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Reference - PMID:22508988 - Separate domains of fission yeast Cdk9 (P-TEFb) are required for capping enzyme recruitment and primed (Ser7-phosphorylated) Rpb1 carboxyl-terminal domain substrate recognition.

Reference summary

PubMed ID
PMID:22508988
Title
Separate domains of fission yeast Cdk9 (P-TEFb) are required for capping enzyme recruitment and primed (Ser7-phosphorylated) Rpb1 carboxyl-terminal domain substrate recognition.
Authors
St Amour CV, Sansó M, Bösken CA, Lee KM, Larochelle S, Zhang C, Shokat KM, Geyer M, Fisher RP
Citation
Mol Cell Biol 2012 Jul;32(13):2372-83
Publication year
2012
Abstract
In fission yeast, discrete steps in mRNA maturation and synthesis depend on a complex containing the 5'-cap methyltransferase Pcm1 and Cdk9, which phosphorylates the RNA polymerase II (Pol II) carboxyl-terminal domain (CTD) and the processivity factor Spt5 to promote transcript elongation. Here we show that a Cdk9 carboxyl-terminal extension, distinct from the catalytic domain, mediates binding to both Pcm1 and the Pol II CTD. Removal of this segment diminishes Cdk9/Pcm1 chromatin recruitment and Spt5 phosphorylation in vivo and leads to slow growth and hypersensitivity to cold temperature, nutrient limitation, and the IMP dehydrogenase inhibitor mycophenolic acid (MPA). These phenotypes, and the Spt5 phosphorylation defect, are suppressed by Pcm1 overproduction, suggesting that normal transcript elongation and gene expression depend on physical linkage between Cdk9 and Pcm1. The extension is dispensable, however, for recognition of CTD substrates "primed" by Mcs6 (Cdk7). On defined peptide substrates in vitro, Cdk9 prefers CTD repeats phosphorylated at Ser7 over unmodified repeats. In vivo, Ser7 phosphorylation depends on Mcs6 activity, suggesting a conserved mechanism, independent of chromatin recruitment, to order transcriptional CDK functions. Therefore, fission yeast Cdk9 comprises a catalytic domain sufficient for primed substrate recognition and a multivalent recruitment module that couples transcription with capping.

Annotation

GO molecular function

GO:0140463 - chromatin-protein adaptor activity

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GO:0005515 - protein binding

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GO:0004674 - protein serine/threonine kinase activity

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Modification

MOD:00046 - O-phospho-L-serine

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Multi-locus phenotype

FYPO:0000705 - abolished protein-protein interaction

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Single locus phenotype

FYPO:0000705 - abolished protein-protein interaction

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FYPO:0000080 - decreased cell population growth at low temperature

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FYPO:0006631 - decreased protein localization to chromatin

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FYPO:0002679 - decreased protein phosphorylation

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FYPO:0001355 - decreased vegetative cell population growth

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FYPO:0002141 - normal cell population growth at low temperature

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FYPO:0007074 - normal growth on mycophenolic acid

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FYPO:0003075 - normal protein kinase activity

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FYPO:0004083 - normal protein level

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FYPO:0001357 - normal vegetative cell population growth

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FYPO:0003670 - sensitive to mycophenolic acid

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FYPO:0006821 - slow vegetative cell growth

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