Literature DB >> 17244735

Alterations in epigenetic modifications during oocyte growth in mice.

Shun-ichiro Kageyama1, Honglin Liu, Naoto Kaneko, Masatoshi Ooga, Masao Nagata, Fugaku Aoki.   

Abstract

During oocyte growth, chromatin structure is altered globally and gene expression is silenced. To investigate the involvement of epigenetic modifications in the regulation of these phenomena, changes in global DNA methylation and in various histone modifications, i.e. acetylation of H3K9, H3K18, H4K5, and H4K12, and methylation of H3K4 and H3K9, were examined during the growth of mouse oocytes. Immunocytochemical analysis revealed that the signal intensities of all these modifications increased during growth and that fully grown, germinal vesicle (GV)-stage oocytes showed the most modifications. Since acetylation of most of the lysine residues on histones and methylation of H3K4 are associated with active gene expression, the increased levels of these modifications do not seem to be associated with gene silencing in GV-stage oocytes. Given that there are two types of GV-stage oocytes with different chromatin configurations and transcriptional activities, the epigenetic modification statuses of these two types were compared. The levels of all the epigenetic modifications examined were higher in the SN(surrounded nucleolus)-type oocytes, in which highly condensed chromatin is concentrated in the area around the nucleolus and gene expression is silenced than in the NSN(not surrounded nucleolus)-type oocytes, in which less-condensed chromatin does not surround the nucleolus and gene expression is active. In addition, the expression levels of various enzymes that catalyze histone modifications were shown by RT-PCR to increase with oocyte growth. Taken together, the results show that all of the epigenetic modifications increased in a concerted manner during oocyte growth, and suggest that these increases are not associated with gene expression.

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Year:  2007        PMID: 17244735     DOI: 10.1530/REP-06-0025

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  57 in total

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2.  The competence of germinal vesicle oocytes is unrelated to nuclear chromatin configuration and strictly depends on cytoplasmic quantity and quality in the cat model.

Authors:  P Comizzoli; B S Pukazhenthi; D E Wildt
Journal:  Hum Reprod       Date:  2011-06-10       Impact factor: 6.918

3.  Fully-mature antral mouse oocytes are transcriptionally silent but their heterochromatin maintains a transcriptional permissive histone acetylation profile.

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Journal:  J Assist Reprod Genet       Date:  2011-04-06       Impact factor: 3.412

Review 4.  Epigenetic changes in mammalian gametes throughout their lifetime: the four seasons metaphor.

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Review 5.  The Epigenetics of Normal Pregnancy.

Authors:  Jonathan D Best; Nessa Carey
Journal:  Obstet Med       Date:  2013-03-01

6.  Histone acetyltransferase KAT8 is essential for mouse oocyte development by regulating reactive oxygen species levels.

Authors:  Shi Yin; Xiaohua Jiang; Hanwei Jiang; Qian Gao; Fang Wang; Suixing Fan; Teka Khan; Nazish Jabeen; Manan Khan; Asim Ali; Peng Xu; Tej K Pandita; Heng-Yu Fan; Yuanwei Zhang; Qinghua Shi
Journal:  Development       Date:  2017-05-15       Impact factor: 6.868

7.  Mammalian nucleolar protein DCAF13 is essential for ovarian follicle maintenance and oocyte growth by mediating rRNA processing.

Authors:  Jue Zhang; Yin-Li Zhang; Long-Wen Zhao; Jing-Xin Guo; Jia-Li Yu; Shu-Yan Ji; Lan-Rui Cao; Song-Ying Zhang; Li Shen; Xiang-Hong Ou; Heng-Yu Fan
Journal:  Cell Death Differ       Date:  2018-10-03       Impact factor: 15.828

Review 8.  Role of histone deacetylase 2 in epigenetics and cellular senescence: implications in lung inflammaging and COPD.

Authors:  Hongwei Yao; Irfan Rahman
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2012-07-27       Impact factor: 5.464

9.  Effects of In Vitro Maturation on Histone Acetylation in Metaphase II Oocytes and Early Cleavage Embryos.

Authors:  Ning Wang; Fang Le; Qi-Tao Zhan; Li Li; Min-Yue Dong; Guo-Lian Ding; Chen-Ming Xu; Shi-Wen Jiang; He-Feng Huang; Fan Jin
Journal:  Obstet Gynecol Int       Date:  2010-06-20

10.  MLL2 is required in oocytes for bulk histone 3 lysine 4 trimethylation and transcriptional silencing.

Authors:  Claudia V Andreu-Vieyra; Ruihong Chen; Julio E Agno; Stefan Glaser; Konstantinos Anastassiadis; A Francis Stewart; Martin M Matzuk
Journal:  PLoS Biol       Date:  2010-08-17       Impact factor: 8.029

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