The Functional Characterization of MaGS2 and Its Role as a Negative Regulator of Ciboria shiraiana

Glutamine synthetase (GS) is a key enzyme involved in nitrogen metabolism. GS can be divided into cytosolic and plastidic subtypes and has been reported to respond to various biotic and abiotic stresses. However, little research has been reported on the function of GS in mulberry. In this study, the full length of MaGS2 was cloned, resulting in 1302 bp encoding 433 amino acid residues. MaGS2 carried the typical GS2 motifs and clustered with plastidic-subtype GSs in the phylogenetic analysis. MaGS2 localized in chloroplasts, demonstrating that MaGS2 is a plastidic GS. The expression profile showed that MaGS2 is highly expressed in sclerotiniose pathogen-infected fruit and sclerotiniose-resistant fruit, demonstrating that MaGS2 is associated with the response to sclerotiniose in mulberry. Furthermore, the overexpression of MaGS2 in tobacco decreased the resistance against Ciboria shiraiana, and the knockdown of MaGS2 in mulberry by VIGS increased the resistance against C. shiraiana, demonstrating the role of MaGS2 as a negative regulator of mulberry resistance to C. shiraiana infection.


Introduction
Glutamine synthetase (GS; EC6.3.1.2) is a key enzyme involved in nitrogen metabolism, including the assimilation of ammonia deriving from mineral nutrition, biological nitrogen fixation, photorespiration, and amino acid breakdown, which also initially converts inorganic nitrogen from the soil into organic nitrogen through the combined action of glutamate synthase (GOGAT; EC 1.4.1.14and EC 1.4.7.1) in higher plants [1,2].GS has a crucial function in nitrogen metabolism as it catalyzes the assimilation of ammonium from different sources to form glutamine, so it is essential for ammonium assimilation, reassimilation, and cycling [3].In wheat, GS2 is responsible for the reassimilation of NH 4 + generated from photorespiration and the assimilation of NH 4 + derived from NO 3 − reduction [4].Three GS superfamilies (GSI, GSII, and GSIII) have been widely identified in both prokaryotes and eukaryotes based on their gene/protein sequences, protein structure phylogenetic analyses, and their molecular weight.Prokaryotes are more likely to have the isoforms of GSI, while isoforms of GSII are more common in eukaryotes [5][6][7][8].In plants, glutamine synthesis is catalyzed by enzymatic proteins belonging to the GSII superfamily, and two groups of functional GS enzymes have been found: eubacterial GSIIb (GLN2) and eukaryotic GSIIe (GLN1/GS) [6].Phylogenetic studies have classified the different GS genes of seed plants into three clusters: two cytosolic glutamine synthetases, GS1a and GS1b, and chloroplastidic GS2.GS1a was firstly identified in pine and thought to be divergent gymnospermous GS1 [6,9].Since then, GS1a genes have been identified in all gymnosperms, Plants 2024, 13, 1660 2 of 10 basal angiosperms, and some Magnoliidae species, excluding more recent angiosperm species [6].GS2 has also been found in Cycadopsida gymnosperms, suggesting the origin of GS2 in a common ancestor of Cycadopsida, Ginkgoopsida, and angiosperms [2,10].In general, two types of GS isoforms exist in higher plants: cytosolic GS1b, which is also known as GS1, and plastidic GS2.GS1 belongs to a small, multi-gene family; localizes in vascular tissues and roots; and primarily generates glutamine for intercellular nitrogen transport [11,12].GS2, which is encoded by a single gene, is predominantly expressed in green tissues, playing an essential role in the reassimilation of the ammonium released by photorespiration [13].
GS plays a fundamental role in growth and development in plants [5].The GSs in Arabidopsis thaliana and rice were reported to be involved in plant growth and differentiation.The role of GS in senescence had been reported in some species, including Arabidopsis thaliana, rice, wheat, and barley [7].Transgenic poplars with an ectopic expression of pine cytosolic GS exhibited enhanced vegetative growth [14,15].GS-overexpressing rice plants also showed enhanced vegetative growth with higher soluble protein concentrations in their leaves but decreased growth in terms of both grain yield production and total amino acids in their seeds [1].In addition, GS plays important roles in the response to diverse abiotic stresses.A role for cytosolic GS was clearly established in proline production [16].Transgenic poplar with pine cytosolic GS showed enhanced resistance to drought stress [14].In rice, OsGS1;2-overexpressing plants exhibited resistance to Basta selection and higher sensitivity to salt, drought, and cold stress conditions [1].In addition, overexpression of the GS2 in tobacco and rice resulted in enhanced tolerance to photooxidation and to salt stress [17,18].GS was also reported to play a role in rice susceptibility to pathogen infection.A previous study indicated that glutamine is a potential key nutrient during Nitrogen-Induced Susceptibility (NIS), and a mutant of the OsGS1-2 glutamine synthetase gene enhanced plant resistance to Magnaporthe oryzae and abolished NIS [19].
Mulberry (Morus spp., Moraceae) is a traditional economic crop plant with ecological and nutritional value [20].Mulberry sclerotiniose is a devastating fungal disease affecting mulberry fruit quality and yield [21,22]. Ciboria shiraiana is the dominant causal agent of mulberry sclerotiniose in China, and it results in hypertrophy sorosis sclerotiniose, which limits the healthy development of a diversified utilization of mulberry [23].GS genes have been reported to be involved in plant development and resistance to diverse stresses.However, studies on GS in mulberry are few.In the present study, a plastidic subtype of glutamine synthetase MaGS2 was identified in mulberry, and its role in the response to sclerotiniose infectious disease was explored.Finally, MaGS2 was functionally characterized as a negative regulator for resistance to C. shiraiana infection in mulberry.

