recovery at 3 weeks. PSBS transcript abundance in the control Col-0 WT exhibited a similar response to that of the 35S-ScELIP1 lines but made a full recovery at 3 weeks. In the 35S-ScELIP2 lines, PSBS transcript abundance maintained initial levels through the first 3 days of exposure to highlight but were significantly elevated above control levels at 3 weeks (Figure 8c).

Discussion
In this study, we identified and characterized two ELIP genes from the S. caninervis transcriptome. ScELIP1 has close primary amino acid sequence similarity to the ELIPs of the non-vascular plants Physcomitrella patens, Sphagnum fallax, and Syntrichia ruralis [21] excepting one kind of fern (Onoclea sensibilis). ScELIP2 that is more similar to the ELIPs of vascular plants such as Arabidopsis [26], Zea mays [35], etc. (Figure 1). According to the amino acid sequence similarity of ELIPs, bryophytes ELIPs were clearly separated from monocots and eudicots ELIPs, because bryophytes are a special evolutionary group. Neither of the ScELIP sequences fully corresponds to either of the two Arabidopsis ELIP genes which, by ectopically expressing the ScELIP genes independently in the Arabidopsis Atelip mutant background, allowed us to evaluate both the possible activity of the ScELIP transcripts in photoprotection of chloroplasts in situ but also to determine if the moss ELIPs could rescue the Atelip phenotype resulting from the loss of AtELIP2.
In Syntrichia caninervis ScELIP1 and ScELIP2 transcripts abundance were elevated by different light stresses (Figure 2). ScELIP1 and ScELIP2 transcripts exhibit similar responses, both exhibit greater accumulation in response to blue and high-light exposure and both exhibit transcript accumulation only after a 4 h exposure to red-light, more evident for ScELIP1. Our understanding of how or why ELIPs respond to different light qualities is still very limited, but in pea seedlings ELIPs transcripts are specifically induced by blue-light but not by red-light, and the accumulation of blue-light induced ScELIPs transcripts are significantly repressed by low intensity red-light [23]. These findings are consistent with the S. caninervis data presented here with the exception that prolonged exposure to red-light alone does result in an elevation ScELIP transcript abundance. The two Arabidopsis ELIP genes can be induced in dark grown Arabidopsis exposed to illumination by high intensities of both red and blue-light [18] which again are consistent with observations. In Arabidopsis, ELIP transcript abundance was elevated by UVA but not by UVB [36]. In S. caninervis, ScELIP1 transcripts declined in abundance in response to UVA and ScELIP2 transcript levels only exhibited a response to UVA after a 4 h exposure (Figure 2a). UVB exposure caused a general decline in ScELIP1 transcripts but generated an increase in abundance of ScELIP2 transcripts after 2 h of exposure. Clearly, the S. caninervis ELIP response to UV light differs from that seen in Arabidopsis, perhaps indicating a more complex role in UV protection mechanisms in the moss. However, this possibility must be tempered by differences in experimental protocols and by the distinct possibility that the moss genome contains more than two ELIP genes as would be suggested by the observation that the genomes of desiccation tolerant plants are rich in ELIP genes [33].
It is clear from our analyses that ELIP transcript abundance in S. caninervis is altered by light quality (UVA and B, red and blue-light), suggesting that the promoters that control the transcription of ELIP genes contain elements that respond to light signal transduction pathways. At the present time, the promoter sequences for the S. caninervis ELIP genes are unavailable but ELIP promoters from other species have been investigated. In Ginkgo biloba, high-light defense and stress responsive elements were delineated in the promoter region of GbELIP [37]. In Arabidopsis, ELIP1 expression is enhanced by red, far-red, and blue-light and that phytochrome A and B are involved in the signaling pathway along with the transcription factor HY5 [18]. The Arabidopsis ELIP2 promoter region was later demonstrated to contain two regulatory elements, that form a regulatory unit, that regulate ELIP2 expression in response to UVB, high-light, and cold stress [38]. If similar elements appear, the ScELIP promoter might add to our understanding of the evolution of light response transduction pathways in plants.
The significant and rapid elevation in the ScELIPs transcript abundances when gametophytes are transferred from the dark to high-light is consistent with similar observations in Arabidopsis [39], Hordeum vulgare [25], Pisum sativum [23], D. salina [20], and Syntrichia ruralis [21] and supportive of the hypothesis that ELIPs are useful indicators of high-light stress and the initiation of photoprotection mechanisms during the early phases of photodamage [40].
