| Literature DB >> 30078214 |
Chunling Li1, Feiyang Diao1,2, Danhong Qiu1, Manxi Jiang3, Xiaoyan Li1,4, Longsen Han1, Ling Li1, Xiaojing Hou1, Juan Ge1, Xianghong Ou3, Jiayin Liu1,2, Qiang Wang1.
Abstract
SET-domain-containing 2 (SETD2), a member of the histone lysine methyltransferase family, has been reported to be involved in multiple biological processes. However, the function of SETD2 during oocyte maturation has not been addressed. In this study, we find that mouse oocytes are incapable of progressing through meiosis completely once SETD2 is specifically depleted. These oocytes present an abnormal spindle morphology and deficient chromosome movement, with disrupted kinetochore-microtubule attachments, consequently producing aneuploidy eggs. In line with this, the BubR1 signal is markedly elevated in metaphase kinetochores of oocytes with SETD2 depletion, indicative of the activation of spindle assembly checkpoint. In addition, we note that loss of SETD2 results in a drastic decrease in the trimethylation level of H3K36 in oocytes. Collectively, our data demonstrate that SETD2 is required for oocyte maturation and indicate a novel mechanism controlling the meiotic apparatus.Entities:
Keywords: SETD2; histone methylation; meiosis; oocyte; spindle
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Year: 2018 PMID: 30078214 DOI: 10.1002/jcp.26836
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384