Seminar & Symposium/Admissions

セミナー・シンポジウム及び入試情報

2019-02-20

最先端研究セミナー

 

講演者: 浦 聖恵 (千葉大学大学院 理学研究員 生物学研究部門  教授)

演題: Chromatin modification: from structure and function

 

日時: 2019年 2月20日(水) 12:00-13:00

会場: 発生医学研究所1階 カンファレンス室

 

Abstract:

The basic subunit of chromatin, the nucleosome, consists of DNA wrapped around an octamer of four core histones: H2A, H2B, H3 and H4, and linker histone H1. Chromatin modification, such as histone modifications and DNA methylation, are catalyzed and recognized by specific proteins, establishing unique modification patterns that act as chromatin signals. To understand the mechanism of regulation of chromatin modification, as well as their function in development, we have been studying on the structural and functional transition of chromatin both in the reconstituted chromatin and in the nucleus.

More recently, we demonstrated that a H3K36 methyltransferase NSD2, also known as WHSC1 or MMSET, functions for transcriptional regulation and that the NSD2 deficiency is responsible for Wolf-Hirschhorn syndrome (WHS). NSD2 is required for normal hematopoietic differentiation, especially for B cell development. Here, we show that mouse Nsd2 is involved in V(D)J recombination during B-cell development, suggesting the functional link between Nsd2 and DNA repair.

Transcription-associated DNA repair mediated by histone H3K36 methylation will be discussed.

 

Reference:

Saeki H., Ohsumi  K, Aihara  H, Ito T, Hirose  S, *Ura  K. and  Kaneda  Y.   Linker  histone  variants  control chromatin  dynamics during early embryogenesis.  PNAS. 102, 5697-5702,  2005

Nimura K., * Ura K., Shiratori  H. Schwartz  R. Ikawa M. Okabe M. and *Kaneda  Y. A histone H3 lysine 36 trimethyltransferase  linkes Nkx2-5 to Wolf-Hirschhorn  syndrome.  Nature, 460, 287-291, 2009

Kashiwagi K., Nimura  K.,   *Ura  K. and *Kaneda  Y. DNA  methyltransferase   3b preferentially   associates with condensed  chromatin.  Nucleic Acids Res., 39, 874-888, 2011

Campos-Sanchez E. Deleyto-Seldas NDominguez VCarrillo-de-Santa-Pau EUra K, 他11名, Cobaleda C*. Wolf-Hirschhorn Syndrome Candidate 1 Is Necessary for Correct Hematopoietic and B Cell Development., Cell Rep. 19, 1586-1601, 2017

 

担当分野:多能性幹細胞 丹羽(内線:6620)

※ 詳細はこちらから

Copyright © Kumamoto University All Rights Reserved.