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Article: Identification of novel factors involved in or regulating initiation of DNA replication by a genome-wide phenotypic screen in Saccharomyces cerevisiae

TitleIdentification of novel factors involved in or regulating initiation of DNA replication by a genome-wide phenotypic screen in Saccharomyces cerevisiae
Authors
KeywordsCTF18
CTF1
Plasmid loss
Phenotypic screen
Budding yeast
DNA replication initiation
Issue Date2010
Citation
Cell Cycle, 2010, v. 9, n. 21, p. 4399-4410 How to Cite?
AbstractDNA replication in eukaryotic cells is tightly regulated to ensure faithful inheritance of the genetic material. While the replicators, replication origins and many replication-initiation proteins in Saccharomyces cerevisiae have been identified and extensively studied, the detailed mechanism that controls the initiation of DNA replication is still not well understood. It is likely that some factors involved in or regulating the initiation of DNA replication have not been discovered. To identify novel DNA replication-initiation proteins and their regulators, we developed a sensitive and comprehensive phenotypic screen by combining several established genetic strategies including plasmid loss assays with plasmids containing a single versus multiple replication origins and colony color sectoring assays. We isolated dozen of mutants in previously known initiation proteins and identified several novel factors, including Ctf1p Ctf3p, Ctf4p, Ctf18p, Adk1p and Cdc60p, whose mutants lose plasmid containing a single replication origin at high rates but lose plasmid carrying multiple replication origins at lower rates. We also show that overexpression of replication initiation proteins causes synthetic dosage lethality or growth defects in ctf1 and ctf18 mutants and that Ctf1p and Ctf18p physically interact with ORC, Cdt1p and MCM proteins. Furthermore, depletion of both Ctf1p and Ctf18p prevents S phase entry, retards S phase progression, and reduces pre-RC formation during the M-to-G1 transition. These data suggest that Ctf1p and Ctf18p together play important roles in regulating the initiation of DNA replication. © 2010 Landes Bioscience.
Persistent Identifierhttp://hdl.handle.net/10722/256019
ISSN
2023 Impact Factor: 3.4
2023 SCImago Journal Rankings: 0.947
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMa, Lijuan-
dc.contributor.authorZhai, Yuanliang-
dc.contributor.authorFeng, Daorong-
dc.contributor.authorChan, Tsz Choi-
dc.contributor.authorLu, Yongjun-
dc.contributor.authorFu, Xinrong-
dc.contributor.authorWang, Jiafeng-
dc.contributor.authorChen, Yanhong-
dc.contributor.authorLi, Jianna-
dc.contributor.authorXu, Ke-
dc.contributor.authorLiang, Chun-
dc.date.accessioned2018-07-16T06:14:21Z-
dc.date.available2018-07-16T06:14:21Z-
dc.date.issued2010-
dc.identifier.citationCell Cycle, 2010, v. 9, n. 21, p. 4399-4410-
dc.identifier.issn1538-4101-
dc.identifier.urihttp://hdl.handle.net/10722/256019-
dc.description.abstractDNA replication in eukaryotic cells is tightly regulated to ensure faithful inheritance of the genetic material. While the replicators, replication origins and many replication-initiation proteins in Saccharomyces cerevisiae have been identified and extensively studied, the detailed mechanism that controls the initiation of DNA replication is still not well understood. It is likely that some factors involved in or regulating the initiation of DNA replication have not been discovered. To identify novel DNA replication-initiation proteins and their regulators, we developed a sensitive and comprehensive phenotypic screen by combining several established genetic strategies including plasmid loss assays with plasmids containing a single versus multiple replication origins and colony color sectoring assays. We isolated dozen of mutants in previously known initiation proteins and identified several novel factors, including Ctf1p Ctf3p, Ctf4p, Ctf18p, Adk1p and Cdc60p, whose mutants lose plasmid containing a single replication origin at high rates but lose plasmid carrying multiple replication origins at lower rates. We also show that overexpression of replication initiation proteins causes synthetic dosage lethality or growth defects in ctf1 and ctf18 mutants and that Ctf1p and Ctf18p physically interact with ORC, Cdt1p and MCM proteins. Furthermore, depletion of both Ctf1p and Ctf18p prevents S phase entry, retards S phase progression, and reduces pre-RC formation during the M-to-G1 transition. These data suggest that Ctf1p and Ctf18p together play important roles in regulating the initiation of DNA replication. © 2010 Landes Bioscience.-
dc.languageeng-
dc.relation.ispartofCell Cycle-
dc.subjectCTF18-
dc.subjectCTF1-
dc.subjectPlasmid loss-
dc.subjectPhenotypic screen-
dc.subjectBudding yeast-
dc.subjectDNA replication initiation-
dc.titleIdentification of novel factors involved in or regulating initiation of DNA replication by a genome-wide phenotypic screen in Saccharomyces cerevisiae-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.4161/cc.9.21.13679-
dc.identifier.scopuseid_2-s2.0-78349285501-
dc.identifier.volume9-
dc.identifier.issue21-
dc.identifier.spage4399-
dc.identifier.epage4410-
dc.identifier.eissn1551-4005-
dc.identifier.isiWOS:000283650500030-
dc.identifier.issnl1551-4005-

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