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细胞周期蛋白依赖性激酶 9 将 RNA 聚合酶 II 转录与核糖体 RNA 的加工联系起来。

Cyclin-dependent kinase 9 links RNA polymerase II transcription to processing of ribosomal RNA.

机构信息

From the Department of Molecular Epigenetics, Helmholtz Center Munich, Center for Integrated Protein Science Munich, Marchioninistrasse 25, 81377 Munich, Germany.

Gene Center and Department of Biochemistry, Center for Integrated Protein Science Munich, Ludwig Maximilians University of Munich, Feodor-Lynen-Strasse 25, 81377 Munich, Germany, and.

出版信息

J Biol Chem. 2013 Jul 19;288(29):21173-21183. doi: 10.1074/jbc.M113.483719. Epub 2013 Jun 6.

Abstract

Ribosome biogenesis is a process required for cellular growth and proliferation. Processing of ribosomal RNA (rRNA) is highly sensitive to flavopiridol, a specific inhibitor of cyclin-dependent kinase 9 (Cdk9). Cdk9 has been characterized as the catalytic subunit of the positive transcription elongation factor b (P-TEFb) of RNA polymerase II (RNAPII). Here we studied the connection between RNAPII transcription and rRNA processing. We show that inhibition of RNAPII activity by α-amanitin specifically blocks processing of rRNA. The block is characterized by accumulation of 3' extended unprocessed 47 S rRNAs and the entire inhibition of other 47 S rRNA-specific processing steps. The transcription rate of rRNA is moderately reduced after inhibition of Cdk9, suggesting that defective 3' processing of rRNA negatively feeds back on RNAPI transcription. Knockdown of Cdk9 caused a strong reduction of the levels of RNAPII-transcribed U8 small nucleolar RNA, which is essential for 3' rRNA processing in mammalian cells. Our data demonstrate a pivotal role of Cdk9 activity for coupling of RNAPII transcription with small nucleolar RNA production and rRNA processing.

摘要

核糖体生物发生是细胞生长和增殖所必需的过程。核糖体 RNA(rRNA)的加工对 flavopiridol(一种细胞周期蛋白依赖性激酶 9(Cdk9)的特异性抑制剂)高度敏感。Cdk9 已被鉴定为 RNA 聚合酶 II(RNAPII)的正转录延伸因子 b(P-TEFb)的催化亚基。在这里,我们研究了 RNAPII 转录与 rRNA 加工之间的联系。我们表明,α-鹅膏蕈碱抑制 RNAPII 活性会特异性阻断 rRNA 的加工。该阻断的特征是 3'延伸的未加工 47S rRNA 的积累和所有其他 47S rRNA 特异性加工步骤的完全抑制。Cdk9 抑制后 rRNA 的转录率适度降低,表明 rRNA 的 3'加工缺陷会对 RNAPI 转录产生负反馈。Cdk9 的敲低导致 RNAPII 转录的 U8 小核仁 RNA 水平大幅降低,这对哺乳动物细胞中 3' rRNA 加工至关重要。我们的数据表明 Cdk9 活性在将 RNAPII 转录与小核仁 RNA 产生和 rRNA 加工偶联中起着关键作用。

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