Title of article
From Structure to Systems: High-Resolution, Quantitative Genetic Analysis of RNA Polymerase II
Author/Authors
Hannes Braberg، نويسنده , , Huiyan Jin، نويسنده , , Erica A. Moehle، نويسنده , , Yujia A. Chan، نويسنده , , Shuyi Wang، نويسنده , , Michael Shales، نويسنده , , Joris J. Benschop، نويسنده , , John H. Morris ، نويسنده , , Chenxi Qiu، نويسنده , , Fuqu Hu، نويسنده , , Leung K. Tang، نويسنده , , James S. Fraser، نويسنده , , Frank C.P. Holstege، نويسنده , , Philip Hieter، نويسنده , , Christine Guthrie، نويسنده , , Craig D. Kaplan، نويسنده , , Nevan J. Krogan، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
14
From page
775
To page
788
Abstract
RNA polymerase II (RNAPII) lies at the core of dynamic control of gene expression. Using 53 RNAPII point mutants, we generated a point mutant epistatic miniarray profile (pE-MAP) comprising ∼60,000 quantitative genetic interactions in Saccharomyces cerevisiae. This analysis enabled functional assignment of RNAPII subdomains and uncovered connections between individual regions and other protein complexes. Using splicing microarrays and mutants that alter elongation rates in vitro, we found an inverse relationship between RNAPII speed and in vivo splicing efficiency. Furthermore, the pE-MAP classified fast and slow mutants that favor upstream and downstream start site selection, respectively. The striking coordination of polymerization rate with transcription initiation and splicing suggests that transcription rate is tuned to regulate multiple gene expression steps. The pE-MAP approach provides a powerful strategy to understand other multifunctional machines at amino acid resolution.
Journal title
CELL
Serial Year
2013
Journal title
CELL
Record number
1021851
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