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      분열형 효모에서의 mas2⁺ 유전자의 세포 내 기능

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      https://www.riss.kr/link?id=A76310137

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      국문 초록 (Abstract)

      유전자 발현의 조절은 세포주기 조절에 중요한 역할을 한다. 본 연구에서 새로운 mas2? (mitosis associated protein) 유전자는 인간의 SMARCAD1와 상동성을 갖고 분열형 효모인Schizosaccharomyces pombe (S. pombe)에서 gene-specific PCR방법에 의해서 분리하였다. 분리된 유전자는 SNF2 도메인이 위치해 있고, 이것은 염색체 재구성에 관련되어 있다. adh1?을 이용한 mas2? 전사체의 발현량 분석은 mas2?의 발현수준은 S. pombe에서 격막 형성 전에 가장 높았다. mas2? 완전돌연변이의 세포분열은 26와 35℃에서 지연되는 현상이 보였고, 다수의 다중 격막이나 핵분열이 일어나지 않는 세포들을 발견하였다. 세포들을 완전배지인 YES에서 증식을 증가시키기 위해서 배양했을 때, 정상과 다른 형태의 표현형을 가진 mas2? 완전돌연변이 세포들이 증가했다. 이런 표현형들은 mas2? 유전자의 과발현에 의해서 감소하였다. Mas2 단백질은 S. pombe의 핵내에 위치하였다. 이런 결과들은 mas2?가 인간의 SMARCAD1과 상동성을 갖고 있고, 염색체 재구성과 격막 형성 조절에 사용된다는 것을 나타낸다.
      번역하기

      유전자 발현의 조절은 세포주기 조절에 중요한 역할을 한다. 본 연구에서 새로운 mas2? (mitosis associated protein) 유전자는 인간의 SMARCAD1와 상동성을 갖고 분열형 효모인Schizosaccharomyces pombe (S. pomb...

      유전자 발현의 조절은 세포주기 조절에 중요한 역할을 한다. 본 연구에서 새로운 mas2? (mitosis associated protein) 유전자는 인간의 SMARCAD1와 상동성을 갖고 분열형 효모인Schizosaccharomyces pombe (S. pombe)에서 gene-specific PCR방법에 의해서 분리하였다. 분리된 유전자는 SNF2 도메인이 위치해 있고, 이것은 염색체 재구성에 관련되어 있다. adh1?을 이용한 mas2? 전사체의 발현량 분석은 mas2?의 발현수준은 S. pombe에서 격막 형성 전에 가장 높았다. mas2? 완전돌연변이의 세포분열은 26와 35℃에서 지연되는 현상이 보였고, 다수의 다중 격막이나 핵분열이 일어나지 않는 세포들을 발견하였다. 세포들을 완전배지인 YES에서 증식을 증가시키기 위해서 배양했을 때, 정상과 다른 형태의 표현형을 가진 mas2? 완전돌연변이 세포들이 증가했다. 이런 표현형들은 mas2? 유전자의 과발현에 의해서 감소하였다. Mas2 단백질은 S. pombe의 핵내에 위치하였다. 이런 결과들은 mas2?가 인간의 SMARCAD1과 상동성을 갖고 있고, 염색체 재구성과 격막 형성 조절에 사용된다는 것을 나타낸다.

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      다국어 초록 (Multilingual Abstract)

      The regulation of gene expression plays an important role in cell cycle controls. In this study, a novel mas2? (mitosis associated protein) gene, a homolog of human SMARCAD1 was isolated and characterized from a fission yeast Schizosaccharomyces pombe (S. pombe) using gene-specific polymerase chain reaction. The isolated gene contained a complete open reading frame capable of encoding 922 amino acid residues with a typical promoter, as judged by nucleotide sequence analysis. It was also found that an SNF2 domain is located, which is involved in the chromosome remodeling. The quantitative analysis of the mas2? transcript against adh1? showed that the expression level of mas2? is high before septum formation in S. pombe. When mas2? null mutant cells were grown at 27 and 35℃, the cytokinesis of mas2? null mutant was greatly delayed and a large number of multi-septate and mis-segregated cells were produced. In addition, the number of multi-septate cells significantly increased. When cells were cultured in YES rich medium to increase proliferation, the abnormal phenotypes mas2? null mutant dramatically increased. These phenotypes could be rescued by an overexpression of the mas2? gene. The Mas2 protein localized in the nuclei of S. pombe, as evidenced by Mas2-EGFP signals. These results suggest that the mas2? is homologous to human SMARCAD1 gene and involved in septum formation and chromosome remodeling control.
      번역하기

      The regulation of gene expression plays an important role in cell cycle controls. In this study, a novel mas2? (mitosis associated protein) gene, a homolog of human SMARCAD1 was isolated and characterized from a fission yeast Schizosaccharomyces pombe...

