메뉴 건너뛰기




Volumn 208, Issue 12, 2015, Pages 621-624

Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure

Author keywords

Chromosomal instability; Colorectal cancer; DNA helicase MCM9; Hereditary mixed polyposis; Primary ovarian failure

Indexed keywords

CYTOSINE; GLUTAMIC ACID; GUANINE; LYSINE; MINICHROMOSOME MAINTENANCE PROTEIN 9; MCM9 PROTEIN, HUMAN; MINICHROMOSOME MAINTENANCE PROTEIN;

EID: 84949673296     PISSN: 22107762     EISSN: 22107770     Source Type: Journal    
DOI: 10.1016/j.cancergen.2015.10.001     Document Type: Article
Times cited : (52)

References (19)
  • 1
    • 84920470819 scopus 로고    scopus 로고
    • Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability
    • Al Asiri S., Basit S., Wood-Trageser M.A., et al. Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability. J Clin Invest 2015, 125:258-262.
    • (2015) J Clin Invest , vol.125 , pp. 258-262
    • Al Asiri, S.1    Basit, S.2    Wood-Trageser, M.A.3
  • 2
    • 84919620879 scopus 로고    scopus 로고
    • MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability
    • Wood-Trageser M.A., Gurbuz F., Yatsenko S.A., et al. MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability. Am J Hum Genet 2014, 95:754-762.
    • (2014) Am J Hum Genet , vol.95 , pp. 754-762
    • Wood-Trageser, M.A.1    Gurbuz, F.2    Yatsenko, S.A.3
  • 3
    • 47349113682 scopus 로고    scopus 로고
    • MCM9 binds Cdt1 and is required for the assembly of prereplication complexes
    • Lutzmann M., Mechali M. MCM9 binds Cdt1 and is required for the assembly of prereplication complexes. Mol Cell 2008, 31:190-200.
    • (2008) Mol Cell , vol.31 , pp. 190-200
    • Lutzmann, M.1    Mechali, M.2
  • 4
    • 84897513735 scopus 로고    scopus 로고
    • Molecular mechanisms of DNA replication checkpoint activation
    • Recolin B., van der Laan S., Tsanov N., et al. Molecular mechanisms of DNA replication checkpoint activation. Genes (Basel) 2014, 5:147-175.
    • (2014) Genes (Basel) , vol.5 , pp. 147-175
    • Recolin, B.1    van der Laan, S.2    Tsanov, N.3
  • 5
    • 34548277989 scopus 로고    scopus 로고
    • Genetic screen for chromosome instability in mice: Mcm4 and breast cancer
    • Shima N., Buske T.R., Schimenti J.C. Genetic screen for chromosome instability in mice: Mcm4 and breast cancer. Cell Cycle 2007, 6:1135-1140.
    • (2007) Cell Cycle , vol.6 , pp. 1135-1140
    • Shima, N.1    Buske, T.R.2    Schimenti, J.C.3
  • 6
    • 65949099311 scopus 로고    scopus 로고
    • How to load a replicative helicase onto chromatin: a more and more complex matter during evolution
    • Lutzmann M., Mechali M. How to load a replicative helicase onto chromatin: a more and more complex matter during evolution. Cell Cycle 2009, 8:1309-1313.
    • (2009) Cell Cycle , vol.8 , pp. 1309-1313
    • Lutzmann, M.1    Mechali, M.2
  • 7
    • 84865353862 scopus 로고    scopus 로고
    • Mcm8 and Mcm9 form a complex that functions in homologous recombination repair induced by DNA interstrand crosslinks
    • Nishimura K., Ishiai M., Horikawa K., et al. Mcm8 and Mcm9 form a complex that functions in homologous recombination repair induced by DNA interstrand crosslinks. Mol Cell 2012, 47:511-522.
    • (2012) Mol Cell , vol.47 , pp. 511-522
    • Nishimura, K.1    Ishiai, M.2    Horikawa, K.3
  • 8
    • 84876234845 scopus 로고    scopus 로고
    • The MCM8-MCM9 complex promotes RAD51 recruitment at DNA damage sites to facilitate homologous recombination
    • Park J., Long D.T., Lee K.Y., et al. The MCM8-MCM9 complex promotes RAD51 recruitment at DNA damage sites to facilitate homologous recombination. Mol Cell Biol 2013, 33:1632-1644.
    • (2013) Mol Cell Biol , vol.33 , pp. 1632-1644
    • Park, J.1    Long, D.T.2    Lee, K.Y.3
  • 9
    • 84940890030 scopus 로고    scopus 로고
    • MCM9 is required for mammalian DNA mismatch repair
    • Traver S., Coulombe P., Peiffer I., et al. MCM9 is required for mammalian DNA mismatch repair. Mol Cell 2015, 59:831-839.
    • (2015) Mol Cell , vol.59 , pp. 831-839