Light stress has been demonstrated to exert influence on seed germination and photomorphogenesis during the initial developmental stages of seedling growth [17]. Our results supported the observation that light quality alters photomorphogenesis following germination (Supplementary Figure S8) such that the hypocotyl was shortened and the cytoledons remained closed following germination under UVB light [41]. In a recent report, UVB photoreceptor UVR8 (UV resistance locus 8) promotes rapid PIF (phytochrome interacting factors) degradation and reduces PIF abundance, which lead to UVB inhibits shade avoidance, finally, UVB inhibits stem elongation of Sharma et al. [42]. While this phenotype was not altered by the expression of the 35S-ScELIPs in the transgenic seeds. The addition of the 35S-ScELIPs genes into the Atelip mutant line significantly improved the germination rate above that of the mutant alone without altering leaf number, root number, or root length with the exception of an increase in root number in the 35S-ScELIP transgenics under blue-light ( Figure 4).
The complementation of the 35S-ScELIP genes to the Atelip mutant line enhanced the survival rate of seedlings under high-light stress in part by minimizing chlorophyll degradation. The transgenic lines, by protecting the chlorophyll, were greener in appearance than even the Col-0 WT lines after 24 h of recovery following exposure to high-light conditions and also had a higher percent survival ( Figure 5). This was also evident in the more mature plant, where the transgenic lines exhibited significantly less photodamage under prolonged exposure to high-light intensities than the mutant line ( Figure 6). The improved protection to photodamage observed in the 35S-ScELIP transgenics was reflected in their improved photosynthetic performance measures compared to the Atelip mutant increased F v /F m (Figure 7). These data suggest that the ScELIPs can protect PSII functionality of Arabidopsis plantlets under high-light conditions. ELIP accumulation under high-light stress has been correlated with photoinhibition of PS, degradation of the D1 protein, and changes in the level of pigments in the mature plant [36,43]. These conclusions are consistent with our data indicating enhanced PSII protection in the 35S-ScELIP transgenics.
The results of this study indicate that the physiological function of ELIPs are related to the protection of chlorophyll, and thus enhance the protection of the chloroplasts from photooxidative stress. The 35S-ScELIP1 and 35S-ScELIP2 lines also have improved carotenoid levels than those recorded for the Atelip mutant following high-light exposure and thus it is possible that ScELIPs may also play a role in stabilizing the photosynthetic apparatus and is consistent with the idea that ELIP acts as a photoprotectant for PSII in the thylakoid membrane and as such would play a major role in the ability of Syntrichia caninervis to survive in extreme conditions, as suggested by VanBuren et al. [33], and that it regularly encounters in the Gobi Desert.
The 35S-ScELIP1 and 35S-ScELIP2 lines have a significant response to high-light (Figure 8a,b) even though their transcription is controlled by the 35S promoter. It is possible that the overall transcription rates affected by high-light or transcript abundance under high-light is partially controlled by transcript stability. The former seems unlikely given the variability in transcript abundance for other genes in response to high-light (Figure 8). It is possible that transcript abundance was controlled in part by the altered stability but this possibility was not investigated. It is also possible that the 35S promoter used in these constructs is affected by exposure to high-light but there are no reports of this as a possible explanation. It is intriguing that the transcript abundance profile for ScELIP1 is more similar to the native Arabidopsis SEP2 and the transcript abundance profile for ScELIP2 is more similar to OHP2 than to other photosynthetic related transcripts. If the 35S promoter, which is active in the untreated controls, is not high-light inducible then it could suggest the presence of a post-transcriptional mechanism that may control the abundance of the transcripts of three ELIP families of protective proteins. The transcript abundance profiles in response to both short and long exposure to high-light for all of the photosynthetic related transcripts in the genotypes we investigated were complex. However, it was evident that the Atelip mutant was, with the exception of the SEP2 transcript which was elevated above control levels (Figure 8f), deficient in proteins that function to protect PSII. The ectopic expression of the ScELIP transcripts in the Atelip mutant appears to provide the necessary protective proteins (at least the transcripts) which overcomes the high-light phenotype of the mutant. In addition, the transcript abundance profiles for all genes and genotypes indicate either a recovery of or elevation in transcript abundance after 3 weeks of exposure to high-light which may be indicative of the ability of Arabidopsis to acclimate to this environmental stress.

