Inactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.

Faithful chromosome segregation is fundamentally important for the maintenance of genome integrity and ploidy. By isolating conditional mutants defective in chromosome segregation in the fission yeast Schizosaccharomyces pombe, we identified a role for the essential gene pfs2 in chromosome dynamics....

Full description

Bibliographic Details
Main Authors: Wang, S, Asakawa, K, Win, T, Toda, T, Norbury, C
Format: Journal article
Language:English
Published: 2005
_version_ 1826287606643556352
author Wang, S
Asakawa, K
Win, T
Toda, T
Norbury, C
author_facet Wang, S
Asakawa, K
Win, T
Toda, T
Norbury, C
author_sort Wang, S
collection OXFORD
description Faithful chromosome segregation is fundamentally important for the maintenance of genome integrity and ploidy. By isolating conditional mutants defective in chromosome segregation in the fission yeast Schizosaccharomyces pombe, we identified a role for the essential gene pfs2 in chromosome dynamics. In the absence of functional Pfs2, chromosomal attachment to the mitotic spindle was defective, with consequent chromosome missegregation. Under these circumstances, multiple intracellular foci of spindle checkpoint proteins Bub1 and Mad2 were seen, and deletion of bub1 exacerbated the mitotic defects and the loss of cell viability that resulted from the loss of pfs2 function. Progression from G1 into S phase following release from nitrogen starvation also required pfs2+ function. The product of the orthologous Saccharomyces cerevisiae gene PFS2 is a component of a multiprotein complex required for 3'-end cleavage and polyadenylation of pre-mRNAs and, in keeping with the conservation of this essential function, an S. pombe pfs2 mutant was defective in mRNA 3'-end processing. Mutations in pfs2 were suppressed by overexpression of the putative mRNA 3'-end cleavage factor Cft1. These data suggest unexpected links between mRNA 3'-end processing and chromosome replication and segregation.
first_indexed 2024-03-07T02:01:11Z
format Journal article
id oxford-uuid:9d69bff8-7dde-4b2c-b6cc-70df43de762e
institution University of Oxford
language English
last_indexed 2024-03-07T02:01:11Z
publishDate 2005
record_format dspace
spelling oxford-uuid:9d69bff8-7dde-4b2c-b6cc-70df43de762e2022-03-27T00:42:56ZInactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9d69bff8-7dde-4b2c-b6cc-70df43de762eEnglishSymplectic Elements at Oxford2005Wang, SAsakawa, KWin, TToda, TNorbury, CFaithful chromosome segregation is fundamentally important for the maintenance of genome integrity and ploidy. By isolating conditional mutants defective in chromosome segregation in the fission yeast Schizosaccharomyces pombe, we identified a role for the essential gene pfs2 in chromosome dynamics. In the absence of functional Pfs2, chromosomal attachment to the mitotic spindle was defective, with consequent chromosome missegregation. Under these circumstances, multiple intracellular foci of spindle checkpoint proteins Bub1 and Mad2 were seen, and deletion of bub1 exacerbated the mitotic defects and the loss of cell viability that resulted from the loss of pfs2 function. Progression from G1 into S phase following release from nitrogen starvation also required pfs2+ function. The product of the orthologous Saccharomyces cerevisiae gene PFS2 is a component of a multiprotein complex required for 3'-end cleavage and polyadenylation of pre-mRNAs and, in keeping with the conservation of this essential function, an S. pombe pfs2 mutant was defective in mRNA 3'-end processing. Mutations in pfs2 were suppressed by overexpression of the putative mRNA 3'-end cleavage factor Cft1. These data suggest unexpected links between mRNA 3'-end processing and chromosome replication and segregation.
spellingShingle Wang, S
Asakawa, K
Win, T
Toda, T
Norbury, C
Inactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.
title Inactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.
title_full Inactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.
title_fullStr Inactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.
title_full_unstemmed Inactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.
title_short Inactivation of the pre-mRNA cleavage and polyadenylation factor Pfs2 in fission yeast causes lethal cell cycle defects.
title_sort inactivation of the pre mrna cleavage and polyadenylation factor pfs2 in fission yeast causes lethal cell cycle defects
work_keys_str_mv AT wangs inactivationofthepremrnacleavageandpolyadenylationfactorpfs2infissionyeastcauseslethalcellcycledefects
AT asakawak inactivationofthepremrnacleavageandpolyadenylationfactorpfs2infissionyeastcauseslethalcellcycledefects
AT wint inactivationofthepremrnacleavageandpolyadenylationfactorpfs2infissionyeastcauseslethalcellcycledefects
AT todat inactivationofthepremrnacleavageandpolyadenylationfactorpfs2infissionyeastcauseslethalcellcycledefects
AT norburyc inactivationofthepremrnacleavageandpolyadenylationfactorpfs2infissionyeastcauseslethalcellcycledefects