MaGS2 Is a Plastidic-Subtype Glutamine Synthetase
The coding sequence of the MaGS2 gene was cloned based on the sequence information identified in the mulberry genome database, and the sequence was deposited in GenBank with the accession number OR797682.The bioinformatics analysis showed that the full-length coding sequence of MaGS2 was 1302 bp.MaGS2 encodes a peptide with 433 animo acid residues; a molecular weight of 47.6 kDa; a theoretical PI of 6.8, which means that it is acidic; and an instability index of 41.76 (>40), implying the instability of the encoded protein.The multiple sequences' alignment results showed that MaGS2 shares a 69.85% consensus with GLN1;1, GLN1;2, GLN1;3, GLN1;4, GLN1;5, and GLN2 from Arabidopsis thaliana, as well as OsGS1;1, OsGS1;2, OsGS1;3, and OsGS2 from rice (Oryza Sativa).The motif analysis using the MEME online tool showed that MaGS2 contains eight typical GS conservative motifs of chloroplast-subtype GS instead of the cytosolic subtype (Figure 1A).The phylogenetic analysis showed that GS proteins could be clustered into two subgroups, GS1 (cytosolic) and GS2 (plastidic), and MaGS2 was clustered with PtGS2.1 and PtGS2.2.PtGS2.1 and PtGS2.2 have been characterized as being of the plastidic subtype [11], indicating that MaGS2 is a plastidic-subtype GS (Figure 1B).Further, the multiple sequence Plants 2024, 13, 1660 3 of 10 alignment of amino acid sequences of GSs showed that MaGS2 contains substrate-binding sites (Gly196, Ser256, Asn320, Ser322, Arg385, and Tyr397), as well as other functional sites of typical GS (Figure 2).tains eight typical GS conservative motifs of chloroplast-subtype GS instead of the cytosolic subtype (Figure 1A).The phylogenetic analysis showed that GS proteins could be clustered into two subgroups, GS1 (cytosolic) and GS2 (plastidic), and MaGS2 was clustered with PtGS2.1 and PtGS2.2.PtGS2.1 and PtGS2.2 have been characterized as being of the plastidic subtype [11], indicating that MaGS2 is a plastidic-subtype GS (Figure 1B).Further, the multiple sequence alignment of amino acid sequences of GSs showed that MaGS2 contains substrate-binding sites (Gly196, Ser256, Asn320, Ser322, Arg385, and Tyr397), as well as other functional sites of typical GS (Figure 2).

