Morpho-histological and Transcriptome Analysis Reveal the Unreduced Sperm Formation Mechanism in cdk1-Depletion Zebrafish

IF 2.6 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yunbang Zhang, Rongyun Li, Hui Li, Yuwei Huang, Yihui Mei, Yuxuan Zheng, Yankun Guo, Zihao Zhou, Zhonglin Yong, Ying Zhao, Wenjing Dong, Jian Gao, Xiaojuan Cao
{"title":"Morpho-histological and Transcriptome Analysis Reveal the Unreduced Sperm Formation Mechanism in cdk1-Depletion Zebrafish","authors":"Yunbang Zhang,&nbsp;Rongyun Li,&nbsp;Hui Li,&nbsp;Yuwei Huang,&nbsp;Yihui Mei,&nbsp;Yuxuan Zheng,&nbsp;Yankun Guo,&nbsp;Zihao Zhou,&nbsp;Zhonglin Yong,&nbsp;Ying Zhao,&nbsp;Wenjing Dong,&nbsp;Jian Gao,&nbsp;Xiaojuan Cao","doi":"10.1007/s10126-024-10366-0","DOIUrl":null,"url":null,"abstract":"<div><p>Cyclin-dependent kinases (Cdks) are major molecules related to cell cycle regulation. Polyploidy can be caused by the production of unreduced gametes, which is often related to the abnormal cell cycle of germ cells. Here, we successfully constructed a <i>cdk1</i> mutation line (<i>cdk1</i><sup>+<i>/−</i></sup>) in zebrafish, a commonly used model organism. It showed that <i>cdk1</i> depletion resulted in the generation of both polyploid and aneuploid embryos of WT♀ × <i>cdk1</i><sup>+<i>/−</i></sup><i>♂</i> zebrafish. In addition to normal sperms (1N), the depletion of <i>cdk1</i> in zebrafish also led to the production of some large-head 2N sperms and higher ploidy sperms. Results of bivalent analysis of testis and ultrastructure analysis of spermatogonia suggested that the production of these large-head sperms was due to spermatogonia chromosome doubling in <i>cdk1</i><sup>+<i>/−</i></sup> zebrafish. Transcriptome analysis revealed aberrant expressions of some cell cycle and DNA replication-related genes in the early testis of <i>cdk1</i><sup>+<i>/−</i></sup> zebrafish relative to WT zebrafish. Through STRING correlation analysis, we further proved that <i>cdk1</i> depletion affected the mitosis process and endoduplication initiation of spermatogonia by regulating expressions of some proteins related to cell cycle (i.e., Espl1 and Pp1) and DNA replication (i.e., Orc1 and Rnaseh2b), thereby leading to the formation of unreduced sperms. This study provides important information on revealing the molecular mechanisms of unreduced gamete formation caused by <i>cdk1</i> mutation. Meanwhile, it also provides an important reference for the creation of fish polyploid germplasm.</p></div>","PeriodicalId":690,"journal":{"name":"Marine Biotechnology","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2024-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Marine Biotechnology","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s10126-024-10366-0","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Cyclin-dependent kinases (Cdks) are major molecules related to cell cycle regulation. Polyploidy can be caused by the production of unreduced gametes, which is often related to the abnormal cell cycle of germ cells. Here, we successfully constructed a cdk1 mutation line (cdk1+/−) in zebrafish, a commonly used model organism. It showed that cdk1 depletion resulted in the generation of both polyploid and aneuploid embryos of WT♀ × cdk1+/− zebrafish. In addition to normal sperms (1N), the depletion of cdk1 in zebrafish also led to the production of some large-head 2N sperms and higher ploidy sperms. Results of bivalent analysis of testis and ultrastructure analysis of spermatogonia suggested that the production of these large-head sperms was due to spermatogonia chromosome doubling in cdk1+/− zebrafish. Transcriptome analysis revealed aberrant expressions of some cell cycle and DNA replication-related genes in the early testis of cdk1+/− zebrafish relative to WT zebrafish. Through STRING correlation analysis, we further proved that cdk1 depletion affected the mitosis process and endoduplication initiation of spermatogonia by regulating expressions of some proteins related to cell cycle (i.e., Espl1 and Pp1) and DNA replication (i.e., Orc1 and Rnaseh2b), thereby leading to the formation of unreduced sperms. This study provides important information on revealing the molecular mechanisms of unreduced gamete formation caused by cdk1 mutation. Meanwhile, it also provides an important reference for the creation of fish polyploid germplasm.

Abstract Image

形态组学和转录组分析揭示 cdk1 缺失斑马鱼的精子形成机制
细胞周期蛋白依赖性激酶(Cdks)是与细胞周期调控有关的主要分子。多倍体可由未还原配子的产生引起,而未还原配子的产生往往与生殖细胞的细胞周期异常有关。在这里,我们成功地在斑马鱼(一种常用的模式生物)中构建了一个 cdk1 突变系(cdk1+/-)。结果表明,cdk1缺失会导致WT♀ × cdk1+/-♂斑马鱼产生多倍体和非整倍体胚胎。除了正常精子(1N)外,斑马鱼中 cdk1 的耗竭还导致产生一些大头 2N 精子和更高倍性的精子。睾丸二价分析和精原细胞超微结构分析结果表明,这些大头精子的产生是由于 cdk1+/- 斑马鱼精原细胞染色体加倍所致。转录组分析显示,相对于WT斑马鱼,cdk1+/-斑马鱼早期睾丸中一些细胞周期和DNA复制相关基因的表达异常。通过STRING相关分析,我们进一步证实了cdk1缺失通过调节一些与细胞周期(即Espl1和Pp1)和DNA复制(即Orc1和Rnaseh2b)相关的蛋白的表达,影响了精原细胞的有丝分裂过程和内复制的启动,从而导致未还原精子的形成。这项研究为揭示 cdk1 基因突变导致配子形成不还原的分子机制提供了重要信息。同时,也为鱼类多倍体种质的培育提供了重要参考。
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
Marine Biotechnology
Marine Biotechnology 工程技术-海洋与淡水生物学
CiteScore
4.80
自引率
3.30%
发文量
95
审稿时长
2 months
期刊介绍: Marine Biotechnology welcomes high-quality research papers presenting novel data on the biotechnology of aquatic organisms. The journal publishes high quality papers in the areas of molecular biology, genomics, proteomics, cell biology, and biochemistry, and particularly encourages submissions of papers related to genome biology such as linkage mapping, large-scale gene discoveries, QTL analysis, physical mapping, and comparative and functional genome analysis. Papers on technological development and marine natural products should demonstrate innovation and novel applications.
×
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