Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
about
Trypanosoma brucei BRCA2 acts in antigenic variation and has undergone a recent expansion in BRC repeat number that is important during homologous recombinationMolding BRCA2 function through its interacting partnersReplication protein A: directing traffic at the intersection of replication and repair.The breast cancer tumor suppressor BRCA2 promotes the specific targeting of RAD51 to single-stranded DNA.Schizosaccharomyces pombe Dss1p is a DNA damage checkpoint protein that recruits Rad24p, Cdc25p, and Rae1p to DNA double-strand breaks.DSSylation, a novel protein modification targets proteins induced by oxidative stress, and facilitates their degradation in cells.Structure and mechanism of action of the BRCA2 breast cancer tumor suppressorDual DNA-binding domains shape the interaction of Brh2 with DNA.Homologous recombination and its regulationD-loop formation by Brh2 protein of Ustilago maydis.Trypanosoma brucei BRCA2 acts in a life cycle-specific genome stability process and dictates BRC repeat number-dependent RAD51 subnuclear dynamics.Dss1 release activates DNA binding potential in Brh2DNA-binding Domain within the Brh2 N Terminus Is the Primary Interaction Site for Association with DNA.Ortholog of BRCA2-interacting protein BCCIP controls morphogenetic responses during DNA replication stress in Ustilago maydis.A cancer-associated BRCA2 mutation reveals masked nuclear export signals controlling localizationDss1 regulates interaction of Brh2 with DNA.DNA damage emergency: cellular garbage disposal to the rescue?BRCA2: one small step for DNA repair, one giant protein purified.Brh2 domain function distinguished by differential cellular responses to DNA damage and replication stress.The fungus Ustilago maydis and humans share disease-related proteins that are not found in Saccharomyces cerevisiae.Brh2 and Rad51 promote telomere maintenance in Ustilago maydis, a new model system of DNA repair proteins at telomeres.Mutational analysis of Brh2 reveals requirements for compensating mediator functions.Role of Blm and collaborating factors in recombination and survival following replication stress in Ustilago maydis.Identification of the deleted in split hand/split foot 1 protein as a novel biomarker for human cervical cancer.Dss1 Regulates Association of Brh2 with Rad51.Compensatory role for Rad52 during recombinational repair in Ustilago maydis.
P2860
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P2860
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
description
2007 nî lūn-bûn
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2007年の論文
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2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
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2007年论文
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2007年论文
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name
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
@ast
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
@en
type
label
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
@ast
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
@en
prefLabel
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
@ast
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
@en
P2093
P2860
P356
P1476
Dss1 interaction with Brh2 as a regulatory mechanism for recombinational repair
@en
P2093
Milorad Kojic
Nayef A Mazloum
Qingwen Zhou
William K Holloman
Zhimin Cao
P2860
P304
P356
10.1128/MCB.01907-06
P407
P577
2007-01-29T00:00:00Z