Plant Material and Growth Conditions
Dry Syntrichia caninervis gametophytes were collected from the Gurbantunggut Desert in the Xinjiang Uygur Autonomous Region, China (44 • 32 30" N, 88 • 6 42" E) and kept in the dark in a paper sack at room temperature. Dry gametophytes were fully hydrated on filter paper saturated with MINIQ-filtered water (8 mL) in glass petri dishes for 24 h at 25 • C, with light at a photosynthetic photon flux density (PPFD) of 50 µmol/m 2 /s, prior to the described light treatments.
Seeds of Arabidopsis thaliana L. cv. Columbia and the Arabidopsis mutant Atelip were germinated on MS medium [44] after surface sterilization with 70% ethanol for 30 s followed by 3% sodium hypochlorite for 7 min and washed 5 times with sterile water. Seedlings were transferred to 5 cm diameter pots at 4-6 leaf stage containing autoclaved peat substrate (Pindstrup, Mosebrug) and grown under controlled conditions at 22 ± 2 • C with a 14 h light/10 h dark cycle, 60-75% relative humidity, and light at PPFD of 100 µmol/m 2 /s. A. thaliana (Col-0) and the mutant Atelip (NASC ID: N544166), a T-DNA insertion mutant in the promoter region of ELIP2 [45], were obtained from The European Arabidopsis Stock Centre.

Bioinformatic Analysis of Syntrichia Caninervis ELIP Sequences
Publicly available ELIP sequences of A. thaliana and Physcomitrella patens were used to screen the transcriptome of S. caninervis [10] for single copy transcripts (designated as unigenes) that were putative ELIP coding sequences. We translated each unigene to obtain the amino acid sequence using ORF finder. All generated amino acid sequences were investigated using NCBI-blastp. The final sequences used to construct the ScELIP clones were consistent with annotated ELIP genes in the NCBI database. A molecular phylogeny was constructed using MEGA7.0 with the neighbor-joining method and 500 bootstrap replicates [46] utilizing the eudicots, monocots, ferns, and bryophytes ELIP sequences obtained from public resources and presented in additional data ( Table S2). All of ELIP genes domain prediction was conducted with the Pfam database (http://pfam.xfam.org/search). Further physiological and biochemical properties prediction for two ScELIPs was obtained on ExPASy (https://www.expasy.org/).

