Insights into left-right asymmetric development of chicken ovary at the single-cell level.

IF 6.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Genetics and Genomics Pub Date : 2024-11-01 Epub Date: 2024-08-13 DOI:10.1016/j.jgg.2024.08.002
Tao Wang, Dong Leng, Zhongkun Cai, Binlong Chen, Jing Li, Hua Kui, Diyan Li, Zhuanjian Li
{"title":"Insights into left-right asymmetric development of chicken ovary at the single-cell level.","authors":"Tao Wang, Dong Leng, Zhongkun Cai, Binlong Chen, Jing Li, Hua Kui, Diyan Li, Zhuanjian Li","doi":"10.1016/j.jgg.2024.08.002","DOIUrl":null,"url":null,"abstract":"<p><p>Avian ovaries develop asymmetrically apart from prey birds, with only the left ovary growing more towards functional organ. Here, we analyze over 135,000 cells from chick's left and right ovaries at six distinct embryonic developmental stages utilizing single-cell transcriptome sequencing. We delineate gene expression patterns across 15 cell types within these embryo ovaries, revealing side-specific development. The left ovaries exhibit cortex cells, zygotene germ cells, and transcriptional changes unique to the left side. Differential gene expression analysis further identifies specific markers and pathways active in these cell types, highlighting the asymmetry in ovarian development. A fine-scale analysis of the germ cell meiotic transcriptome reveals seven distinct clusters with gene expression patterns specific to various meiotic stages. The study also identifies signaling pathways and intercellular communications, particularly between pre-granulosa and germ cells. Spatial transcriptome analysis shows the asymmetry, demonstrating cortex cells exclusively in the left ovary, modulating neighboring cell types through putative secreted signaling molecules. Overall, this single-cell analysis provides insights into the molecular mechanisms of the asymmetric development of avian ovaries, particularly the significant role of cortex cells in the left ovary.</p>","PeriodicalId":54825,"journal":{"name":"Journal of Genetics and Genomics","volume":" ","pages":"1265-1277"},"PeriodicalIF":6.6000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Genetics and Genomics","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jgg.2024.08.002","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/13 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Avian ovaries develop asymmetrically apart from prey birds, with only the left ovary growing more towards functional organ. Here, we analyze over 135,000 cells from chick's left and right ovaries at six distinct embryonic developmental stages utilizing single-cell transcriptome sequencing. We delineate gene expression patterns across 15 cell types within these embryo ovaries, revealing side-specific development. The left ovaries exhibit cortex cells, zygotene germ cells, and transcriptional changes unique to the left side. Differential gene expression analysis further identifies specific markers and pathways active in these cell types, highlighting the asymmetry in ovarian development. A fine-scale analysis of the germ cell meiotic transcriptome reveals seven distinct clusters with gene expression patterns specific to various meiotic stages. The study also identifies signaling pathways and intercellular communications, particularly between pre-granulosa and germ cells. Spatial transcriptome analysis shows the asymmetry, demonstrating cortex cells exclusively in the left ovary, modulating neighboring cell types through putative secreted signaling molecules. Overall, this single-cell analysis provides insights into the molecular mechanisms of the asymmetric development of avian ovaries, particularly the significant role of cortex cells in the left ovary.

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
在单细胞水平上揭示鸡卵巢左右不对称的发育过程
除猎禽外,鸟类的卵巢发育并不对称,只有左侧卵巢的发育更趋向于功能性器官。在这里,我们利用单细胞转录组测序技术分析了小鸡左右卵巢在六个不同胚胎发育阶段的 135,000 多个细胞。我们描绘了这些胚胎卵巢中 15 种细胞类型的基因表达模式,揭示了卵巢发育的两侧特异性。左侧卵巢表现出皮质细胞、胚胎生殖细胞以及左侧特有的转录变化。差异基因表达分析进一步确定了这些细胞类型中活跃的特定标记和通路,凸显了卵巢发育的不对称性。对生殖细胞减数分裂转录组的精细分析表明,不同减数分裂阶段有七个不同的基因表达模式群。研究还确定了信号通路和细胞间通信,尤其是前颗粒细胞和生殖细胞之间的通信。空间转录组分析显示了不对称性,表明皮质细胞只存在于左侧卵巢,通过推测的分泌信号分子调节邻近的细胞类型。总之,这项单细胞分析深入揭示了鸟类卵巢不对称发育的分子机制,尤其是皮层细胞在左侧卵巢中的重要作用。
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
Journal of Genetics and Genomics
Journal of Genetics and Genomics 生物-生化与分子生物学
CiteScore
8.20
自引率
3.40%
发文量
4756
审稿时长
14 days
期刊介绍: The Journal of Genetics and Genomics (JGG, formerly known as Acta Genetica Sinica ) is an international journal publishing peer-reviewed articles of novel and significant discoveries in the fields of genetics and genomics. Topics of particular interest include but are not limited to molecular genetics, developmental genetics, cytogenetics, epigenetics, medical genetics, population and evolutionary genetics, genomics and functional genomics as well as bioinformatics and computational biology.
期刊最新文献
Deciphering the influence of gut and oral microbiomes on menopause for healthy aging. KanCell: dissecting cellular heterogeneity in biological tissues through integrated single-cell and spatial transcriptomics. Genomic insights into the genetic diversity, lateral gaits and high-altitude adaptation of Chakouyi (CKY) horses. Integrated analysis and systematic characterization of the regulatory network for human germline development. Znf706 regulates germ plasm assembly and primordial germ cell development in zebrafish.
×
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