Comparative transcriptome analysis reveals molecular mechanisms of the effects of light intensity and photoperiod on ovarian development in Procambarus clarkii (Girard, 1852)

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
{"title":"Comparative transcriptome analysis reveals molecular mechanisms of the effects of light intensity and photoperiod on ovarian development in Procambarus clarkii (Girard, 1852)","authors":"","doi":"10.1016/j.cbd.2024.101329","DOIUrl":null,"url":null,"abstract":"<div><p><em>Procambarus clarkii</em> (Girard, 1852) has important economic value in China and internationally. In this research, the comparative transcriptome analysis was used to reveal molecular mechanisms of influences of photoperiod and light intensity on ovarian development in <em>P. clarkii</em> for the first time. Some genes (such as <em>laminin</em>, <em>collagen</em>, <em>integrin beta</em>, <em>catenin</em>) and pathways (including TGF-beta signaling pathway, focal adhesion, ECM–receptor interaction) associated with ovarian development and oocyte maturation were significantly upregulated. Some genes related to circadian clock (such as <em>CLK</em>, <em>PER</em>) were identified in this research. The results indicated that when light intensity or photoperiod increased, <em>P. clarkii</em> could up-regulate the expression levels of the <em>laminin</em> and <em>collagen</em>, thereby synthesizing related proteins, promoting meiosis of the oocytes, thus increasing the number of oocytes in the ovary. At the same time, <em>P. clarkii</em> could up-regulate the expression levels of <em>integrin beta</em>, <em>integrin alpha 6</em>, and <em>diacylglycerol</em> to synthesize related proteins, thereby promoting the formation of proteins and fats such as triglycerides, these proteins and fats can provide material basis for maturation and development of oocytes, resulting in oocyte maturation and ovarian development. <em>P. clarkii</em> could synthesize related proteins by upregulating expression levels of genes (such as <em>catenin</em>), these proteins or hormones can adhere to other actins (such as integrins), thereby stabilizing the morphology of the oocytes and ensuring normal development. Meantime, the increase in light intensity or photoperiod could cause release GSH and VTG, resulting in oocytes development and maturation. The data in this research can reveal molecular mechanisms of impacts of photoperiod and light intensity on oocyte maturation and ovarian development in <em>P. clarkii</em>, can offer crucial genomic data for studying developmental mechanisms of ovary and oocyte in crustacean.</p></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2024-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X24001424","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Procambarus clarkii (Girard, 1852) has important economic value in China and internationally. In this research, the comparative transcriptome analysis was used to reveal molecular mechanisms of influences of photoperiod and light intensity on ovarian development in P. clarkii for the first time. Some genes (such as laminin, collagen, integrin beta, catenin) and pathways (including TGF-beta signaling pathway, focal adhesion, ECM–receptor interaction) associated with ovarian development and oocyte maturation were significantly upregulated. Some genes related to circadian clock (such as CLK, PER) were identified in this research. The results indicated that when light intensity or photoperiod increased, P. clarkii could up-regulate the expression levels of the laminin and collagen, thereby synthesizing related proteins, promoting meiosis of the oocytes, thus increasing the number of oocytes in the ovary. At the same time, P. clarkii could up-regulate the expression levels of integrin beta, integrin alpha 6, and diacylglycerol to synthesize related proteins, thereby promoting the formation of proteins and fats such as triglycerides, these proteins and fats can provide material basis for maturation and development of oocytes, resulting in oocyte maturation and ovarian development. P. clarkii could synthesize related proteins by upregulating expression levels of genes (such as catenin), these proteins or hormones can adhere to other actins (such as integrins), thereby stabilizing the morphology of the oocytes and ensuring normal development. Meantime, the increase in light intensity or photoperiod could cause release GSH and VTG, resulting in oocytes development and maturation. The data in this research can reveal molecular mechanisms of impacts of photoperiod and light intensity on oocyte maturation and ovarian development in P. clarkii, can offer crucial genomic data for studying developmental mechanisms of ovary and oocyte in crustacean.

Abstract Image

比较转录组分析揭示光照强度和光周期对克氏原鲤(Procambarus clarkii)(Girard,1852)卵巢发育影响的分子机制
黄颡鱼(Procambarus clarkii)(Girard,1852)在中国和国际上都具有重要的经济价值。本研究首次利用比较转录组分析揭示了光周期和光照强度对黄颡鱼卵巢发育的影响分子机制。与卵巢发育和卵母细胞成熟相关的一些基因(如层粘连蛋白、胶原蛋白、整合素β、catenin)和通路(包括TGF-beta信号通路、局灶粘附、ECM-受体相互作用)被显著上调。本研究还发现了一些与昼夜节律相关的基因(如 CLK、PER)。结果表明,当光照强度或光周期增加时,P. clarkii 能上调层粘连蛋白和胶原蛋白的表达水平,从而合成相关蛋白,促进卵母细胞的减数分裂,从而增加卵巢中卵母细胞的数量。同时,P. clarkii 能上调整合素 beta、整合素 alpha 6 和二酰甘油的表达水平,合成相关蛋白质,从而促进甘油三酯等蛋白质和脂肪的形成,这些蛋白质和脂肪能为卵母细胞的成熟和发育提供物质基础,导致卵母细胞成熟和卵巢发育。克氏原藻类可以通过上调基因(如 catenin)的表达水平来合成相关蛋白质,这些蛋白质或激素可以粘附在其他肌动蛋白(如整合素)上,从而稳定卵母细胞的形态,保证卵母细胞的正常发育。同时,光照强度或光周期的增加可导致 GSH 和 VTG 的释放,从而促进卵母细胞的发育和成熟。该研究数据揭示了光周期和光照强度对克氏原螯虾卵母细胞成熟和卵巢发育的分子机制,为研究甲壳类动物卵巢和卵母细胞的发育机制提供了重要的基因组数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信