MaGS2 Locates in the Chloroplast
The prediction of the subcellular localization of MaGS2 by the online tool Plant-mPLoc showed that MaGS2 localizes in the chloroplast or mitochondrion.The subcellular localization results showed that the yellow florescent protein (YFP) signal of the recombinant protein MaGS2-YFP was overlaid with the chloroplast signal (red signal) (Figure 3), which indicates that MaGS2 localizes in the chloroplast, demonstrating that MaGS2 is a chloroplastidic-subtype GS.

MaGS2 Locates in the Chloroplast
The prediction of the subcellular localization of MaGS2 by the online tool Pla mPLoc showed that MaGS2 localizes in the chloroplast or mitochondrion.The subcellu localization results showed that the yellow florescent protein (YFP) signal of the recom nant protein MaGS2-YFP was overlaid with the chloroplast signal (red signal) (Figure which indicates that MaGS2 localizes in the chloroplast, demonstrating that MaGS2 i chloroplastidic-subtype GS.

Transcriptional Characteristics of MaGS2 Are Associated with Sclerotiniose
To understand the response of MaGS2 to sclerotiniose, the relative expression lev of MaGS2 in sclerotiniose-resistant fruit (K), healthy fruit (L), and sclerotiniose-infec fruit (S) were explored.The results showed that the expression level of MaGS2 was mu higher in S than in L and K, and the expression level in K was higher than that in L (Fig 4A ).It is obvious that MaGS2 showed a positive response to sclerotiniose.Among the  Gly196, Ser256, Asn320, Ser322, Arg385, and Tyr397 are associated with substrate-binding sites and are highlighted in blue.Arg380 and Arg401 are associated with the phosphate transfer reaction and are highlighted in red.Tyr288, Glu291, and Arg292 are involved in hydrophobic interactions between subunits and are highlighted in green.Glu198, Glu200, Glu261, Glu268, His318, and Glu399 are involved in cationic coordination and are highlighted in yellow.Glu366 and Asp116 are involved in the assimilation of NH4 + and are highlighted in purple.

MaGS2 Locates in the Chloroplast
The prediction of the subcellular localization of MaGS2 by the online tool Plant-mPLoc showed that MaGS2 localizes in the chloroplast or mitochondrion.The subcellular localization results showed that the yellow florescent protein (YFP) signal of the recombinant protein MaGS2-YFP was overlaid with the chloroplast signal (red signal) (Figure 3), which indicates that MaGS2 localizes in the chloroplast, demonstrating that MaGS2 is a chloroplastidic-subtype GS.

Transcriptional Characteristics of MaGS2 Are Associated with Sclerotiniose
To understand the response of MaGS2 to sclerotiniose, the relative expression levels of MaGS2 in sclerotiniose-resistant fruit (K), healthy fruit (L), and sclerotiniose-infected fruit (S) were explored.The results showed that the expression level of MaGS2 was much higher in S than in L and K, and the expression level in K was higher than that in L (Figure 4A).It is obvious that MaGS2 showed a positive response to sclerotiniose.Among the tissues, including the stem, leaf, xylem, phloem, and fruits at four different development stages (F-S0, F-S1, F-S2, F-S3), MaGS2 was highly expressed in the leaf, F-S0, and F-S1 and barely expressed in the xylem, phloem, stem, F-S2, and F-S3 (Figure 4B).The expression level of MaGS2 decreased with the development of the fruit.These results indicate that MaGS2 is preferentially expressed in the leaf and unripe mulberry fruits.

