JHDM1B/FBXL10 is a nucleolar protein that represses transcription of ribosomal RNA genes

被引:239
作者
Frescas, David [1 ]
Guardavaccaro, Daniele [1 ]
Bassermann, Florian [1 ]
Koyama-Nasu, Ryo [1 ]
Pagano, Michele [1 ]
机构
[1] NYU, Sch Med, Dept Pathol, Inst Canc, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature06255
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
JHDM1B is an evolutionarily conserved and ubiquitously expressed member of the JHDM (JmjC-domain-containing histone demethylase) family(1-3). Because it contains an F-box motif, this protein is also known as FBXL10 (ref. 4). With the use of a genome-wide RNAi screen, the JHDM1B worm orthologue (T26A5.5) was identified as a gene that regulates growth(5). In the mouse, four independent screens have identified JHDM1B as a putative tumour suppressor by retroviral insertion analysis(6-9). Here we identify human JHDM1B as a nucleolar protein and show that JHDM1B preferentially binds the transcribed region of ribosomal DNA to repress the transcription of ribosomal RNA genes. We also show that repression of ribosomal RNA genes by JHDM1B is dependent on its JmjC domain, which is necessary for the specific demethylation of trimethylated lysine 4 on histone H3 in the nucleolus. In agreement with the notion that ribosomal RNA synthesis and cell growth are coupled processes, we show a JmjC-domain-dependent negative effect of JHDM1B on cell size and cell proliferation. Because aberrant ribosome biogenesis and the disruption of epigenetic control mechanisms contribute to cellular transformation, these results, together with the low levels of JHDM1B expression found in aggressive brain tumours, suggest a role for JHDM1B in cancer development.
引用
收藏
页码:309 / U17
页数:6
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