Extraction of RNA and RT-qPCR Based Expression Analysis
Total RNA was isolated from 0.1 g of S. caninervis gametophytes using the TRIzol reagent (Qiagen, Berlin, Germany) according to the manufacturer's protocol. The cDNA was synthesized from 1 µg of total RNA using random hexamer primers with the PrimeScript RT reagent kit including gDNA Eraser (Real time; Takara, Japan) according to the manufacturer's protocol and stored at -20 • C until use. The cDNA was diluted 10-fold with H 2 O to serve as a template for Real-time PCR. Each 20 µL real-time PCR reaction contained 2 µL cDNA, 0.5 µL each of forward and reverse primers as indicated below (10 µM for each primer), and 10 µL of SYBR Premix Ex Taq TM (Takara Biomedical Technology, Takara, Japan). Real-time quantitative PCR was performed in 96-well plates with the CFX96 Real-Time PCR Detection System (Bio-Rad, New York, NY, USA) according to the manufacturer's instructions [47], with three technical replicates and two biological replicates. The RT-qPCR protocol was as follows: 30 s initial denaturation at 95 • C, 40 cycles of 94 • C for 5 s, and 60 • C for 30 s. Parallel reactions to amplify α-TUB2 were used to normalize the amount of template. The forward and reverse primers used for ScELIP1 were 5 GGCTATGCTGGGATTCGTGT 3 and 5 TTGATCTGGTTCCTGGCGTC 3 , the primers for ScELIP2 were 5 GCAATGATCGGACTTGTCGC3 and 5 ACCTGCTGTGAACAATCCGT 3 . All PCR efficiencies were >95%. Transcript abundance data were collected using Bio-Rad CFX Manager.
Hydrated S. caninervis gametophytes were exposed to the following environmental treatments: A progressive series of PPFD, Ultraviolet A (UVA), Ultraviolet B (UVB), red-light, and blue-light. Fully hydrated S. caninervis gametophytes were transferred to MINIQ-filtered water saturated filter paper in clean petri dishes for all treatments. The light series treatment consisted of a 2 h exposure to either 0 µmol/m 2 /s, 60 µmol/m 2 /s, 225 µmol/m 2 /s, 750µmol/m 2 /s, or 1500 µmol/m 2 /s provided by a cool-white fluorescent light lamp (Philips lighting). For the ultraviolet radiation treatment gametophytes were exposed to either UVA (380 nm) or UVB (308 nm) irradiation for 0 h, 1 h, 2 h, 4 h, 12 h under a fluorescent light lamp (Philips lighting) that delivered a PPFD of 10 µmol/m 2 /s. In the red-light treatment, gametophytes were either exposed to red-light using a monochromatic light-emitting diode (LED, Philips lighting, Amsterdam, Netherlands) at 655 nm, and PPFD of 100 µmol/m 2 /s for 0, 2, 4 h, or exposed to red-light for 2 h and then transferred to blue-light for 2 h. In the blue-light treatment gametophytes were either exposed to blue-light using a monochromatic light-emitting diode (LED, Philips lighting) at 450 nm and PPFD of 100 µmol/m 2 /s for 0 h, 2 h, 4 h, or exposed to blue-light for 2 h and then transferred to red-light for 2 h. Each treatment consisted of three biological replicates.

Cloning of ScELIP Genes and Establishment of Transgenic Lines
The transcripts ScELIP1 (Unigene 40121) and ScELIP2 (Unigene 68225) were chosen from the Syntrichia caninervis transcriptome database [10]. The full-length coding sequence for each gene product was obtained by RT-PCR using the cDNA previously constructed for the RT-qPCR based expression analysis. The RT-PCR was performed using gene-specific primers: For ScELIP1 the forward and reverse primers were 5 GGGGTACCC ATGGCAGCGATGGCG 3 and 5 CGAGATCTCGCTAGACAGGGAAGCG 3 , and these primers include inserted KpnI and XbalI enzyme sequences. For ScELIP2, the forward and reverse primers were 5 CGGGATCCATGGCGATGACTTT 3 and 5 CGAGATCTCGTTATACAAGTGGGC 3 , and these primers include Bam HI and XbalI site sequences. The PCR product was extracted from agarose gel electrophoresis (0.8% agarose, 5 v/cm voltage for 20 min) using the Gel Extraction Kit (OMEGA, St. Louis, MI, USA), and 4 µL PCR extract production, 1 µL pMD 19-T vector, 1 µL T4 DNA ligase, 2 µL 10× ligation buffer, and 12 µL H 2 O for 2 h (TaKaRa, Japan), linking the product with pMD 19-T vector. The sequences were validated by sanger sequencing at the Beijing Genomics Institute (BGI) to ensure that there were no PCR introduced mutations into the coding sequences.