Transcriptional Characteristics of MaGS2 Are Associated with Sclerotiniose
To understand the response of MaGS2 to sclerotiniose, the relative expression levels of MaGS2 in sclerotiniose-resistant fruit (K), healthy fruit (L), and sclerotiniose-infected fruit (S) were explored.The results showed that the expression level of MaGS2 was much higher in S than in L and K, and the expression level in K was higher than that in L (Figure 4A).It is obvious that MaGS2 showed a positive response to sclerotiniose.Among the tissues, including the stem, leaf, xylem, phloem, and fruits at four different development stages (F-S0, F-S1, F-S2, F-S3), MaGS2 was highly expressed in the leaf, F-S0, and F-S1 and barely expressed in the xylem, phloem, stem, F-S2, and F-S3 (Figure 4B).The expression level of MaGS2 decreased with the development of the fruit.These results indicate that MaGS2 is preferentially expressed in the leaf and unripe mulberry fruits.

MaGS2 Negatively Regulates Resistance against Ciboria shiraiana Infection
To understand the influence of MaGS2 on resistance against the sclerotiniose pathogen C. shiraiana, transient MaGS2-overexpressing tobaccos lines were obtained; then, the leaves of the transient MaGS2-overexpressing tobacco were inoculated with a PDA disc culture of C. shiraiana.The results showed that MaGS2 was truly and significantly overexpressed in the treated tobacco leaves (Figure 5A).The OE-MaGS#T6 leaf was fully damaged with cell death symptoms, and the damaged area of OE-MaGS#T7 was much larger than that of the control 4 days after inoculation.In addition, sclerotium (indicated by red circles) appeared on OE-MaGS2#T6 prior to the control.The cell death symptoms of OE-MaGS2#T7 were even more severe when compared with those of the control 8 days after inoculation (Figure 5B).

MaGS2 Negatively Regulates Resistance against Ciboria shiraiana Infection
To understand the influence of MaGS2 on resistance against the sclerotiniose pathogen C. shiraiana, transient MaGS2-overexpressing tobaccos lines were obtained; then, the leaves of the transient MaGS2-overexpressing tobacco were inoculated with a PDA disc culture of C. shiraiana.The results showed that MaGS2 was truly and significantly overexpressed in the treated tobacco leaves (Figure 5A).The OE-MaGS#T6 leaf was fully damaged with cell death symptoms, and the damaged area of OE-MaGS#T7 was much larger than that of the control 4 days after inoculation.In addition, sclerotium (indicated by red circles) appeared on OE-MaGS2#T6 prior to the control.The cell death symptoms of OE-MaGS2#T7 were even more severe when compared with those of the control 8 days after inoculation (Figure 5B).
Inoculation with a PDA disc culture of C. shiraiana was also performed using mulberry leaves.The qRT-PCR results showed that the expression level of MaGS2 was significantly knocked down by VIGS (virus-induced gene silencing) (Figure 5C).When inoculated with a disk culture of C. shiraiana, the damaged areas on MaGS2-knockdown leaves were smaller than those on control leaves 4 days after inoculation.Furthermore, sclerotium appeared on the control leaves 8 days after inoculation (Figure 5D).Altogether, these results indicate that MaGS2 is a negative regulator of resistance against C shiraiana infection.

