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Genes 2013, 4(2), 264-274; doi:10.3390/genes4020264
Published: 30 May 2013
Abstract: The Scribble protein complex genes, consisting of lethal giant larvae (Lgl), discs large (Dlg) and scribble (Scrib) genes, are components of an evolutionarily conserved genetic pathway that links the cell polarity in cells of humans and Drosophila. The tissue expression and developmental changes of the Scribble protein complex genes were documented using qRT-RCR method. The Lgl and Scrib genes could be detected in all the experimental tissues, including fat body, midgut, testis/ovary, wingdisc, trachea, malpighian tubule, hemolymph, prothoracic gland and silk gland. The Dlg gene, mainly expressed only in testis/ovary, could not be detected in prothoracic gland and hemolymph. In fat body, there were two higher expression stages of the three genes. The highest peak of the expression of the Lgl and Scrib genes in wingdisc lay at the 1st day of the 5th instar, but the Dlg gene was at 3rd day of 5th instar. The above results indicate that Scribble complex genes are involved in the process of molting and development of the wingdisc in the silkworm. This will be useful in the future for the elucidation of the detailed biological function of the three genes Scrib, Dlg and Lgl in B. mori.
During development of an organism, cells exhibit different shapes from columnar epithelial cells to stellate fibroblast cells, and cell shape plays an important role for maintenance of normal cellular functions and tissue homoeostasis . Cell polarity is important for cell shape maintenance, which is generally described as the asymmetric distribution of cellular constituents, and this includes membrane proteins, carbohydrates and lipids . Loss of cell polarity in epithelium is commonly linked to cancer development and progression .
The Scribble protein complex were identified first in Drosophila as cell polarity genes consisting of lethal giant larvae (Lgl), discs large (Dlg) and scribble (Scrib), which are evolutionarily conserved components of a common genetic pathway that link the disparate functions of cell polarity and cell proliferation in epithelial cells . Mutants of all three genes can induce the development of multilayered and invasive tumors in Drosophila imaginal epithelia, which are called “neoplastic” tumor-suppressor genes . Intriguingly, the neoplastic tumor-suppressor mutants do not overproliferate when surrounded by wild-type tissue; instead, these mutant clones are eliminated from epithelium by cell competition . Scrib gene encodes a membrane associated scaffolding protein, which contains 16N-terminal leucine-rich repeats (LRRs) and four PDZ domains (a member of the LAP family protein) . Dlg as a scaffolding protein of the MAGUK family contains three PDZ domains, an SH3 domain, and a GUK domain . Compared to Scrib and Dlg, Lgl is not a scaffolding protein but a WD40 repeat protein . Scrib localizes to the adherens junction (AJ) at the basolateral region. Dlg binds to Scrib directly and is situated the same site with Scrib. The Lgl can localize to the plasma membrane after phosphorylation . The Scrib, Dlg,and Lgl proteins are highly conserved in sequence among species, and are likely to be functionally conserved as well. In addition, mammalian Dlg can rescue the phenotype of a Drosophila Dlg mutant . After the complete genome of B. mori was sequenced , the gene expression and regulation was widely analyzed [13,14,15]. However, there are no reports about the genes encoding the Scribble protein complex; including Scribble (Scrib), Discs large (Dlg) and Lethal giant larvae (Lgl) are found in silkworm, B. mori.
In the present research, the Scribble protein complex genes (Scrib, Dlg and Lgl) encoding the Scribble protein complex were identified from the silkworm, B. mori. The tissue expression and developmental change of these three genes were studied.
2. Materials and Methods
The silkworm larvae (P50 strain) were provided by The Sericultural Research Institute, Chinese Academy of Agricultural Sciences. They were reared with mulberry leaves in the laboratory at 25 °C under 14 h light/10 h dark cycles . The different tissues, including fat body (FB), midgut (MT), testis/ovary (TE/OV), wingdisc (WD), trachea (TR), malpighian tubule (MG), hemolymph (HA), prothoracic gland (PG), and silk gland (SG), were dissected in 0.75% NaCl, and stored at −80 °C until use. Based on the molting of larvae of silkworm, the larvae after the 3rd molting to 4th molting were staged as the 4th instar; the larvae after the 4th molting to wandering stage were staged as the 5th instar; the wandering stage larvae were those that had ceased feeding. To analyze the developmental expression pattern of the three genes, the tissues from 10 silkworms were dissected and mixed as one sample.
2.2. Gene Identification
The Scribble complex genes in B. mori were searched in the SilkDB . We used the highly conserved Scrib (GenBank AF190774.2), Dlg (GenBank M73529.1) and Lgl (GenBank NM_164349.3) genes of D. melanogaster as queries to search and identify silkworm Scrib, Dlg and Lgl genes by local BLASTP, with an E-value threshold of 10−6. The identified putative Scrib, Dlg and Lgl genes were validated by search of the protein database of the NCBI. The putative Scrib, Dlg and Lgl genes were also confirmed the sequences found in SilkDB by sequencing the related PCR products. Each gene was further analyzed by the program Pfam to identify its domains (Figure 1).
