Cargando…

Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast

Although numerous regulatory connections between pre-mRNA splicing and chromatin have been demonstrated, the precise mechanisms by which chromatin factors influence spliceosome assembly and/or catalysis remain unclear. To probe the genetic network of pre-mRNA splicing in the fission yeast Schizosacc...

Descripción completa

Detalles Bibliográficos
Autores principales: Patrick, Kristin L., Ryan, Colm J., Xu, Jiewei, Lipp, Jesse J., Nissen, Kelly E., Roguev, Assen, Shales, Michael, Krogan, Nevan J., Guthrie, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380400/
https://www.ncbi.nlm.nih.gov/pubmed/25825871
http://dx.doi.org/10.1371/journal.pgen.1005074
_version_ 1782364329275817984
author Patrick, Kristin L.
Ryan, Colm J.
Xu, Jiewei
Lipp, Jesse J.
Nissen, Kelly E.
Roguev, Assen
Shales, Michael
Krogan, Nevan J.
Guthrie, Christine
author_facet Patrick, Kristin L.
Ryan, Colm J.
Xu, Jiewei
Lipp, Jesse J.
Nissen, Kelly E.
Roguev, Assen
Shales, Michael
Krogan, Nevan J.
Guthrie, Christine
author_sort Patrick, Kristin L.
collection PubMed
description Although numerous regulatory connections between pre-mRNA splicing and chromatin have been demonstrated, the precise mechanisms by which chromatin factors influence spliceosome assembly and/or catalysis remain unclear. To probe the genetic network of pre-mRNA splicing in the fission yeast Schizosaccharomyces pombe, we constructed an epistatic mini-array profile (E-MAP) and discovered many new connections between chromatin and splicing. Notably, the nucleosome remodeler SWI/SNF had strong genetic interactions with components of the U2 snRNP SF3 complex. Overexpression of SF3 components in ΔSWI/SNF cells led to inefficient splicing of many fission yeast introns, predominantly those with non-consensus splice sites. Deletion of SWI/SNF decreased recruitment of the splicing ATPase Prp2, suggesting that SWI/SNF promotes co-transcriptional spliceosome assembly prior to first step catalysis. Importantly, defects in SWI/SNF as well as SF3 overexpression each altered nucleosome occupancy along intron-containing genes, illustrating that the chromatin landscape both affects—and is affected by—co-transcriptional splicing.
format Online
Article
Text
id pubmed-4380400
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-43804002015-04-09 Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast Patrick, Kristin L. Ryan, Colm J. Xu, Jiewei Lipp, Jesse J. Nissen, Kelly E. Roguev, Assen Shales, Michael Krogan, Nevan J. Guthrie, Christine PLoS Genet Research Article Although numerous regulatory connections between pre-mRNA splicing and chromatin have been demonstrated, the precise mechanisms by which chromatin factors influence spliceosome assembly and/or catalysis remain unclear. To probe the genetic network of pre-mRNA splicing in the fission yeast Schizosaccharomyces pombe, we constructed an epistatic mini-array profile (E-MAP) and discovered many new connections between chromatin and splicing. Notably, the nucleosome remodeler SWI/SNF had strong genetic interactions with components of the U2 snRNP SF3 complex. Overexpression of SF3 components in ΔSWI/SNF cells led to inefficient splicing of many fission yeast introns, predominantly those with non-consensus splice sites. Deletion of SWI/SNF decreased recruitment of the splicing ATPase Prp2, suggesting that SWI/SNF promotes co-transcriptional spliceosome assembly prior to first step catalysis. Importantly, defects in SWI/SNF as well as SF3 overexpression each altered nucleosome occupancy along intron-containing genes, illustrating that the chromatin landscape both affects—and is affected by—co-transcriptional splicing. Public Library of Science 2015-03-31 /pmc/articles/PMC4380400/ /pubmed/25825871 http://dx.doi.org/10.1371/journal.pgen.1005074 Text en © 2015 Patrick et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Patrick, Kristin L.
Ryan, Colm J.
Xu, Jiewei
Lipp, Jesse J.
Nissen, Kelly E.
Roguev, Assen
Shales, Michael
Krogan, Nevan J.
Guthrie, Christine
Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast
title Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast
title_full Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast
title_fullStr Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast
title_full_unstemmed Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast
title_short Genetic Interaction Mapping Reveals a Role for the SWI/SNF Nucleosome Remodeler in Spliceosome Activation in Fission Yeast
title_sort genetic interaction mapping reveals a role for the swi/snf nucleosome remodeler in spliceosome activation in fission yeast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380400/
https://www.ncbi.nlm.nih.gov/pubmed/25825871
http://dx.doi.org/10.1371/journal.pgen.1005074
work_keys_str_mv AT patrickkristinl geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT ryancolmj geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT xujiewei geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT lippjessej geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT nissenkellye geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT roguevassen geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT shalesmichael geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT krogannevanj geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast
AT guthriechristine geneticinteractionmappingrevealsarolefortheswisnfnucleosomeremodelerinspliceosomeactivationinfissionyeast