Suppr超能文献

c-Myc与人类核糖体DNA结合,并通过RNA聚合酶I刺激rRNA基因的转录。

c-Myc binds to human ribosomal DNA and stimulates transcription of rRNA genes by RNA polymerase I.

作者信息

Grandori Carla, Gomez-Roman Natividad, Felton-Edkins Zoe A, Ngouenet Celine, Galloway Denise A, Eisenman Robert N, White Robert J

机构信息

Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109-1024, USA.

出版信息

Nat Cell Biol. 2005 Mar;7(3):311-8. doi: 10.1038/ncb1224.

Abstract

c-Myc coordinates cell growth and division through a transcriptional programme that involves both RNA polymerase (Pol) II- and Pol III-transcribed genes. Here, we demonstrate that human c-Myc also directly enhances Pol I transcription of ribosomal RNA (rRNA) genes. rRNA synthesis and accumulation occurs rapidly following activation of a conditional MYC-ER allele (coding for a Myc-oestrogen-receptor fusion protein), is resistant to inhibition of Pol II transcription and is markedly reduced by c-MYC RNA interference. Furthermore, by using combined immunofluorescence and rRNA-FISH, we have detected endogenous c-Myc in nucleoli at sites of active ribosomal DNA (rDNA) transcription. Our data also show that c-Myc binds to specific consensus elements located in human rDNA and associates with the Pol I-specific factor SL1. The presence of c-Myc at specific sites on rDNA coincides with the recruitment of SL1 to the rDNA promoter and with increased histone acetylation. We propose that stimulation of rRNA synthesis by c-Myc is a key pathway driving cell growth and tumorigenesis.

摘要

c-Myc通过一个涉及RNA聚合酶(Pol)II和Pol III转录基因的转录程序来协调细胞生长和分裂。在此,我们证明人类c-Myc还直接增强核糖体RNA(rRNA)基因的Pol I转录。在条件性MYC-ER等位基因(编码Myc-雌激素受体融合蛋白)激活后,rRNA合成和积累迅速发生,对Pol II转录抑制具有抗性,并且通过c-MYC RNA干扰显著减少。此外,通过联合免疫荧光和rRNA-FISH,我们在活跃核糖体DNA(rDNA)转录位点的核仁中检测到内源性c-Myc。我们的数据还表明,c-Myc与位于人类rDNA中的特定共有元件结合,并与Pol I特异性因子SL1相关联。c-Myc在rDNA上的特定位点出现与SL1募集到rDNA启动子以及组蛋白乙酰化增加相吻合。我们提出,c-Myc对rRNA合成的刺激是驱动细胞生长和肿瘤发生的关键途径。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验