2.3. RNA Isolation, cDNA Synthesis
Total RNA was isolated from the different tissues of B. mori according to the manufacturer’s protocol of TRIzol® Reagent kit (Ambion, TX, USA). Different tissue samples were homogenized with at least 1ml TRNzol Reagent in the glass homogenizer. The process of total RNA extraction and purification was carried out following the instructions including a DNase treatment. The quality of RNA was ascertained by the spectrophtometric method with an A260/A280 ratio from 1.8 to 2.0 and 1% agarose gels electrophoresis based on the integrity of 18S and 28S rRNA bands. Finally the tolal RNA was dissolved in 30 μL DEPC treated H2O and stored at −80 °C.
The cDNA were synthesized from 2 μg DNase treated total RNA using the M-MLV RTase cDNA Synthesis Kit (Takara, China) with the oligo(dT)18 primers in a 20 μL final volume according to the manufacturer’s protocol. The cDNAs were diluted 10 times and utilized to qRT-RCR experiment.
The qRT-RCR was performed on IQ5 Real-Time qPCR Detection System (Bio-Rad,USA) with SYBR green (Toyobo, Janpan) as dsDNA binding dyes. qRT-PCR reactions were carried out with 2 μL diluted cDNA, 10 μL SYBR® Green Realtime PCR Master Mix, 0.8 μL 10 μΜ upstream primer and downstream primer and 6.4 μL ddH2O in a final volume of 20 μL in triplicate. The reaction was initially denatured at 95 °C for 30 s, followed by 40 cycles of denaturation at 95 °C for 5 s and annealing at 58 °C for 10 s. Melt curve analysis was performed at the end of each PCR thermal profile to assess the specificity of amplification. The primers used in this study were designed by Primer 5.0 software (Table 1).
|Table 1. The primers used for qRT-PCR.|
|Scrib||Scrib F||5' TAGTTCAGCAACTGGAACGC 3'||BGIBMGA005373|
|Scrib R||5' TTCTAGCCATGCGAATTGAG 3'|
|Dlg||Dlg F||5' AACGCTGACGGAGAAATCTT 3'||BGIBMGA010382|
|Dlg R||5' GAGTGTACGCGATCGTCAAT 3'|
|Lgl||Lgl F||5' TCGTCTTCCGAATTACAACG 3'||BGIBMGA005570|
|Lgl R||5' GGCACCTCTTCCTTATGCTC 3'|
|Rp49||Rp49 F||5' CAGGCGGTTCAAGGGTCAATAC 3'||AY769302|
|Rp49 R||5' TGCTGGGCTCTTTCCACGA 3'|
2.5. Tissue-Specific Distribution and Developmental Expression of Scrib, Dlg and Lgl
The distribution of Scrib, Dlg and Lgl mRNAs was detected in fat body (FB), midgut (MT), testis/ovary (TE/OV), wingdisc (WD), trachea (TR), malpighian tubule (MG), hemolymph (HA), prothoracic gland (PG), and silk gland (SG) by qRT-PCR. The qRT-PCR primers are listed in Table 1. The specificity of pairs of primers was verified via the single amplification with expected size in normal PCR amplification and the only peak of the melt curve line in qRT-PCR reactions. qRT-PCR data were obtained as Ct. The mRNA expression of Scrib, Dlg and Lgl was normalized to the RP49 gene for the tissue distribution. Based on the tissue distribution analysis, the developmental expression of Scrib, Dlg and Lgl in fat body and wingdisc was carried out.
3.1. Tissue-Specific Distribution and Developmental Expression of the Scrib Gene
The mRNA expression patterns of the Scrib gene in different tissues of 2nd day of the 5th instar larval of silkworm were determined by qRT-PCR analysis (Figure 2). Our result showed that the Scrib gene is expressed in all the experimental tissues. The highest transcript levels of the Scrib gene was detected in wingdisc, and the next was in testis/ovary. Trachea and hemolymph also showed higher expression level. Malpighian tubule and silk gland showed lower level of the Scrib gene, with 0.27 and 0.23 fold compared to the Rp49 gene.
In insects, the fat body is the central organ for energy metabolism and nutrient storage; it senses and integrates environmental signals such as nutrition and the molting hormone to regulate insect body growth. Therefore, we further detected the developmental expression profile of the Scrib gene in fat body of B. mori. From the 4th day of the 4th instar larval to the 1st day of the 5th instar, the Scrib gene kept higher expression, and then declined to a low level dramatically. During the middle stage of the 5th instar, the Scrib gene increased slightly. After the wandering phase, the Scrib gene increased again (Figure 3).
