Human PIH1 associates with histone H4 to mediate the glucose-dependent enhancement of pre-rRNA synthesis
Author(s) -
Niu Zhai,
Zhongliang Zhao,
Mo-Bin Cheng,
Yuwei Di,
Haixia Yan,
Chunyu Cao,
Hui Dai,
Zhang Ye,
Yufei Shen
Publication year - 2012
Publication title -
journal of molecular cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.825
H-Index - 62
eISSN - 1674-2788
pISSN - 1759-4685
DOI - 10.1093/jmcb/mjs003
Subject(s) - ribosome biogenesis , chromatin remodeling , biology , chromatin immunoprecipitation , histone h4 , ribosomal rna , chromatin , microbiology and biotechnology , histone , gene , ribosome , genetics , rna , promoter , gene expression
Ribosome biogenesis is critical in the growth of eukaryotic cells, in which the synthesis of precursor ribosomal RNA is the first and rate-limiting step. Here, we show that human PIH1 domain-containing protein 1 (PIH1) interacts directly with histone H4 and recruits the Brg1-SWI/SNF complex via SNF5 to human rRNA genes. This process is likely involved in PIH1-dependent DNase I-hypersensitive chromatin remodeling at the core promoter of the rRNA genes. PIH1 mediates the occupancy of not only the Brg1 complex but also the Pol I complex at the core promoter and enhances transcription initiation of rRNA genes. Additionally, the interaction between PIH1 and H4K16 expels TIP5, a component of the silencing nucleolar remodeling complex (NoRC), from the core region, suggesting that PIH1 is involved in the derepression of NoRC-silenced rRNA genes. These data indicate that PIH1 is a positive regulator of human rRNA genes and is of great importance for the recovery of human cells from nutrient starvation and the transition to glucose-induced exponential growth in vivo.
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