Female Germline Cysts in Animals: Evolution and Function.

Q4 Biochemistry, Genetics and Molecular Biology Results and Problems in Cell Differentiation Pub Date : 2024-01-01 DOI:10.1007/978-3-031-37936-9_2
John L Brubacher
{"title":"Female Germline Cysts in Animals: Evolution and Function.","authors":"John L Brubacher","doi":"10.1007/978-3-031-37936-9_2","DOIUrl":null,"url":null,"abstract":"<p><p>Germline cysts are syncytia formed by incomplete cytokinesis of mitotic germline precursors (cystoblasts) in which the cystocytes are interconnected by cytoplasmic bridges, permitting the sharing of molecules and organelles. Among animals, such cysts are a nearly universal feature of spermatogenesis and are also often involved in oogenesis. Recent, elegant studies have demonstrated remarkable similarities in the oogenic cysts of mammals and insects, leading to proposals of widespread conservation of these features among animals. Unfortunately, such claims obscure the well-described diversity of female germline cysts in animals and ignore major taxa in which female germline cysts appear to be absent. In this review, I explore the phylogenetic patterns of oogenic cysts in the animal kingdom, with a focus on the hexapods as an informative example of a clade in which such cysts have been lost, regained, and modified in various ways. My aim is to build on the fascinating insights of recent comparative studies, by calling for a more nuanced view of evolutionary conservation. Female germline cysts in the Metazoa are an example of a phenomenon that-though essential for the continuance of many, diverse animal lineages-nevertheless exhibits intriguing patterns of evolutionary innovation, loss, and convergence.</p>","PeriodicalId":39320,"journal":{"name":"Results and Problems in Cell Differentiation","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results and Problems in Cell Differentiation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-3-031-37936-9_2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

Germline cysts are syncytia formed by incomplete cytokinesis of mitotic germline precursors (cystoblasts) in which the cystocytes are interconnected by cytoplasmic bridges, permitting the sharing of molecules and organelles. Among animals, such cysts are a nearly universal feature of spermatogenesis and are also often involved in oogenesis. Recent, elegant studies have demonstrated remarkable similarities in the oogenic cysts of mammals and insects, leading to proposals of widespread conservation of these features among animals. Unfortunately, such claims obscure the well-described diversity of female germline cysts in animals and ignore major taxa in which female germline cysts appear to be absent. In this review, I explore the phylogenetic patterns of oogenic cysts in the animal kingdom, with a focus on the hexapods as an informative example of a clade in which such cysts have been lost, regained, and modified in various ways. My aim is to build on the fascinating insights of recent comparative studies, by calling for a more nuanced view of evolutionary conservation. Female germline cysts in the Metazoa are an example of a phenomenon that-though essential for the continuance of many, diverse animal lineages-nevertheless exhibits intriguing patterns of evolutionary innovation, loss, and convergence.

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
动物雌性生殖系囊肿:进化和功能。
生殖系包囊是由有丝分裂的生殖系前体(囊母细胞)的不完全胞质分裂形成的合胞体,其中囊细胞通过细胞质桥相互连接,允许共享分子和细胞器。在动物中,这种囊肿几乎是精子发生的普遍特征,也经常涉及卵子发生。最近,一些优雅的研究已经证明了哺乳动物和昆虫的卵囊有显著的相似之处,从而提出了在动物中广泛保护这些特征的建议。不幸的是,这种说法模糊了动物中雌性生殖系囊肿的多样性,并忽略了雌性生殖系囊肿似乎不存在的主要分类群。在这篇综述中,我探索了动物王国中卵源性囊肿的系统发育模式,并将重点放在六足动物身上,作为一个信息丰富的例子,在这个进化分支中,这种囊肿以各种方式丢失、恢复和修改。我的目的是建立在最近比较研究的迷人见解的基础上,呼吁对进化守恒有更细致入微的看法。后生动物的雌性生殖系囊肿是一种现象的例子,尽管这种现象对许多不同的动物谱系的延续至关重要,但它仍然表现出有趣的进化创新、丧失和趋同模式。
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
Results and Problems in Cell Differentiation
Results and Problems in Cell Differentiation Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
1.90
自引率
0.00%
发文量
21
期刊介绍: Results and Problems in Cell Differentiation is an up-to-date book series that presents and explores selected questions of cell and developmental biology. Each volume focuses on a single, well-defined topic. Reviews address basic questions and phenomena, but also provide concise information on the most recent advances. Together, the volumes provide a valuable overview of this exciting and dynamically expanding field.
期刊最新文献
Early Syncytialization of the Ovine Placenta Revisited. HIV-1 Induced Cell-to-Cell Fusion or Syncytium Formation. Mathematical Modeling of Virus-Mediated Syncytia Formation: Past Successes and Future Directions. Muscle Progenitor Cell Fusion in the Maintenance of Skeletal Muscle. Osteoclasts at Bone Remodeling: Order from Order.
×
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