Frescas David, Guardavaccaro Daniele, Bassermann Florian, Koyama-Nasu Ryo, Pagano Michele
Department of Pathology, NYU Cancer Institute, New York University School of Medicine, 550 First Avenue, New York, New York 10016, USA.
Nature. 2007 Nov 8;450(7167):309-13. doi: 10.1038/nature06255.
JHDM1B is an evolutionarily conserved and ubiquitously expressed member of the JHDM (JmjC-domain-containing histone demethylase) family. 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. In the mouse, four independent screens have identified JHDM1B as a putative tumour suppressor by retroviral insertion analysis. 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.
JHDM1B是含JmjC结构域的组蛋白去甲基化酶(JHDM)家族中一个在进化上保守且广泛表达的成员。由于它含有一个F-box基序,该蛋白也被称为FBXL10(参考文献4)。通过全基因组RNA干扰筛选,JHDM1B在蠕虫中的直系同源物(T26A5.5)被鉴定为一个调控生长的基因。在小鼠中,四项独立筛选通过逆转录病毒插入分析将JHDM1B鉴定为一个假定的肿瘤抑制因子。在此,我们将人类JHDM1B鉴定为一种核仁蛋白,并表明JHDM1B优先结合核糖体DNA的转录区域以抑制核糖体RNA基因的转录。我们还表明,JHDM1B对核糖体RNA基因的抑制作用依赖于其JmjC结构域,该结构域对于核仁中组蛋白H3上三甲基化赖氨酸4的特异性去甲基化是必需的。与核糖体RNA合成和细胞生长是相互关联的过程这一观点一致,我们展示了JHDM1B对细胞大小和细胞增殖具有依赖于JmjC结构域的负向作用。由于异常的核糖体生物合成和表观遗传控制机制的破坏有助于细胞转化,这些结果,连同在侵袭性脑肿瘤中发现的JHDM1B低表达水平,提示JHDM1B在癌症发展中发挥作用。