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      KCI등재 SCOPUS SCIE

      Phosphorylation of Mcm2 Protein by Cdc7 Kinase Is Not Essential for the Initiation of DNA Replication in Fission Yeast

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      https://www.riss.kr/link?id=A104429222

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      다국어 초록 (Multilingual Abstract)

      Previous studies in many species suggested that the minichromosome maintenance complex is a major physiological target of Cdc7. In this study, we examined the cellular role of Mcm2 phosphorylation by Cdc7 kinase in Schizosaccharomyces pombe. The in vi...

      Previous studies in many species suggested that the minichromosome maintenance complex
      is a major physiological target of Cdc7. In this study, we examined the cellular role of Mcm2
      phosphorylation by Cdc7 kinase in Schizosaccharomyces pombe. The in vitro phosphorylation
      of several truncated Mcm2 proteins by Cdc7 kinase showed that the major phosphorylation
      sites were located at N-terminus of Mcm2 protein. Alanine substitutions of several putative
      Cdc7 phosphorylation sites in this region resulted in the mutant Mcm2 proteins which were
      hardly phosphorylated by Cdc7 kinase in vitro. When these proteins were expressed in mcm2
      mutant cells, all of alanine substituted mutant proteins still complemented the temperature
      sensitive phenotype of mutant cells. These results suggest that the phosphorylation of Mcm2
      protein by Cdc7 kinase is not essential for the initiation of DNA replication. Cdc7 may play
      its essential roles by phosphorylating other Mcm subunits or proteins involved in the initiation
      of DNA replication.

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      다국어 초록 (Multilingual Abstract)

      Previous studies in many species suggested that the minichromosome maintenance complex is a major physiological target of Cdc7. In this study, we examined the cellular role of Mcm2 phosphorylation by Cdc7 kinase in Schizosaccharomyces pombe. The in ...

      Previous studies in many species suggested that the minichromosome maintenance complex
      is a major physiological target of Cdc7. In this study, we examined the cellular role of Mcm2
      phosphorylation by Cdc7 kinase in Schizosaccharomyces pombe. The in vitro phosphorylation
      of several truncated Mcm2 proteins by Cdc7 kinase showed that the major phosphorylation
      sites were located at N-terminus of Mcm2 protein. Alanine substitutions of several putative
      Cdc7 phosphorylation sites in this region resulted in the mutant Mcm2 proteins which were
      hardly phosphorylated by Cdc7 kinase in vitro. When these proteins were expressed in mcm2
      mutant cells, all of alanine substituted mutant proteins still complemented the temperature
      sensitive phenotype of mutant cells. These results suggest that the phosphorylation of Mcm2
      protein by Cdc7 kinase is not essential for the initiation of DNA replication. Cdc7 may play
      its essential roles by phosphorylating other Mcm subunits or proteins involved in the initiation
      of DNA replication.

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      참고문헌 (Reference)

      1 Hardy CF, "mcm5/cdc46-bob1 bypasses the requirement for the S phase activator Cdc7p" 94 : 3151-3155, 1997

      2 Labib K, "Uninterrupted MCM2-7 function required for DNA replication fork progression" 288 : 1643-1647, 2000

      3 Lee JK, "The Cdc23 (Mcm10) protein is required for the phosphorylation of minichromosome maintenance complex by the Dfp1-Hsk1 kinase" 100 : 2334-2339, 2003

      4 Blow JJ, "Preventing re-replication of chromosomal DNA" 6 : 476-486, 2005

      5 Masai H, "Phosphorylation of Mcm4 by Cdc7 kinase facilitates its interaction with Cdc45 on the chromatin" 281 : 39249-39261, 2006

      6 Mendez J, "Perpetuating the double helix: molecular machines at eukaryotic DNA replication origins" 25 : 1158-1167, 2003

      7 Lei M, "Mcm2 is a target of regulation by Cdc7-Dbf4 during the initiation of DNA synthesis" 11 : 3365-3374, 1997

      8 Tye BK, "MCM proteins in DNA replication" 68 : 649-686, 1999

      9 Montagnoli A, "Identification of Mcm2 phosphorylation sites by S-phase-regulating kinases" 281 : 10281-10290, 2006

      10 Sato N, "Human and Xenopus cDNAs encoding budding yeast Cdc7-related kinases: in vitro phosphorylation of Mcm subunits by a putative human homologue of Cdc7" 16 : 4340-4351, 1997

