Maternal epigenetic factors in embryonic and postnatal development

Author:

Nishimura Hiromi1,Ikawa Yayoi1,Kajikawa Eriko1,Shimizu‐Mizuno Natsumi1,Hiver Sylvain1,Tabata‐Okamoto Namine2,Mori Masashi2,Kitajima Tomoya23ORCID,Hayashi Tetsutaro4,Yoshimura Mika4,Umeda Mana4,Nikaido Itoshi45,Kurokawa Mineo6,Watanabe Toshio7,Hamada Hiroshi1ORCID

Affiliation:

1. Laboratory for Organismal Patterning RIKEN Center for Biosystems Dynamics Research, 2‐2‐3 Minatojima‐minamimachi, Chuo‐ku Kobe Hyogo 650‐0047 Japan

2. Laboratory of Chromosome Segregation RIKEN Center for Biosystems Dynamics Research Kobe Hyogo Japan

3. Graduate School of Biostudies Kyoto University Kyoto Japan

4. Laboratory of Bioinformatics Research RIKEN Center for Biosystems Dynamics Research Kobe Hyogo Japan

5. Department of Functional Genome Informatics, Division of Biological Data Science, Medical Research Institute Tokyo Medical and Dental University, Bunkyo‐ku Tokyo Japan

6. Department of Hematology and Oncology, Graduate School of Medicine The University of Tokyo, 7‐3‐1 Hongo, Bunkyo‐ku Tokyo 113‐8655 Japan

7. Department of Biological Science, Graduate School of Humanities and Science Nara Women's University, Kita‐uoya Nishi‐machi Nara 630‐8506 Japan

Abstract

AbstractMaternal factors present in oocytes and surrounding granulosa cells influence early development of embryos. In this study, we searched for epigenetic regulators that are expressed in oocytes and/or granulosa cells. Some of the 120 epigenetic regulators examined were expressed specifically in oocytes and/or granulosa cells. When their expression was examined in young versus aged oocytes or granulosa cells, many were significantly up‐ or downregulated in aged cells. The maternal role of six genes in development was investigated by generating oocyte‐specific knock‐out (MKO) mice. Two genes (Mllt10, Kdm2b) did not show maternal effects on later development, whereas maternal effects were evident for Kdm6a, Kdm4a, Prdm3, and Prdm16 for MKO female mice. Offspring from Kdm6a MKO mice underwent perinatal lethality at a higher rate. Pups derived from Prdm3;Prdm16 double MKO showed a higher incidence of postnatal death. Finally, embryos derived from Kdm4a MKO mice showed early developmental defects as early as the peri‐implantation stage. These results suggest that many of maternal epigenetic regulators undergo differential expression upon aging. Some, such as Kdm4a, Kdm6a, Prdm3, and Prdm16, have maternal role in later embryonic or postnatal development.

Funder

Core Research for Evolutional Science and Technology

Ministry of Education, Culture, Sports, Science and Technology

RIKEN

Publisher

Wiley

Subject

Cell Biology,Genetics

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3