Serine-7 of the RNA Polymerase II CTD Is Specifically Required for snRNA Gene Expression

Author:

Egloff Sylvain12,O'Reilly Dawn12,Chapman Rob D.12,Taylor Alice12,Tanzhaus Katrin12,Pitts Laura12,Eick Dirk12,Murphy Shona12

Affiliation:

1. Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.

2. Institute of Clinical Molecular Biology and Tumour Genetics, Gesellschaft fuer Strahlung Forschung (GSF)-Research Centre of Environment and Health, Munich Center for Integrated Protein Science (CiPSM), Marchioninistrasse 25, 81377 Munich, Germany.

Abstract

RNA polymerase II (Pol II) transcribes genes that encode proteins and noncoding small nuclear RNAs (snRNAs). The carboxyl-terminal repeat domain (CTD) of the largest subunit of mammalian RNA Pol II, comprising tandem repeats of the heptapeptide consensus Tyr 1 -Ser 2 -Pro 3 -Thr 4 -Ser 5 -Pro 6 -Ser 7 , is required for expression of both gene types. We show that mutation of serine-7 to alanine causes a specific defect in snRNA gene expression. We also present evidence that phosphorylation of serine-7 facilitates interaction with the snRNA gene–specific Integrator complex. These findings assign a biological function to this amino acid and highlight a gene type–specific requirement for a residue within the CTD heptapeptide, supporting the existence of a CTD code.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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