High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop.
The active sites of multisubunit RNA polymerases have a "trigger loop" (TL) that multitasks in substrate selection, catalysis, and translocation. To dissect the Saccharomyces cerevisiae RNA polymerase II TL at individual-residue resolution, we quantitatively phenotyped nearly all TL single...
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2016-11-01
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doaj-0093dec7c23e444383965144785bda192020-11-25T01:16:11ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042016-11-011211e100632110.1371/journal.pgen.1006321High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop.Chenxi QiuOlivia C ErinneJui M DavePing CuiHuiyan JinNandhini MuthukrishnanLeung K TangSabareesh Ganesh BabuKenny C LamPaul J VandeventerRalf StrohnerJan Van den BrulleSing-Hoi SzeCraig D KaplanThe active sites of multisubunit RNA polymerases have a "trigger loop" (TL) that multitasks in substrate selection, catalysis, and translocation. To dissect the Saccharomyces cerevisiae RNA polymerase II TL at individual-residue resolution, we quantitatively phenotyped nearly all TL single variants en masse. Three mutant classes, revealed by phenotypes linked to transcription defects or various stresses, have distinct distributions among TL residues. We find that mutations disrupting an intra-TL hydrophobic pocket, proposed to provide a mechanism for substrate-triggered TL folding through destabilization of a catalytically inactive TL state, confer phenotypes consistent with pocket disruption and increased catalysis. Furthermore, allele-specific genetic interactions among TL and TL-proximal domain residues support the contribution of the funnel and bridge helices (BH) to TL dynamics. Our structural genetics approach incorporates structural and phenotypic data for high-resolution dissection of transcription mechanisms and their evolution, and is readily applicable to other essential yeast proteins.http://europepmc.org/articles/PMC5127505?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chenxi Qiu Olivia C Erinne Jui M Dave Ping Cui Huiyan Jin Nandhini Muthukrishnan Leung K Tang Sabareesh Ganesh Babu Kenny C Lam Paul J Vandeventer Ralf Strohner Jan Van den Brulle Sing-Hoi Sze Craig D Kaplan |
spellingShingle |
Chenxi Qiu Olivia C Erinne Jui M Dave Ping Cui Huiyan Jin Nandhini Muthukrishnan Leung K Tang Sabareesh Ganesh Babu Kenny C Lam Paul J Vandeventer Ralf Strohner Jan Van den Brulle Sing-Hoi Sze Craig D Kaplan High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop. PLoS Genetics |
author_facet |
Chenxi Qiu Olivia C Erinne Jui M Dave Ping Cui Huiyan Jin Nandhini Muthukrishnan Leung K Tang Sabareesh Ganesh Babu Kenny C Lam Paul J Vandeventer Ralf Strohner Jan Van den Brulle Sing-Hoi Sze Craig D Kaplan |
author_sort |
Chenxi Qiu |
title |
High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop. |
title_short |
High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop. |
title_full |
High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop. |
title_fullStr |
High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop. |
title_full_unstemmed |
High-Resolution Phenotypic Landscape of the RNA Polymerase II Trigger Loop. |
title_sort |
high-resolution phenotypic landscape of the rna polymerase ii trigger loop. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Genetics |
issn |
1553-7390 1553-7404 |
publishDate |
2016-11-01 |
description |
The active sites of multisubunit RNA polymerases have a "trigger loop" (TL) that multitasks in substrate selection, catalysis, and translocation. To dissect the Saccharomyces cerevisiae RNA polymerase II TL at individual-residue resolution, we quantitatively phenotyped nearly all TL single variants en masse. Three mutant classes, revealed by phenotypes linked to transcription defects or various stresses, have distinct distributions among TL residues. We find that mutations disrupting an intra-TL hydrophobic pocket, proposed to provide a mechanism for substrate-triggered TL folding through destabilization of a catalytically inactive TL state, confer phenotypes consistent with pocket disruption and increased catalysis. Furthermore, allele-specific genetic interactions among TL and TL-proximal domain residues support the contribution of the funnel and bridge helices (BH) to TL dynamics. Our structural genetics approach incorporates structural and phenotypic data for high-resolution dissection of transcription mechanisms and their evolution, and is readily applicable to other essential yeast proteins. |
url |
http://europepmc.org/articles/PMC5127505?pdf=render |
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