      The regulation of gene expression plays an important role in cell cycle controls. In this study, a novel mas2? (mitosis associated protein) gene, a homolog of human SMARCAD1 was isolated and characterized from a fission yeast Schizosaccharomyces pombe (S. pombe) using gene-specific polymerase chain reaction. The isolated gene contained a complete open reading frame capable of encoding 922 amino acid residues with a typical promoter, as judged by nucleotide sequence analysis. It was also found that an SNF2 domain is located, which is involved in the chromosome remodeling. The quantitative analysis of the mas2? transcript against adh1? showed that the expression level of mas2? is high before septum formation in S. pombe. When mas2? null mutant cells were grown at 27 and 35℃, the cytokinesis of mas2? null mutant was greatly delayed and a large number of multi-septate and mis-segregated cells were produced. In addition, the number of multi-septate cells significantly increased. When cells were cultured in YES rich medium to increase proliferation, the abnormal phenotypes mas2? null mutant dramatically increased. These phenotypes could be rescued by an overexpression of the mas2? gene. The Mas2 protein localized in the nuclei of S. pombe, as evidenced by Mas2-EGFP signals. These results suggest that the mas2? is homologous to human SMARCAD1 gene and involved in septum formation and chromosome remodeling control.

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      목차 (Table of Contents)

      • 서론
      • 재료 및 방법
      • 결과
      • 고찰
      • 요약
      • 서론
      • 재료 및 방법
      • 결과
      • 고찰
      • 요약
      • 감사의 글
      • References
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      참고문헌 (Reference)

      1 Nurse,P., "Universal control mechanism regulating onset of M-phase" 344 : 503-508, 1990

      2 Maundrell,K., "Thiamine-repressible expression vectors pREP and pRIP for fission yeast" 123 : 127-130, 1993

      3 Burns, L. G., "The yeast SWI-SNF complex facilitates binding of a transcriptional activator to nucleosomal sites in vivo" 17 : 4811-4819, 1997

      4 Laurent, B. C., "The yeast SNF2/SWI2 protein has DNA-stimulated ATPase activity required for transcriptional activation" 7 : 583-591, 1993

      5 Huang, S., "The premature ageing syndrome protein, WRN, is a 39 3 59 exonuclease" 20 : 114-116, 1998

      6 Kristen, E. N., "The complexity of chromatin remodeling and its links to cancer" 1603 : 19-29, 2002

      7 Peterson, C. L., "The SWI-SNF complex: a chromatin remodeling machine?" 20 : 143-146, 1995

      8 Deuring, R., "The ISWI chromatin-remodeling protein is required for gene expression and the maintenance of higher order chromatin structure in vivo" 5 : 355-365, 2000

      9 Auble, D. T., "Testing for DNA tracking by MOT1, a SNF2/SWI2 protein family member" 19 : 412-423, 1999

      10 Cote, J., "Stimulation of GAL4 derivative binding to nucleosomal DNA by the yeast SWI/SNF complex" 265 : 53-60, 1994

      1 Nurse,P., "Universal control mechanism regulating onset of M-phase" 344 : 503-508, 1990

      2 Maundrell,K., "Thiamine-repressible expression vectors pREP and pRIP for fission yeast" 123 : 127-130, 1993

      3 Burns, L. G., "The yeast SWI-SNF complex facilitates binding of a transcriptional activator to nucleosomal sites in vivo" 17 : 4811-4819, 1997

      4 Laurent, B. C., "The yeast SNF2/SWI2 protein has DNA-stimulated ATPase activity required for transcriptional activation" 7 : 583-591, 1993

      5 Huang, S., "The premature ageing syndrome protein, WRN, is a 39 3 59 exonuclease" 20 : 114-116, 1998

      6 Kristen, E. N., "The complexity of chromatin remodeling and its links to cancer" 1603 : 19-29, 2002

      7 Peterson, C. L., "The SWI-SNF complex: a chromatin remodeling machine?" 20 : 143-146, 1995

      8 Deuring, R., "The ISWI chromatin-remodeling protein is required for gene expression and the maintenance of higher order chromatin structure in vivo" 5 : 355-365, 2000