Discussion
Being an indispensable member of the GS-GOGAT cycle, through which plants complete approximately 95% of their NH4 + assimilation, GS plays pivotal roles in overall N flow across the living system [7].GS is encoded by a small family of nuclear genes.GS1 is encoded by several functional redundancy genes and usually locates in the cytosol, while GS2 is encoded by a single nuclear gene, targets the chloroplast, and is larger than GS1 in terms of its molecular weight [3,7].In the present study, the GS2 gene in mulberry was explored.MaGS2 contains a conserved domain similar to that of GS2 in Arabidopsis thaliana Inoculation with a PDA disc culture of C. shiraiana was also performed using mulberry leaves.The qRT-PCR results showed that the expression level of MaGS2 was significantly knocked down by VIGS (virus-induced gene silencing) (Figure 5C).When inoculated with a disk culture of C. shiraiana, the damaged areas on MaGS2-knockdown leaves were smaller than those on control leaves 4 days after inoculation.Furthermore, sclerotium appeared on the control leaves 8 days after inoculation (Figure 5D).Altogether, these results indicate that MaGS2 is a negative regulator of resistance against C shiraiana infection.

Discussion
Being an indispensable member of the GS-GOGAT cycle, through which plants complete approximately 95% of their NH 4 + assimilation, GS plays pivotal roles in overall N flow across the living system [7].GS is encoded by a small family of nuclear genes.GS1 is encoded by several functional redundancy genes and usually locates in the cytosol, while GS2 is encoded by a single nuclear gene, targets the chloroplast, and is larger than GS1 in terms of its molecular weight [3,7].In the present study, the GS2 gene in mulberry was explored.MaGS2 contains a conserved domain similar to that of GS2 in Arabidopsis thaliana (Figure 2) and localizes in the chloroplast (Figure 3), indicating that MaGS2 belongs to the plastidic subtype of GS.These results are consistent with results obtained for Arabidopsis thaliana and wheat [3,4,7].Studies on plastidic GS (GS2) have been reported in many seed plants and have mainly focused on its roles in plant development and in response to abiotic stresses [7,13].In other studies, GSs were reported to mitigate the effects resulting from a range of abiotic stresses, including cold, salt, drought, light, NH 4 + toxicity, H 2 O 2 treatment, wounding, ultraviolet B radiation, heat, and oxidative stress in plant systems [7].Few studies have focused on its role in response to biotic stresses.In this study, the MaGS2 gene was characterized as being involved in a to biotic stress.Additionally, the expression pattern of MaGS2 showed tissue and development stage expression preferences, which indicates that MaGS2 is involved in mulberry fruit development and biotic stress mediation (Figure 4AB).Furthermore, the tissues with a high expression level of MaGS2 are also rich in chloroplasts; this could be explained by its function in the development and degeneration of chloroplasts.Mutants lacking plastidic GS are conditionally lethal, and the knockdown of GS delays DNA repair and nucleotide metabolism in both in vivo and in vitro animal systems [13,24].The nitrogen supply strongly affects rice blast susceptibility but only slightly affects plant growth [19].The occurrence of Nitrogen-Induced Susceptibility (NIS) implies the possible role of GS in affecting resistance to biotic stresses.In rice, a mutant of the glutamine synthetase OsGS1-2 gene enhances plant resistance to M. oryzae and abolishes NIS [19].In Arabidopsis thaliana, gln2 mutants had been speculated to be lethal, but a recent study revealed that gln2-knockout mutants were viable and did not show any aberrant phenotypes in air or high CO 2 [25].However, the role of GS2 in regulating resistance to pathogen infections is still unknown.The current work identified the MaGS2 gene in mulberry, and its expression level was significantly induced by sclerotiniose infection (Figure 4A).As reported in many plant species, GS1 is mainly expressed in roots and vascular tissues, while plastidic GS2 has an expression preference in leaves, which corresponds to its chloroplast localization [5,11,12,26].MaGS2, which was determined to locate in chloroplasts, also showed its highest expression level in the leaf in mulberry.Interestingly, MaGS2 also showed a high expression level in immature fruits at early developmental stages.It is known that the fruit ripening process occurs along with the deterioration of chloroplasts [27,28].The decreased expression level of MaGS2 is consistent with the decay of chloroplasts.Given that outbreaks of sclerotiniose diseases mainly occur at the early development stage of mulberry fruits, the expression pattern of MaGS2 in developmental fruits and diseased fruits suggests its possible role in response to sclerotiniose pathogen infection.In the present study, the transient overexpression of MaGS2 in tobacco decreased resistance against C. shiraiana, and the plant resistance decreased with an increased expression level of MaGS2 (Figure 5A).The knockdown of MaGS2 in mulberry increased resistance against C. shiraiana (Figure 5D).Both the overex-pression and knockdown of MaGS2 suggest that MaGS2 works as a negative regulator of mulberry resistance to C. shiraiana.Therefore, it is likely that MaGS2, like the OsGS1-2 gene in rice, regulates mulberry resistance to fungal pathogens through NIS.Further studies should be carried out to underline the NIS mechanism regulated by GS2 in mulberry.

