Transcriptomic and metabolomic analyses reveal sex-related differences in the gonads of Pinctada fucata martensii

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-08-02 DOI:10.1016/j.cbd.2024.101304
Jiaying Fang , Chuangye Yang , Yongshan Liao , Qingheng Wang , Yuewen Deng
{"title":"Transcriptomic and metabolomic analyses reveal sex-related differences in the gonads of Pinctada fucata martensii","authors":"Jiaying Fang ,&nbsp;Chuangye Yang ,&nbsp;Yongshan Liao ,&nbsp;Qingheng Wang ,&nbsp;Yuewen Deng","doi":"10.1016/j.cbd.2024.101304","DOIUrl":null,"url":null,"abstract":"<div><p><em>Pinctada fucata martensii</em> is an economically important bivalve mollusk, as this species makes a major contribution to seawater pearl production. Pearl production efficiency varies between the sexes of <em>P. f. martensii</em>, but many aspects of the molecular mechanisms underlying sex determination and sex differentiation in <em>P. f. martensii</em> remain unclear. Here, transcriptomic and metabonomic analyses were conducted to identify the major genes and metabolic changes associated with sex determination and gametogenesis. We identified a total of 3426 differentially expressed genes (DEGs) between females and males. These included <em>Fem-1c</em> and <em>Foxl2</em>, which are involved in sex determination and sex differentiation, and <em>SOHLH2</em>, <em>Nanos1</em> and <em>TSSK4</em>, which are involved in gametogenesis. We also identified a total of 5231 significant differential metabolites (SDMs) between females and males. These DEGs were enriched in 47 metabolic pathways, including “ABC transporters,” “purine metabolism,” and “glycerophospholipid metabolism.” Our findings provide new insights into the molecular mechanisms underlying sex determination, sex differentiation, and gametogenesis and will aid future studies of <em>P. f. martensii</em>.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X24001175","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Pinctada fucata martensii is an economically important bivalve mollusk, as this species makes a major contribution to seawater pearl production. Pearl production efficiency varies between the sexes of P. f. martensii, but many aspects of the molecular mechanisms underlying sex determination and sex differentiation in P. f. martensii remain unclear. Here, transcriptomic and metabonomic analyses were conducted to identify the major genes and metabolic changes associated with sex determination and gametogenesis. We identified a total of 3426 differentially expressed genes (DEGs) between females and males. These included Fem-1c and Foxl2, which are involved in sex determination and sex differentiation, and SOHLH2, Nanos1 and TSSK4, which are involved in gametogenesis. We also identified a total of 5231 significant differential metabolites (SDMs) between females and males. These DEGs were enriched in 47 metabolic pathways, including “ABC transporters,” “purine metabolism,” and “glycerophospholipid metabolism.” Our findings provide new insights into the molecular mechanisms underlying sex determination, sex differentiation, and gametogenesis and will aid future studies of P. f. martensii.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
转录组和代谢组分析揭示了 Pinctada fucata martensii 性腺中与性别有关的差异。
Pinctada fucata martensii 是一种具有重要经济价值的双壳软体动物,因为该物种对海水珍珠生产做出了重大贡献。P. f. martensii的珍珠生产效率因性别而异,但P. f. martensii性别决定和性别分化的分子机制的许多方面仍不清楚。在此,我们进行了转录组学和代谢组学分析,以确定与性别决定和配子发生相关的主要基因和代谢变化。我们共发现了 3426 个雌性和雄性之间的差异表达基因(DEGs)。其中包括参与性别决定和性别分化的Fem-1c和Foxl2,以及参与配子发生的SOHLH2、Nanos1和TSSK4。我们还发现了 5231 个雌性和雄性之间的显著差异代谢物(SDMs)。这些DEGs富集在47个代谢途径中,包括 "ABC转运体"、"嘌呤代谢 "和 "甘油磷脂代谢"。我们的研究结果为性别决定、性别分化和配子发生的分子机制提供了新的见解,并将有助于今后对貂蝉的研究。
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 去求助
来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊最新文献
A Systematic Review of Sleep Disturbance in Idiopathic Intracranial Hypertension. Advancing Patient Education in Idiopathic Intracranial Hypertension: The Promise of Large Language Models. Anti-Myelin-Associated Glycoprotein Neuropathy: Recent Developments. Approach to Managing the Initial Presentation of Multiple Sclerosis: A Worldwide Practice Survey. Association Between LACE+ Index Risk Category and 90-Day Mortality After Stroke.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1