Transformation of A. Thaliana
The ScELIP1 ORF was removed from ScELIP1-19T by digestion with KpnI and XbalI and cloned into KpnI and XbalI-digested pCAMBIA 1301 to construct a 35S-ScELIP1 gene ( Figure S2). Likewise, the ScELIP2 ORF was removed from ScELIP1-19T by digestion with Bam HI and XbalI and cloned into BamHI and XbalI-digested pCAMBIA 1301 to construct a 35S-ScELIP2 gene ( Figure S3). The pScELIP1-CAMBIA 1301 and pScELIP2-CAMBIA 1301 were introduced separately into an Agrobacterium tumefaciens strain EHA105 by triparental mating as described by Hoekema et al. [48] and introduced into 6-week old Arabidopsis ELIP mutant Atelip plants by the floral dip method [49]. T1 transgenic plants were selected by germination on MS agar plates containing Hygromycin (80 mg/L). After 7 days, the majority of the seedlings turn yellow or white and die. After 10 days, those seedlings that continued to stay green and grow were considered as stable transformants. The stable transformants were verified by PCR by using the same gene-specific primers used to isolate the coding sequences for each ScELIP. Primary transformants were shelfed to generate T2 homozygous transgenic seed stocks for production of T3 homozygous plants used in the phenotypic analysis.

Seed Germination Assay
Petri plates containing 1/2 MS agar media (1%) were divided into four quadrants and approximately 50 seeds were sown of each genotype into separate quadrants: Arabidopsis Col-0 wildtype (WT), the Atelip mutant, and two transgenic Arabidopsis lines of ScELIP1 or ScELIP2. Seed germination, when the radicle protruded through the seed coat, was scored from the first day after sowing. The seed germination assay was conducted under standard conditions (22 ± 2 • C, 14 h light/ 10 h dark cycle, 60-75% relative humidity, and PPFD of 100 µmol/m 2 /s) as a control or under the following treatments; irradiated by red, blue, UVB, or high-light (1000 µmol/m 2 /s) as their single light source (as mentioned in 2.3 Extraction of RNA and RT-qPCR based expression analysis) at 22 • C 14 h light/10 h dark cycle for 6 days.

Phenotypic Analysis of Transgenic A. Thaliana
Sterile WT, Atelip mutant, and ScELIPs transgenic Arabidopsis seeds were vernalized for 2 d and germinated on 1/2 MS agar medium under control conditions of 22 • C and 14 h light/10 h dark cycle and PPFD of 100 µmol/m 2 /s. Seven-day old seedlings, of similar size, were chosen for exposure to experimental treatments. WT, Atelip mutant, and transgenic ScELIPs lines, were cultured on 1/2 MS medium for 7 days at 22 • C 14 h light/10 h dark cycle. Individual light treatments were administered for 7 days at 22 • C 14 h light/10 h dark cycle and PPFD of 100 µmol/m 2 /s under the appropriate light source of either red, blue, or UVB as described for the gene expression study. After all treatments the number of leaves, roots, and the length of the longest root were recorded.
For the high-light treatment, seven-day-old seedling, grown under control conditions of 22 • C and 14 h light/10 h dark cycle and PPFD of 100 µmol/m 2 /s, were briefly exposed to light at an intensity of 1500 µmol/m 2 /s for 2 h and subsequently transferred to normal conditions for 24 h to recover. Following recovery, the seedlings were assessed for chlorophyll content as described in a later section.

High-Light Treatment of Plantlets
Seedlings of WT, Atelip mutant, and ScELIPs transgenic lines of Arabidopsis were grown in 5 cm diameter pots in a peat substrate (Pindstrup, Mosebrug, Ryomgård, Denmark) and grown under well-watered controlled conditions at 22 ± 2 • C with a 14 h light/ 10 h dark cycle, PPFD of 100 µmol/m 2 /s, and 60-75% relative humidity. After four weeks plants were irradiated with high-light (1000 µmol/m 2 /s) at 22 • C 14 h light/10 h dark cycle under well-watered conditions. F v /F m was measured before treatment (0 h), after exposure to high-light for 3 days and then continuously for 3 weeks. Leaf samples were taken for chlorophyll and carotenoid analyses before and after 3 days and 3 weeks of high-light treatment.
The relative transcript abundance was assessed for ScELIP1, ScELIP2, One-Helix Protein (OHP), OHP2, two-helix protein (SEP2), PSII CP29 antenna protein (LHCB4.2), PSI antenna protein (LHCA2), PSII CP22 protein (PSBS), and PSII D2 protein (PSBD), after exposure to high-light for 0 h and 2 h, 3 days and 3 weeks. Each treatment consisted of 3 biological replicates. The method of extraction of RNA and RT-qPCR based expression analysis was as stated previously. To compare relative expression levels, Col-0 WT and all ScELIPs transgenic lines of Arabidopsis were compared to the Atelip mutant, and Atα-TUB was used as a reference gene; primer sequences are listed in Table S3.

