(Q63383832)

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The proteasome is involved in determining differential utilization of double-strand break repair pathways

article by K Gudmundsdottir et al published 29 November 2007 in Oncogene

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The proteasome is involved in determining differential utilization of double-strand break repair pathways (English)

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3

A Ashworth

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Christopher J Lord

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2

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C J Lord

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K Gudmundsdottir

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1

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English

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publication date

11 June 2007

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29 November 2007

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published in

Oncogene

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volume

26

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issue

54

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page(s)

7601-7606

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7601-6

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.onc.1210579

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A system for stable expression of short interfering RNAs in mammalian cells

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Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

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Sem1, the yeast ortholog of a human BRCA2-binding protein, is a component of the proteasome regulatory particle that enhances proteasome stability

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DSS1 is required for RAD51 focus formation and genomic stability in mammalian cells

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Functional analysis of Rpn6p, a lid component of the 26 S proteasome, using temperature-sensitive rpn6 mutants of the yeast Saccharomyces cerevisiae

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Fission yeast Dss1 associates with the proteasome and is required for efficient ubiquitin-dependent proteolysis

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The BRCA2-Interacting Protein DSS1 Is Vital for DNA Repair, Recombination, and Genome Stability in Ustilago maydis

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Brh2-Dss1 interplay enables properly controlled recombination in Ustilago maydis

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Proteasome Involvement in the Repair of DNA Double-Strand Breaks

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DSS1 is required for the stability of BRCA2

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Interaction between the product of the breast cancer susceptibility gene BRCA2 and DSS1, a protein functionally conserved from yeast to mammals

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Rad23 links DNA repair to the ubiquitin/proteasome pathway

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Total synthesis of the potent proteasome inhibitor epoxomicin: a useful tool for understanding proteasome biology.

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Sem1p is a novel subunit of the 26 S proteasome from Saccharomyces cerevisiae

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Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences

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BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure

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Identifiers

DOI

10.1038/SJ.ONC.1210579

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1005921165

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17563742

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(Q63383832)

The proteasome is involved in determining differential utilization of double-strand break repair pathways

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