Shaohua Wang (1447912), Zhengying You (1447909), Mao Feng (219611), Jiaqian Che (1447918), Yuyu Zhang (1447915), Qiujie Qian (1447921), Setsuko Komatsu (422175), Boxiong Zhong (431919)
{"title":"Analyses of the\\nMolecular Mechanisms Associated with\\nSilk Production in Silkworm by iTRAQ-Based Proteomics and RNA-Sequencing-Based\\nTranscriptomics","authors":"Shaohua Wang (1447912), Zhengying You (1447909), Mao Feng (219611), Jiaqian Che (1447918), Yuyu Zhang (1447915), Qiujie Qian (1447921), Setsuko Komatsu (422175), Boxiong Zhong (431919)","doi":"10.1021/acs.jproteome.5b00821.s007","DOIUrl":null,"url":null,"abstract":"Silkworm\\nis used as a model organism to analyze two standard complex\\ntraits, which are high and low silk yields. To understand the molecular\\nmechanisms of silk production, the posterior silk glands aged to the\\nthird day of the fifth instar were analyzed from the ZB strain with\\nlow silk production and from the control strain Lan10. Using isobaric\\ntags for relative and absolute quantification (iTRAQ) quantitative\\nshotgun proteomics and RNA-sequencing-based transcriptomics, 139 proteins\\nand 630 transcripts were identified as novel in the ZB strain compared\\nwith the Lan10 strain, indicating that these results significantly\\nexpand the coverage of proteins and transcripts of the posterior silk\\nglands in the silkworm. Of the 89 differently changed proteins, 23\\nwere increased, and 66 were decreased. Of the 788 transcripts, 779\\nwere upregulated, and 9 were downregulated. These results confirm\\nthat decreased energy utilization/protein translation and enhanced\\nprotein degradation are the key factors in lower silk production.\\nMoreover, this study provides novel insight into the molecular changes\\nthat may result in lower silk production, namely, a combination of\\nimpaired transcription activity, missed protein folding/transport,\\nand lowered yields of the main components of fibroin, along with weakened\\ngrowth/development of the posterior silk gland.","PeriodicalId":523629,"journal":{"name":"Figshare","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Figshare","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.1021/acs.jproteome.5b00821.s007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Silkworm\nis used as a model organism to analyze two standard complex\ntraits, which are high and low silk yields. To understand the molecular\nmechanisms of silk production, the posterior silk glands aged to the\nthird day of the fifth instar were analyzed from the ZB strain with\nlow silk production and from the control strain Lan10. Using isobaric\ntags for relative and absolute quantification (iTRAQ) quantitative\nshotgun proteomics and RNA-sequencing-based transcriptomics, 139 proteins\nand 630 transcripts were identified as novel in the ZB strain compared\nwith the Lan10 strain, indicating that these results significantly\nexpand the coverage of proteins and transcripts of the posterior silk\nglands in the silkworm. Of the 89 differently changed proteins, 23\nwere increased, and 66 were decreased. Of the 788 transcripts, 779\nwere upregulated, and 9 were downregulated. These results confirm\nthat decreased energy utilization/protein translation and enhanced\nprotein degradation are the key factors in lower silk production.\nMoreover, this study provides novel insight into the molecular changes\nthat may result in lower silk production, namely, a combination of\nimpaired transcription activity, missed protein folding/transport,\nand lowered yields of the main components of fibroin, along with weakened\ngrowth/development of the posterior silk gland.
以家蚕为模型生物,分析了高产和低产丝两种标准复杂性状。为了解产丝的分子机制,对产丝率较低的菌株ZB和对照菌株Lan10进行了5龄至第3 d后丝腺的分析。利用isobaric\ntags for relative and absolute quantification (iTRAQ)定量\nshotgun蛋白质组学和基于rna测序的转录组学,与Lan10菌株相比,ZB菌株鉴定出139个蛋白\nand 630个转录本,这表明这些结果显著扩大了家蚕后丝腺蛋白和转录本的覆盖范围。在89个不同变化的蛋白中,23个蛋白增加,66个蛋白减少。在788个转录本中,779个转录本上调,9个转录本下调。这些结果证实,能量利用/蛋白质翻译的降低和蛋白质降解的增强是导致蚕丝产量下降的关键因素。此外,该研究还对可能导致丝产量下降的分子变化提供了新的见解,即转录活性受损,蛋白质折叠/运输缺失,丝素主要成分产量降低以及后丝腺生长/发育减弱的组合。