Pigment Analysis
Chlorophyll content was measured according to the methods described by Ritchie 2006 [50]. Leaf samples (50 mg Fwt) were collected from three separate plants for each line and at each treatment phase. Pigments were extracted by incubation of the leaf samples in 2 mL of 96% ethanol (room temperature~25 • C) for 4 h in darkness with constant agitation. The extracts were centrifuged at 10,000 rpm for 2 min and the supernatants removed for analysis. Supernatants were analyzed spectrophotometrically at wavelengths of 470, 649, and 665 nm using a UV-Visible spectrophotometer (Biomate 3S, Thermo Fisher Scientific, Waltham, MA, USA). The concentration of the chlorophyll a, b, and total carotenoids were determined using the following equations: Chl a = 13.95 × OD 665 − 6.88 × OD 649 , Chl b = 24.96 × OD 649 − 7.32 × OD 665 , and Car = (1000 × OD 470 -2.05 × Chl a-114.8 × Chl b)/245. The total pigment content in mg/g =N × C × V/W, "N" represents dilution ratio, "C" represents pigments concentration (mg/mL), "V" represents the volume of extracting solution (mL), "W" represents sample fresh weight (g).

Fluorometric Assessment of Photosynthetic Performance
Photosynthetic performance of S. caninervis at a different light intensity and times were assessed by pulse amplitude modulated fluorometry using a portable chlorophyll fluorometer (PAM 2500) (Heinz, Walz, Berlin, Germany). Measurements of chlorophyll fluorescence were recorded in situ on the mid portion of the uppermost fully mature leaf. The saturation pulse method was used to calculate the F v /F m , the parameter settings were based on the recommendations of Zhang et al. [51]. All parameters were measured on 6 individual plants and the values were averaged for each genotype.

Statistical Analyses
All statistical analyses were performed using Statistical Product and Service Solutions (SPSS) 16.0 software (SPSS Inc., Chicago, IL, USA). Data were compared using one-way ANOVA, Dunnett's T3 was used to examine the difference in significance of ANOVA results, and values were considered as significantly statistically different at p < 0.05, or distinctly statistically different at p < 0.01. Error bars represent standard deviations.

Conclusions
In Syntrichia caninervis, ScELIP1 and ScELIP2 transcript abundance were activated by multiple light stresses, especially increasing high-light intensity. Expression of ScELIPs in the Atelip mutant increase germination rates but the rates do not attain WT rates when grown in red, blue, UVB, and high-light conditions. Different light quality changed morphology after the germination and seedling stage, while this phenotype was not altered between Col-0 WT, Atelip mutant, and 35S-ScELIPs transgenic lines. Two ScELIPs can protect chlorophyll and accumulation of photoprotective pigments such as carotenoid under high-light stress. High-light leads to transcriptional suppression of genes encoding antenna proteins such as LHCA2, LHCB4.2, PSBS at 2 h and 3 days, but slightly increases at 3 weeks. High-light causes transcriptional activation of genes encoding proteins responsible for photoprotection, such as ScELIP1 and ScELIP2 and 3 of the AtELIP family (OHP, OHP2, SEP2). These findings can clarify the process of ELIPs of bryophyte response to different light quality and/or intensity especially to high-light and is important for land plant evolutionary adaptation.