Plant Materials
Mature, healthy purple fruits (L) from cultivar Zhongshen No.1, sclerotiniose-infected fruits (S) from cultivar Zhongshen No.1 with the typical symptom (milky-white swollen fruit) of hypertrophy sorosis sclerotiniose, and mature healthy fruits from the sclerotinioseresistant cultivar K were used to detect the response of MaGS2 to sclerotiniose.Mulberry fruits in different development stages, including inflorescence (F-S0), green fruits (F-S1), reddish fruits (F-S2), and mature purple fruits (F-S3), and different tissues, including stem, leaf, phloem, and xylem, all from the cultivar Zhongshen No.1, were used to explore the expression profile of the MaGS2 gene.All the plant materials were collected from National Mulberry Gene Bank (NMGB), Zhenjiang, China.All the plant tissues and organs were frozen immediately with liquid nitrogen and kept in a −80 • C ultra-low-temperature refrigerator until use.
Mulberry seedlings for VIGS assay and tobacco seedlings for transient overexpression were cultured in a growth chamber at 28 • C for 16 h under light and 26 • C for 8 h under dark conditions.

RNA Extraction and cDNA Synthesis
Plant materials were ground into powder under liquid nitrogen.The total RNA was extracted following the instructions of the easyspin Plus Plant RNA extraction toolkit (RN38) (Aidlab, Beijing, China).The RNA quality and concentration were detected by agarose gel electrophoresis and a NanoDrop One nucleic acid micro detector (Thermo Scientific, Waltham, MA, USA), respectively.cDNA was synthetized following the instructions of the Hiscript III RT supermix for qPCR toolkit (Vazyme, Nanjing, China) with 1 µg RNA.

Transcriptional Characteristics of MaGS2
The transcriptional characteristics of the MaGS2 gene were obtained by qRT-PCR with the ABI StepOnePlus™ Real-Time PCR System (Foster City, CA, USA).The expression levels of the MaGS2 gene in the fruit of sclerotiniose-resistant cultivar K (K), healthy fruit of cultivar Zhongshen No.1 (L), and sclerotiniose-infected fruit of cultivar Zhongshen No.1 (S) were detected to understand the response of MaGS2 to sclerotiniose.The expression levels of MaGS2 in tissues, including the stem, leaf, xylem, phloem, and fruits in four development stages (F-S0, F-S1, F-S2, F-S3), were detected to understand the expression preference of MaGS2.The specific primers for qRT-PCR were designed with Primer Premier 6.0 software and the Primer-BLAST online tool (https://www.ncbi.nlm.nih.gov/tools/primer-blast/index.cgi(accessed on 12 December 2023)) and were named MaGS2-QF and MaGS2-QR (sequences of primers, MaGS2-QF: CCTCCGCCACAAAGAGCATA, MaGS2-QR: TGAGGTCACGATGTAGGGGT).A qRT-PCR mixture containing chamQ SYBR qPCR Master Mix (High ROX Premixed) (Vazyme, Nanjing), 0.5 µM of each specific primer, and appropriate cDNA diluted with DEPC-treated ddH 2 O was prepared with a total volume of 10 µL.A two-step thermal cycling protocol (95 • C for 30 s, followed by 40 cycles of 95 • C for 5 s and 60 • C for 30 s) was adopted to perform the qRT-PCR.MaActin (primers: MaActin-QF and MaActin-QR) was used as an internal reference [30], and the relative expression levels of the MaGS2 gene were computed with the 2 −∆Ct method.