      9 Auble, D. T., "Testing for DNA tracking by MOT1, a SNF2/SWI2 protein family member" 19 : 412-423, 1999

      10 Cote, J., "Stimulation of GAL4 derivative binding to nucleosomal DNA by the yeast SWI/SNF complex" 265 : 53-60, 1994

      11 Du, J., "Sth1p, a Saccharomyces cerevisiae Snf2p/ Swi2p homolog, is an essential ATPase in RSC and differs from Snf/Swi in its interactions with histones and chromatin-associated proteins" 150 : 987-1005, 1998

      12 Schoor, M., "Skeletal dysplasias, growth retardation, reduced postnatal survival, and impaired fertility in mice lacking the SNF2/SWI2 family member ETL1" 85 : 73-83, 1999

      13 Utley, R. T., "SWI/SNF Stimulates the Formation of Disparate Activator-Nucleosome Complexes but Is Partially Redundant with Cooperative Binding" 272 : 12642-12649, 1997

      14 Gavin, I. J. H. Peter, "SWI/SNF Chromatin Remodeling Requires Changes in DNA Topology" 7 : 97-104, 2001

      15 Tom, O. H., "Persistent site-specific remodeling of a nucleosome array by transient action of the SWI/SNF complex" 273 : 513-516, 1996

      16 Gutz, H., "On homo- and heterothallism in Schizosaccharomyces pombe" 67 : 748-759, 1975

      17 Whitehouse, I., "Nucleosome mobilization catalysed by the yeast SWI/SNF complex" 400 : 784-787, 1999

      18 Coin, F., "Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH" 18 : 1357-1366, 1999

      19 Peterson,C.L., "Multiple switches to turn on chromatin?" 6 : 171-175, 1996

      20 Auble, D. T., "Mot1, a global repressor of RNA polymerase II transcription, inhibits TBP binding to DNA by an ATP-dependent mechanism" 8 : 1920-1934, 1994

      21 Auble, D. T., "Molecular analysis of the SNF2/SWI2 protein family member MOT1, an ATP-driven enzyme that dissociates TATA-binding protein from DNA" 17 : 4842-4851, 1997

      22 Lohman, T. M., "Mechanisms of helicase-catalyzed DNA unwinding" 65 : 169-214, 1996

      23 Ding, D. Q., "Large-scale screening of intracellular protein localization in living fission yeast cells by the use of a GFP-fusion genomic DNA library" 5 : 169-190, 2000

      24 Muchardt, C., "Human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor" 12 : 4279-4290, 1993

      25 Kanaar, R., "Human and mouse homologs of the Saccharomyces cerevisiae RAD54 DNA repair gene: evidence for functional conservation" 6 : 828-838, 1996

      26 Kohli, J, "Genetic Mapping in Schizosaccharomyces pombe by Mitotic and Meiotic Analysis and Induced Haploidization" 87 : 471-489, 1977

      27 Richmond, E., "Functional analysis of the DNA-stimulated ATPase domain of yeast SWI2/SNF2" 24 : 3685-3692, 1996

      28 Peterson, C. L., "Five SWI/SNF gene products are components of a large multisubunit complex required for transcriptional enhancement" 91 : 2905-2908, 1994

      29 Villard, L., "Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicase" 43 : 149-155, 1997

      30 West,S.C., "DNA helicases: New breeds of translocating motors and molecular pumps" 86 : 177-180, 1996

      31 Ellis,N.A., "DNA helicases in inherited human disorders" 7 : 354-363, 1997

      32 Varga-Weisz, P. D., "Chromatin-remodelling factor CHRAC contains the ATPases ISWI and topoisomerase II" 388 : 598-602, 1997

      33 Felsenfeld,G., "Chromatin unfolds" 86 : 13-19, 1996

      34 Fryer, C. J., "Chromatin remodelling by the glucocorticoid receptor requires the BRG1 complex" 393 : 88-91, 1998

      35 Workman, J. L., "Alteration of nucleosome structure as a mechanism of transcriptional regulation" 67 : 545-579, 1998

      36 Weeda, G., "A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy" 60 : 320-329, 1997

      37 Cairns, B. R., "A multisubunit complex containing the SWI1/ADR6, SWI2/SNF2, SWI3, SNF5, and SNF6 gene products isolated from yeast" 91 : 1950-1954, 1994

      38 Delmas, V., "A mammalian DNA-binding protein that contains a chromodomain and an SNF2/SWI2-like helicase domain" 90 : 2414-2418, 1993

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      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
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      2011-08-03 학술지명변경 외국어명 : Korean Journal of Life Science -> Journal of Life Science KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) 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
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.37 0.37 0.42
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.43 0.43 0.774 0.09
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