    • Traver, S.1    Coulombe, P.2    Peiffer, I.3
  • 10
    • 84896710456 scopus 로고    scopus 로고
    • Lynch syndrome in high risk Ashkenazi Jews in Israel
    • Goldberg Y., Kedar I., Kariiv R., et al. Lynch syndrome in high risk Ashkenazi Jews in Israel. Fam Cancer 2014, 13:65-73.
    • (2014) Fam Cancer , vol.13 , pp. 65-73
    • Goldberg, Y.1    Kedar, I.2    Kariiv, R.3
  • 11
    • 84861584357 scopus 로고    scopus 로고
    • Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1
    • Jaeger E., Leedham S., Lewis A., et al. Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1. Nat Genet 2012, 44:699-703.
    • (2012) Nat Genet , vol.44 , pp. 699-703
    • Jaeger, E.1    Leedham, S.2    Lewis, A.3
  • 12
    • 0034530575 scopus 로고    scopus 로고
    • Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer
    • Shiri-Sverdlov R., Oefner P., Green L., et al. Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer. Hum Mutat 2000, 16:491-501.
    • (2000) Hum Mutat , vol.16 , pp. 491-501
    • Shiri-Sverdlov, R.1    Oefner, P.2    Green, L.3
  • 13
    • 84883635842 scopus 로고    scopus 로고
    • Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility
    • Picelli S., Lorenzo Bermejo J., Chang-Claude J., et al. Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility. PLoS ONE 2013, 8:e72091.
    • (2013) PLoS ONE , vol.8 , pp. e72091
    • Picelli, S.1    Lorenzo Bermejo, J.2    Chang-Claude, J.3
  • 14
    • 84865396373 scopus 로고    scopus 로고
    • Unwinding to recombine
    • Guilbaud G., Sale J.E. Unwinding to recombine. Mol Cell 2012, 47:493-494.
    • (2012) Mol Cell , vol.47 , pp. 493-494
    • Guilbaud, G.1    Sale, J.E.2
  • 15
    • 0037440013 scopus 로고    scopus 로고
    • Identification and functional characterization of a new member of the human Mcm protein family: hMcm8
    • Gozuacik D., Chami M., Lagorce D., et al. Identification and functional characterization of a new member of the human Mcm protein family: hMcm8. Nucleic Acids Res 2003, 31:570-579.
    • (2003) Nucleic Acids Res , vol.31 , pp. 570-579
    • Gozuacik, D.1    Chami, M.2    Lagorce, D.3
  • 16
    • 80055085862 scopus 로고    scopus 로고
    • Minichromosome maintenance helicase paralog MCM9 is dispensible for DNA replication but functions in germ-line stem cells and tumor suppression
    • Hartford S.A., Luo Y., Southard T.L., et al. Minichromosome maintenance helicase paralog MCM9 is dispensible for DNA replication but functions in germ-line stem cells and tumor suppression. Proc Natl Acad Sci U S A 2011, 108:17702-17707.
    • (2011) Proc Natl Acad Sci U S A , vol.108 , pp. 17702-17707
    • Hartford, S.A.1    Luo, Y.2    Southard, T.L.3
  • 17
    • 84865368229 scopus 로고    scopus 로고
    • MCM8- and MCM9-deficient mice reveal gametogenesis defects and genome instability due to impaired homologous recombination
    • Lutzmann M., Grey C., Traver S., et al. MCM8- and MCM9-deficient mice reveal gametogenesis defects and genome instability due to impaired homologous recombination. Mol Cell 2012, 47:523-534.
    • (2012) Mol Cell , vol.47 , pp. 523-534
    • Lutzmann, M.1    Grey, C.2    Traver, S.3
  • 18
    • 84868617486 scopus 로고    scopus 로고
    • Cancer-associated variants and a common polymorphism of MUTYH exhibit reduced repair of oxidative DNA damage using a GFP-based assay in mammalian cells
    • Raetz A.G., Xie Y., Kundu S., et al. Cancer-associated variants and a common polymorphism of MUTYH exhibit reduced repair of oxidative DNA damage using a GFP-based assay in mammalian cells. Carcinogenesis 2012, 33:2301-2309.
    • (2012) Carcinogenesis , vol.33 , pp. 2301-2309
    • Raetz, A.G.1    Xie, Y.2    Kundu, S.3
  • 19
    • 0031052108 scopus 로고    scopus 로고
    • Bloom's syndrome. XX. The first 100 cancers
    • German J. Bloom's syndrome. XX. The first 100 cancers. Cancer Genet Cytogenet 1997, 93:100-106.
    • (1997) Cancer Genet Cytogenet , vol.93 , pp. 100-106
    • German, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.