Subcellular Localization of MaGS2
Before the experiments were carried out, the subcellular localization of MaGS2 was predicted by the online tool Plant-mPLoc (http://www.csbio.sjtu.edu.cn/bioinf/plantmulti/(accessed on 14 December 2023)) as the requirement of the developer [31].The full-length coding sequence of MaGS2 without the terminal codon was cloned into a pBI121 vector containing the YFP gene between the recognition sites of BamH I and Xba I by seamless cloning.Then, the recombinant plasmids were transformed into the E. coli DH5α strain, followed by sequencing by SUNYA biotechnology company.The correct recombinant plasmids were transformed into the Agrobacterium tumefaciens GV3101 strain.The transformant was cultured at 28 • C and 200 rpm with liquid LB medium containing 50 µg/mL kanamycin and rifampicin until the OD 600 reached approximately 0.6.The culture was collected by centrifugation at 6000 rpm for 6 min.Then, the sediment pellets were resuspended with infiltration medium (10 mm MES monohydrate pH 5.6, 10 mm MgCl 2 , 200 µM acetosyringone, 400 mg/L L-Cysteine, 5 mL/L Tween-20, 50-500 µL/L Silwet L-77, 5% sucrose) and kept still for 3 h at 28 • C, after which they were infiltrated into Nicotina benthamiana leaves.The leaves were harvested after 48 h, and the fluorescence signal was observed by a Leica TCS SP8 confocal microscope.

Overexpression and VIGS of MaGS2 Followed by C. shiraiana Infection
MaGS2 was cloned into a pNC-Cam1304-MCS35S plasmid vector by seamless cloning and transformed into A. tumefaciens GV3101 competent cells.The transformant was cultured at 28 • C and 200 rpm with liquid LB medium containing 50 µg/mL kanamycin and rifampicin until the OD 600 reached approximately 0.6.The culture was collected and then resuspended with infiltration medium as described above.After stewing at 28 • C for 4 h in darkness, the infiltration medium containing the transformants was subsequently infiltrated into the leaf of N. benthamiana, and A. tumefaciens containing empty pNC-Cam1304-MCS35S vector was used as a control.The tobacco was kept in darkness for 48 h, then cultivated in a growth chamber under general conditions.The leaves of the treated tobacco were harvested after 3 days, and the leaves were cut into two halves along the vein for qRT-PCR and C. shiraiana infection experiments.
For VIGS assay, the best interfering region was predicted by the SGN VIGS Tool online tool (https://vigs.solgenomics.net(accessed on 13 December 2023)), and then the best interfering region was cloned into the pNC-TRV2-GFP vector by seamless cloning, followed by transformation into A. tumefaciens GV3101 strain competent cells.The transformant was cultivated, collected, and resuspended as described above.A 1:1 mixture of A. tumefaciens containing pNC-TRV2-GFP-MaGS2 and pTRV1 was infiltrated into the leaves of 4-week-old mulberry seedlings of cultivar Fengchi under vacuum (−0.4 to −0.6 kg/cm 2 ) conditions for 4 min.A 1:1 mixture of A. tumefaciens containing pNC-TRV2-GFP empty vector and pTRV1 was used as a control.The treated mulberry seedlings were kept in darkness for 24 h, then cultivated under general conditions in a growth chamber.The leaves of the treated mulberry seedlings were harvested after 23 days, and the leaves were cut into two halves along the vein for qRT-PCR and C. shiraiana infection experiments.
C. shiraiana was cultivated on potato dextrose agar medium (Coolaber, Beijing) at 26 • C for 4-5 days, then cut into small discs and put on lightly wounded half-leaves that had been sterilized with 75% ethanol for 2 min and washed with ddH 2 O.The damaged areas with cell death symptoms caused by infection and the appearance of sclerotia were observed and recorded.

