A novel role for ATP2B in ascidians: Ascidian-specific mutations in ATP2B contribute to sperm chemotaxis

IF 1.7 3区 生物学 Q3 DEVELOPMENTAL BIOLOGY Journal of experimental zoology. Part B, Molecular and developmental evolution Pub Date : 2022-04-25 DOI:10.1002/jez.b.23133
Jumpei Ikenaga, Satoe Aratake, Kaoru Yoshida, Manabu Yoshida
{"title":"A novel role for ATP2B in ascidians: Ascidian-specific mutations in ATP2B contribute to sperm chemotaxis","authors":"Jumpei Ikenaga,&nbsp;Satoe Aratake,&nbsp;Kaoru Yoshida,&nbsp;Manabu Yoshida","doi":"10.1002/jez.b.23133","DOIUrl":null,"url":null,"abstract":"<p>Sperm chemotaxis, in which sperms are attracted to conspecific eggs via species-specific attractants, plays an important role in fertilization. This phenomenon has been observed in various animals and species-specific sperm attractants have been reported in some species. However, the mechanisms involved in the reception and recognition of the species-specific attractant by the sperms is poorly studied. Previously, we found that the plasma membrane-type Ca<sup>2+</sup>/ATPase (PMCA) is the receptor for the sperm-activating and -attracting factor (SAAF) in the ascidian <i>Ciona intestinalis</i>. To determine the role of PMCA in species-specific sperm chemotaxis, we identified the amino acid sequences of PMCAs derived from six Phlebobranchia species. The testis-specific splice variant of PMCA was found to be present in all the species investigated and the ascidian-specific sequence was detected near the 3′-terminus. Moreover, dN/dS analysis revealed that the extracellular loops 1, 2, and 4 in ascidian PMCA underwent a positive selection. These findings suggest that PMCA recognizes the species-specific structure of SAAF at the extracellular loops 1, 2, and 4, and its testis-specific C-terminal region is involved in the activation and chemotaxis of ascidian sperms.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"338 7","pages":"430-437"},"PeriodicalIF":1.7000,"publicationDate":"2022-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of experimental zoology. Part B, Molecular and developmental evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jez.b.23133","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Sperm chemotaxis, in which sperms are attracted to conspecific eggs via species-specific attractants, plays an important role in fertilization. This phenomenon has been observed in various animals and species-specific sperm attractants have been reported in some species. However, the mechanisms involved in the reception and recognition of the species-specific attractant by the sperms is poorly studied. Previously, we found that the plasma membrane-type Ca2+/ATPase (PMCA) is the receptor for the sperm-activating and -attracting factor (SAAF) in the ascidian Ciona intestinalis. To determine the role of PMCA in species-specific sperm chemotaxis, we identified the amino acid sequences of PMCAs derived from six Phlebobranchia species. The testis-specific splice variant of PMCA was found to be present in all the species investigated and the ascidian-specific sequence was detected near the 3′-terminus. Moreover, dN/dS analysis revealed that the extracellular loops 1, 2, and 4 in ascidian PMCA underwent a positive selection. These findings suggest that PMCA recognizes the species-specific structure of SAAF at the extracellular loops 1, 2, and 4, and its testis-specific C-terminal region is involved in the activation and chemotaxis of ascidian sperms.

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
ATP2B在海鞘中的新作用:ATP2B在海鞘中的特异性突变有助于精子趋化
精子趋化作用是指精子通过物种特异性引诱剂被同种卵子吸引,在受精过程中起着重要作用。这种现象已经在许多动物中观察到,并且在一些物种中报道了特定物种的精子引诱剂。然而,精子接受和识别物种特异性引诱剂的机制研究甚少。在此之前,我们发现质膜型Ca2+/ atp酶(PMCA)是海鞘精子激活和吸引因子(SAAF)的受体。为了确定PMCA在物种特异性精子趋化性中的作用,我们鉴定了来自六种细鳃鱼的PMCA的氨基酸序列。PMCA的睾丸特异性剪接变体在所有被调查的物种中都存在,并且在3 '端附近检测到海鞘特异性序列。此外,dN/dS分析显示,海鞘PMCA细胞外环1、2和4发生了正选择。这些发现表明PMCA在细胞外环1、2和4处识别SAAF的物种特异性结构,其睾丸特异性c端区域参与了海鞘精子的激活和趋化。
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
CiteScore
4.80
自引率
9.10%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Developmental Evolution is a branch of evolutionary biology that integrates evidence and concepts from developmental biology, phylogenetics, comparative morphology, evolutionary genetics and increasingly also genomics, systems biology as well as synthetic biology to gain an understanding of the structure and evolution of organisms. The Journal of Experimental Zoology -B: Molecular and Developmental Evolution provides a forum where these fields are invited to bring together their insights to further a synthetic understanding of evolution from the molecular through the organismic level. Contributions from all these branches of science are welcome to JEZB. We particularly encourage submissions that apply the tools of genomics, as well as systems and synthetic biology to developmental evolution. At this time the impact of these emerging fields on developmental evolution has not been explored to its fullest extent and for this reason we are eager to foster the relationship of systems and synthetic biology with devo evo.
期刊最新文献
Gene Expression During Scale Development in Pachyrhynchus Weevils Escaping Constraints to Innovate: Maternal Neofunctionalization in a HoxB4 Duplicate Reduced Dietary Protein Induces Changes in the Dental Proteome On the Heterochrony and Evolution of Oral Structures in Phyllopharyngean Ciliates (Protista: Ciliophora) Issue Information
×
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:604180095
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