Steroid hormone-deprived sex reversal in cyp11a1 mutant XX tilapia experiences an ovary-like stage at molecular level

IF 5.2 1区 生物学 Q1 BIOLOGY Communications Biology Pub Date : 2024-09-16 DOI:10.1038/s42003-024-06853-8
Hesheng Xiao, Leihui Wang, Shuo Yan, He Ma, Zhen Xu, Feilong Wang, Jingrong Wang, Wenjing Tao, Deshou Wang
{"title":"Steroid hormone-deprived sex reversal in cyp11a1 mutant XX tilapia experiences an ovary-like stage at molecular level","authors":"Hesheng Xiao, Leihui Wang, Shuo Yan, He Ma, Zhen Xu, Feilong Wang, Jingrong Wang, Wenjing Tao, Deshou Wang","doi":"10.1038/s42003-024-06853-8","DOIUrl":null,"url":null,"abstract":"Fish sex is largely influenced by steroid hormones, especially sex hormones. Here, we established a steroid hormone-free genetic model by mutation of cyp11a1 in Nile tilapia, which was confirmed by EIA assay. Gonadal phenotype and transcriptome analyses showed that the XX mutants displayed sex reversal from female to male but with defective spermatogenesis. Despite the sex reversal, the aromatase encoding gene cyp19a1a was continuously expressed in the gonads of the XX mutants, which might be caused by androgen deficiency. Whole-mount fluorescence in situ hybridization and transcriptome analysis showed that the gonads of the XX mutants firstly developed towards ovary but shifted to testis between 10 to 15 days after hatching. Detailed expression analysis of key sex differentiation pathway genes foxl3 and dmrt1 combined with apoptosis analysis revealed transdifferentiation of germ cells from female to male during sex reversal. Rescue experiments showed that both P5 and E2 treatment rescued the sex reversal of cyp11a1 mutant XX fish. Overall, our results revealed a transient ovary-like stage and transdifferentiation of germ cells from female to male in the early gonads of the steroid hormone-deprived cyp11a1 mutant XX fish. Revealing of a transient ovary-like stage and transdifferentiation of germ cells from female to male in the early gonads of the XX fish after steroid hormone-deprivation.","PeriodicalId":10552,"journal":{"name":"Communications Biology","volume":null,"pages":null},"PeriodicalIF":5.2000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s42003-024-06853-8.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications Biology","FirstCategoryId":"99","ListUrlMain":"https://www.nature.com/articles/s42003-024-06853-8","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Fish sex is largely influenced by steroid hormones, especially sex hormones. Here, we established a steroid hormone-free genetic model by mutation of cyp11a1 in Nile tilapia, which was confirmed by EIA assay. Gonadal phenotype and transcriptome analyses showed that the XX mutants displayed sex reversal from female to male but with defective spermatogenesis. Despite the sex reversal, the aromatase encoding gene cyp19a1a was continuously expressed in the gonads of the XX mutants, which might be caused by androgen deficiency. Whole-mount fluorescence in situ hybridization and transcriptome analysis showed that the gonads of the XX mutants firstly developed towards ovary but shifted to testis between 10 to 15 days after hatching. Detailed expression analysis of key sex differentiation pathway genes foxl3 and dmrt1 combined with apoptosis analysis revealed transdifferentiation of germ cells from female to male during sex reversal. Rescue experiments showed that both P5 and E2 treatment rescued the sex reversal of cyp11a1 mutant XX fish. Overall, our results revealed a transient ovary-like stage and transdifferentiation of germ cells from female to male in the early gonads of the steroid hormone-deprived cyp11a1 mutant XX fish. Revealing of a transient ovary-like stage and transdifferentiation of germ cells from female to male in the early gonads of the XX fish after steroid hormone-deprivation.

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
cyp11a1突变体XX罗非鱼的类固醇激素剥夺性逆转在分子水平上经历了卵巢样阶段
鱼类的性别在很大程度上受类固醇激素,尤其是性激素的影响。在这里,我们通过突变尼罗罗非鱼的cyp11a1,建立了一个不含类固醇激素的遗传模型,并通过EIA检测证实了这一点。性腺表型和转录组分析表明,XX突变体表现出从雌性到雄性的性别逆转,但精子发生有缺陷。尽管出现了性别逆转,但芳香化酶编码基因cyp19a1a在XX突变体的性腺中持续表达,这可能是雄激素缺乏所致。整装荧光原位杂交和转录组分析表明,XX突变体的性腺最初向卵巢方向发育,但在孵化后10至15天内转向睾丸。对性别分化途径关键基因 foxl3 和 dmrt1 的详细表达分析以及细胞凋亡分析表明,在性别逆转过程中,生殖细胞从雌性向雄性发生了转分化。拯救实验表明,P5和E2处理都能拯救cyp11a1突变XX鱼的性别逆转。总之,我们的研究结果表明,在类固醇激素缺乏的cyp11a1突变体XX鱼的早期性腺中,出现了短暂的卵巢样阶段和生殖细胞由雌性向雄性的转分化。揭示了类固醇激素剥夺后,XX鱼早期性腺中生殖细胞由雌性向雄性的短暂卵巢样阶段和转分化。
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
Communications Biology
Communications Biology Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
1.70%
发文量
1233
审稿时长
13 weeks
期刊介绍: Communications Biology is an open access journal from Nature Research publishing high-quality research, reviews and commentary in all areas of the biological sciences. Research papers published by the journal represent significant advances bringing new biological insight to a specialized area of research.
期刊最新文献
Iterative crRNA design and a PAM-free strategy enabled an ultra-specific RPA-CRISPR/Cas12a detection platform. Discovery of a family of menaquinone-targeting cyclic lipodepsipeptides for multidrug-resistant Gram-positive pathogens. KLF13 promotes SLE pathogenesis by modifying chromatin accessibility of key proinflammatory cytokine genes. Mutational signature analyses in multi-child families reveal sources of age-related increases in human germline mutations. Sources of variation in the serum metabolome of female participants of the HUNT2 study.
×
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