Figure 2 .
Figure 2. Multiple sequence alignment of MaGS2 and GSs from Arabidopsis thaliana and Oryza satGly196, Ser256, Asn320, Ser322, Arg385, and Tyr397 are associated with substrate-binding sites are highlighted in blue.Arg380 and Arg401 are associated with the phosphate transfer reaction are highlighted in red.Tyr288, Glu291, and Arg292 are involved in hydrophobic interactions tween subunits and are highlighted in green.Glu198, Glu200, Glu261, Glu268, His318, and Glu are involved in cationic coordination and are highlighted in yellow.Glu366 and Asp116 are invol in the assimilation of NH4 + and are highlighted in purple.

Figure 3 .
Figure 3. Subcellular localization of MaGS2.The red signal indicates chloroplasts, and the YFP nal overlays with the red signal, indicating that MaGS2 locates in the chloroplast.

Figure 2 .
Figure 2. Multiple sequence alignment of MaGS2 and GSs from Arabidopsis thaliana and Oryza sativa.Gly196, Ser256, Asn320, Ser322, Arg385, and Tyr397 are associated with substrate-binding sites and are highlighted in blue.Arg380 and Arg401 are associated with the phosphate transfer reaction and are highlighted in red.Tyr288, Glu291, and Arg292 are involved in hydrophobic interactions between subunits and are highlighted in green.Glu198, Glu200, Glu261, Glu268, His318, and Glu399 are involved in cationic coordination and are highlighted in yellow.Glu366 and Asp116 are involved in the assimilation of NH 4 + and are highlighted in purple.

Figure 2 .
Figure 2. Multiple sequence alignment of MaGS2 and GSs from Arabidopsis thaliana and Oryza sativa.Gly196, Ser256, Asn320, Ser322, Arg385, and Tyr397 are associated with substrate-binding sites and are highlighted in blue.Arg380 and Arg401 are associated with the phosphate transfer reaction and are highlighted in red.Tyr288, Glu291, and Arg292 are involved in hydrophobic interactions between subunits and are highlighted in green.Glu198, Glu200, Glu261, Glu268, His318, and Glu399 are involved in cationic coordination and are highlighted in yellow.Glu366 and Asp116 are involved in the assimilation of NH4 + and are highlighted in purple.

Figure 3 .
Figure 3. Subcellular localization of MaGS2.The red signal indicates chloroplasts, and the YFP signal overlays with the red signal, indicating that MaGS2 locates in the chloroplast.

Figure 3 .
Figure 3. Subcellular localization of MaGS2.The red signal indicates chloroplasts, and the YFP signal overlays with the red signal, indicating that MaGS2 locates in the chloroplast.

Plants 2024 , 11 Figure 4 .
Figure 4. Expression profiles of MaGS2.(A) The expression levels of MaGS2 in sclerotiniose-resistant fruit (K), healthy fruit (L), and sclerotiniose-infected fruit (S).(B) The expression levels of MaGS2 in the stem, leaf, xylem, phloem, and fruits at different development stages (F-S0~F-S3).The same letter in lower case indicates no significant difference, while different letters indicate significant differences.

Figure 4 .
Figure 4. Expression profiles of MaGS2.(A) The expression levels of MaGS2 in sclerotiniose-resistant fruit (K), healthy fruit (L), and sclerotiniose-infected fruit (S).(B) The expression levels of MaGS2 in the stem, leaf, xylem, phloem, and fruits at different development stages (F-S0~F-S3).The same letter in lower case indicates no significant difference, while different letters indicate significant differences.Plants 2024, 13, x FOR PEER REVIEW 6 of 11