降低LONP1表达有助于卵母细胞DNA损伤和减数分裂缺陷

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Chuanming Liu, Manlin Xu, Yajie Guan, Lilin Li, Wenwen Liu, Bichun Guo, Xiaoqiang Sheng, Yang Zhang, Jidong Zhou, Xin Zhen, Guijun Yan, Haixiang Sun, Lijun Ding
{"title":"降低LONP1表达有助于卵母细胞DNA损伤和减数分裂缺陷","authors":"Chuanming Liu,&nbsp;Manlin Xu,&nbsp;Yajie Guan,&nbsp;Lilin Li,&nbsp;Wenwen Liu,&nbsp;Bichun Guo,&nbsp;Xiaoqiang Sheng,&nbsp;Yang Zhang,&nbsp;Jidong Zhou,&nbsp;Xin Zhen,&nbsp;Guijun Yan,&nbsp;Haixiang Sun,&nbsp;Lijun Ding","doi":"10.1002/mrd.23694","DOIUrl":null,"url":null,"abstract":"<p>Meiotic defects in oocytes are the primary reason for decreased female fertility with advanced maternal age. In this study, we revealed that decreased expression of ATP-dependent Lon peptidase 1 (LONP1) in aged oocytes and oocyte-specific depletion of <i>LONP1</i> disrupt oocyte meiotic progression accompanying with mitochondrial dysfunction. In addition, LONP1 downregulation increased oocyte DNA damage. Moreover, we demonstrated that splicing factor proline and glutamine rich directly interacts with LONP1 and mediate the effect of LONP1 depletion on meiotic progression in oocytes. In summary, our data suggest that decreased expression of LONP1 is involved in advanced maternal age-related meiosis defects and that LONP1 represents a new therapeutic target to improve aged oocyte quality.</p>","PeriodicalId":18856,"journal":{"name":"Molecular Reproduction and Development","volume":"90 6","pages":"358-368"},"PeriodicalIF":2.7000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Decreased LONP1 expression contributes to DNA damage and meiotic defects in oocytes\",\"authors\":\"Chuanming Liu,&nbsp;Manlin Xu,&nbsp;Yajie Guan,&nbsp;Lilin Li,&nbsp;Wenwen Liu,&nbsp;Bichun Guo,&nbsp;Xiaoqiang Sheng,&nbsp;Yang Zhang,&nbsp;Jidong Zhou,&nbsp;Xin Zhen,&nbsp;Guijun Yan,&nbsp;Haixiang Sun,&nbsp;Lijun Ding\",\"doi\":\"10.1002/mrd.23694\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Meiotic defects in oocytes are the primary reason for decreased female fertility with advanced maternal age. In this study, we revealed that decreased expression of ATP-dependent Lon peptidase 1 (LONP1) in aged oocytes and oocyte-specific depletion of <i>LONP1</i> disrupt oocyte meiotic progression accompanying with mitochondrial dysfunction. In addition, LONP1 downregulation increased oocyte DNA damage. Moreover, we demonstrated that splicing factor proline and glutamine rich directly interacts with LONP1 and mediate the effect of LONP1 depletion on meiotic progression in oocytes. In summary, our data suggest that decreased expression of LONP1 is involved in advanced maternal age-related meiosis defects and that LONP1 represents a new therapeutic target to improve aged oocyte quality.</p>\",\"PeriodicalId\":18856,\"journal\":{\"name\":\"Molecular Reproduction and Development\",\"volume\":\"90 6\",\"pages\":\"358-368\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2023-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Reproduction and Development\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/mrd.23694\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Reproduction and Development","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mrd.23694","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

卵母细胞的减数分裂缺陷是高龄产妇生育能力下降的主要原因。在这项研究中,我们发现,衰老卵母细胞中ATP依赖性Lon肽酶1(LONP1)的表达减少和卵母细胞特异性LONP1的缺失破坏了卵母细胞减数分裂进程,并伴有线粒体功能障碍。此外,LONP1下调增加了卵母细胞DNA损伤。此外,我们证明了富含脯氨酸和谷氨酰胺的剪接因子直接与LONP1相互作用,并介导LONP1缺失对卵母细胞减数分裂进程的影响。总之,我们的数据表明,LONP1表达的减少与晚期母体年龄相关的减数分裂缺陷有关,并且LONP1代表了改善衰老卵母细胞质量的一个新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decreased LONP1 expression contributes to DNA damage and meiotic defects in oocytes

Meiotic defects in oocytes are the primary reason for decreased female fertility with advanced maternal age. In this study, we revealed that decreased expression of ATP-dependent Lon peptidase 1 (LONP1) in aged oocytes and oocyte-specific depletion of LONP1 disrupt oocyte meiotic progression accompanying with mitochondrial dysfunction. In addition, LONP1 downregulation increased oocyte DNA damage. Moreover, we demonstrated that splicing factor proline and glutamine rich directly interacts with LONP1 and mediate the effect of LONP1 depletion on meiotic progression in oocytes. In summary, our data suggest that decreased expression of LONP1 is involved in advanced maternal age-related meiosis defects and that LONP1 represents a new therapeutic target to improve aged oocyte quality.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.20
自引率
0.00%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Molecular Reproduction and Development takes an integrated, systems-biology approach to understand the dynamic continuum of cellular, reproductive, and developmental processes. This journal fosters dialogue among diverse disciplines through primary research communications and educational forums, with the philosophy that fundamental findings within the life sciences result from a convergence of disciplines. Increasingly, readers of the Journal need to be informed of diverse, yet integrated, topics impinging on their areas of interest. This requires an expansion in thinking towards non-traditional, interdisciplinary experimental design and data analysis.
×
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