      1 Hardy CF, "mcm5/cdc46-bob1 bypasses the requirement for the S phase activator Cdc7p" 94 : 3151-3155, 1997

      2 Labib K, "Uninterrupted MCM2-7 function required for DNA replication fork progression" 288 : 1643-1647, 2000

      3 Lee JK, "The Cdc23 (Mcm10) protein is required for the phosphorylation of minichromosome maintenance complex by the Dfp1-Hsk1 kinase" 100 : 2334-2339, 2003

      4 Blow JJ, "Preventing re-replication of chromosomal DNA" 6 : 476-486, 2005

      5 Masai H, "Phosphorylation of Mcm4 by Cdc7 kinase facilitates its interaction with Cdc45 on the chromatin" 281 : 39249-39261, 2006

      6 Mendez J, "Perpetuating the double helix: molecular machines at eukaryotic DNA replication origins" 25 : 1158-1167, 2003

      7 Lei M, "Mcm2 is a target of regulation by Cdc7-Dbf4 during the initiation of DNA synthesis" 11 : 3365-3374, 1997

      8 Tye BK, "MCM proteins in DNA replication" 68 : 649-686, 1999

      9 Montagnoli A, "Identification of Mcm2 phosphorylation sites by S-phase-regulating kinases" 281 : 10281-10290, 2006

      10 Sato N, "Human and Xenopus cDNAs encoding budding yeast Cdc7-related kinases: in vitro phosphorylation of Mcm subunits by a putative human homologue of Cdc7" 16 : 4340-4351, 1997

      11 Masai H, "Human Cdc7-related kinase complex. In vitro phosphorylation of Mcm by concerted actions of Cdks and Cdc7 and that of a criticial threonine residue of Cdc7 bY Cdks" 275 : 29042-29052, 2000

      12 Gambus A, "GINS maintains association of Cdc45 with MCM in replisome progression complexes at eukaryotic DNA replication forks" 8 : 358-366, 2006

      13 Forsburg SL, "Eukaryotic MCM proteins: beyond replication initiation" 68 : 109-131, 2004

      14 Tsuji T, "Essential role of phosphorylation of Mcm2 by Cdc7/Dbf4 in the initiation of DNA replication in mammalian cells" 17 : 4459-4472, 2006

      15 Ferreira MF, "Dbf4p, an essential S phase-promoting factor, is targeted for degradation by the anaphase-promoting complex" 20 : 242-248, 2000

      16 Bell SP, "DNA replication in eukaryotic cells" 71 : 333-374, 2002

      17 Kihara M, "Characterization of the yeast Cdc7p/Dbf4p complex purified from insect cells. Its protein kinase activity is regulated by Rad53p" 275 : 35051-35062, 2000

      18 Oshiro G, "Cell cycle control of Cdc7p kinase activity through regulation of Dbf4p stability" 19 : 4888-4896, 1999

      19 Sheu YJ, "Cdc7-Dbf4 phosphorylates Mcm proteins via a docking site-mediated mechanism to promote S phase progression" 24 : 101-113, 2006

      20 Donaldson AD, "Cdc7 is required throughout the yeast S phase to activate replication origins" 12 : 491-501, 1998

      21 Aparicio T, "Cdc45-MCM- GINS, a new power player for DNA replication" 1 : 18-, 2006

      22 Cho WH, "CDC7 kinase phosphorylates serine residues adjacent to acidic amino acids in the minichromosome maintenance 2 protein" 103 : 11521-11526, 2006

      23 Ishimi Y, "Biochemical activities associated with mouse Mcm2 protein" 276 : 42744-42752, 2001

      24 Bell SP, "ATP-dependent recognition of eukaryotic origins of DNA replication by a multiprotein complex" 357 : 128-134, 1992

      25 Ishimi Y, "A DNA helicase activity is associated with an Mcm 4, -6, and -7 protein complex" 272 : 24508-24513, 1997

      26 Johnston LH, "A Cdc7p-Dbf4p protein kinase activity is conserved from yeast to humans" 4 : 61-69, 2000

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2012-05-07 학술지명변경 한글명 : 한국유전학회지 -> Genes & Genomics KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-04-14 학술지명변경 외국어명 : Korean Journal of Genetics -> Genes and Genomics KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.51 0.12 0.38
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.32 0.27 0.258 0.02
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