| Literature DB >> 23744076 |
Kaspar Burger1, Bastian Mühl1, Michaela Rohrmoser1, Britta Coordes2, Martin Heidemann1, Markus Kellner1, Anita Gruber-Eber1, Vigo Heissmeyer3, Katja Strässer2, Dirk Eick4.
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.Entities:
Keywords: CDK (Cyclin-dependent Kinase); Flavopiridol; RNA Polymerase I; RNA Polymerase II; Ribosomal RNA Processing; Small Nucleolar RNA (snoRNA)
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Year: 2013 PMID: 23744076 PMCID: PMC3774383 DOI: 10.1074/jbc.M113.483719
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157