【講演案内】
※岩渕様には、翌日の第15回FBS研究教育交流会にても生命OBとして、ご講演いただきます。
演者：岩渕ー土井真木子（ペンシルバニア大学・ Kenneth Zaret Lab/研究員）
所属：ペンシルバニア大学・Cincinnati Children's Hospital Medical Center, USA (starting in Nov 2017)
演題："Developmental Role and Mechanistic Insight into Chromatin Opening by Pioneer Factor"
要旨：
Gene regulation occurs in the context of chromatin, the complex of DNA and histone proteins that makes up nucleosomes, where linker histones stabilize a repressive, closed configuration. A distinct combination of transcription factors is necessary to elicit cell fate changes in embryonic development and cellular reprogramming. Within each group of fate-changing transcription factors, a subset called "pioneer factors" are dominant in their ability to engage silent chromatin and recruit other transcription factors, thereby imparting new function to regulatory DNA sequences. However, the molecular mechanisms by which pioneer factors open chromatin remains unclear. Here we demonstrate that a pioneer factor FoxA, but not ATP-dependent chromatin remodelers, opens unmodified chromatin compacted with linker histones, which then allows chromatin remodelers to further open chromatin. We identified a chromatin opening domain in FoxA C-terminus that potentially interacts with core histones. When we deleted the chromatin opening domain in the mouse FoxA2 genomic locus, but kept the other FoxA2 parts intact, including the DNA binding and transactivation domains, chromatin opening and embryonic development were markedly affected. These studies provide mechanistic insight into chromatin opening and can ultimately enhance our ability to control chromatin state at will.
世話人：橋本昌和 （生命機能研究科初期胚発生研究室(佐々木研)・助教）
Tel：06-6879-4659（ex.4659）
E-mail：mhashimo@fbs.osaka-u.ac.jp
※岩渕様には、翌日の第15回FBS研究教育交流会にても生命OBとして、ご講演いただきます。
演者：岩渕ー土井真木子（ペンシルバニア大学・ Kenneth Zaret Lab/研究員）
所属：ペンシルバニア大学・Cincinnati Children's Hospital Medical Center, USA (starting in Nov 2017)
演題："Developmental Role and Mechanistic Insight into Chromatin Opening by Pioneer Factor"
要旨：
Gene regulation occurs in the context of chromatin, the complex of DNA and histone proteins that makes up nucleosomes, where linker histones stabilize a repressive, closed configuration. A distinct combination of transcription factors is necessary to elicit cell fate changes in embryonic development and cellular reprogramming. Within each group of fate-changing transcription factors, a subset called "pioneer factors" are dominant in their ability to engage silent chromatin and recruit other transcription factors, thereby imparting new function to regulatory DNA sequences. However, the molecular mechanisms by which pioneer factors open chromatin remains unclear. Here we demonstrate that a pioneer factor FoxA, but not ATP-dependent chromatin remodelers, opens unmodified chromatin compacted with linker histones, which then allows chromatin remodelers to further open chromatin. We identified a chromatin opening domain in FoxA C-terminus that potentially interacts with core histones. When we deleted the chromatin opening domain in the mouse FoxA2 genomic locus, but kept the other FoxA2 parts intact, including the DNA binding and transactivation domains, chromatin opening and embryonic development were markedly affected. These studies provide mechanistic insight into chromatin opening and can ultimately enhance our ability to control chromatin state at will.
世話人：橋本昌和 （生命機能研究科初期胚発生研究室(佐々木研)・助教）
Tel：06-6879-4659（ex.4659）
E-mail：mhashimo@fbs.osaka-u.ac.jp