Because the Scrib gene is expressed mainly in wingdisc (Figure 2), the developmental expression of Scrib mRNA was further analyzed (Figure 4). The Scrib gene showed the highest level from the molting stage of 4th instar to the 1st day of the 5th instar larval, but kept a low level at other stages. These results thus indicated that the Scrib may play a key role during the molting of 4th instar.
3.2. Tissue-Specific Distribution and Developmental Expression of Dlg Gene
The mRNA expression patterns of Dlg gene in different tissues of the 2nd day 5th instar larval of silkworm were determined by qRT-PCR analysis (Figure 5). The Dlg gene expressed mainly in the testis/ovary, being 1.55 fold that of the Rp49 gene. The Dlg gene can also be detected in fat body, trachea, silk gland, midgut and malpighian tubule. The Dlg mRNA was not detected in the prothoracic gland or hemolymph (Figure 5).
The Dlg mRNA in fat body reached the peak level at the 4th day of the 4th instar larval; and then, declined continually to the wandering stage. After pupation, the Dlg expression in fat body increased again (Figure 6).
The Dlg gene in wingdisc kept an increasing pattern from the end of the 4th instar to the 1st day of the 5th instar, and showed the highest level at the 3rd day of the 5th instar. Then, the Dlg gene expression declined significantly and kept a low level before pupation. After pupation, the Dlg expression in fat body increased again (Figure 7).
3.3. Tissue-Specific Distribution and Developmental Expression of Lgl Gene
The Lgl gene expressed in all the experimental tissues. The highest transcript levels of Lgl gene was detected in the prothoracic gland, and the next highest was in the wingdisc. Testis/ovary also showed higher expression levels. The other six tissues showed very low levels of Lgl gene compared to the Rp49 gene (Figure 8).
The Lgl gene in fat body kept a stable low level from the 2nd to 4th instar, then, reached a relative higher peak at the 4th day of 4th instar. From the molting stage of 4th instar to the wandering stage, the Lgl gene in fat body maintained low expression. After pupation, the Lgl expression in fat body increased again (Figure 9), which is similar to the patterns of Scrib and Dlg gene in fat body.
The Lgl gene in wingdisc changed discontinuously from the 3rd day of the 4th instar to pupae. During the two molting stages, from 4th instar to the 5th and from the 5th instar to pupation, the Lgl gene showed a relatively higher level. The Lgl gene expressed highest at the 1st day of the 5th instar larva (Figure 10). After pupation, the Lgl in wingdisc kept a low level, which was different to that in fat body.
In the present study, the tissue distribution and development expression of the Scribble complex genes (Scrib, Dlg and Lgl) in B. mori were performed. To date, there have been no reports about the tissue distribution of Scrib and Dlg genes in insects. Only the tissue distribution of the Lgl genes in Drosophila melanogaster has been reported in previous research . In our results, The Lgl gene mainly expressed in prothoracic gland, wingdisc and testis/ovary in B. mori, can also be detected in fat body, midgut, trachea, malpighian tubule, hemolymph and silk gland, and these showed some difference in the distribution with D. melanogaster. Western blot analysis showed that the Lgl gene mainly expressed in brain and wingdisc, the expression in fat body was weaker, but could not be detected in midgut and hemolymph in D. melanogaster . The difference of the Lgl distribution between two insects might be attributed to that the qRT-RCR used in the present research is more sensitive than Western blotting.
The development expressions of the three genes of Scribble complex (Scrib, Dlg and Lgl) of B. mori in the two tissues were different to each other. Although the expression level of the three genes in fat body were different, the two higher expression stages were similar, one was in the stage from the 4th day of the 4th instar to the 1st day of the 5th instar, the other was the 1st day after pupation. The two stages are relative to the molting of the silkworm, which indicated that the three genes of Scribble complex in fat body may play some important roles in the silkworm molting process. The developmental profiles of the three genes in wingdisc were different to that in the fat body. The highest peak of the expression of Lgl and Scrib gene in wingdisc lay at the 1st day of the 5th instar, but the Dlg gene was at the 3rd day of the 5th instar. There was a relatively higher expression peak to the Dlg gene in the wingdisc after pupation, but the Lgl and Scrib genes kept a low expression at this stage. The above differences indicated that the three genes may play different roles in the wingdisc in silkworm. The expression profiles related to the function of genes, but the function of the three genes of Scribble complex (Scrib, Dlg and Lgl) in B. mori still remains unclear, and the further research about the function is necessary in the future.
Within the experimental tissues, The Scrib, Dlg and Lgl mainly expressed in the testis/ovary, wingdisc, and prothoracic gland in B. mori, respectively. There were two relatively higher expression stages of the three genes in fat body of B. mori. The highest peak of the expression of the Lgl and Scrib genes in wingdisc lay at the 1st day of the 5th instar, but the Dlg gene was at the 3rd day of the 5th instar.
This study is supported by the National Natural Science Foundation of China (31072091, 31272111), and the Funds for Creative Research Groups of Hefei University of Technology.
Conflict of Interest
The authors declare no conflict of interest.
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