Literature DB >> 11118345

The BRCT regions of tumor suppressor BRCA1 and of XRCC1 show DNA end binding activity with a multimerizing feature.

K Yamane1, E Katayama, T Tsuruo.   

Abstract

The BRCT regions are two repeating structures in BRCA1 at the carboxyl-terminus and are ubiquitous in some proteins involved in cell cycle checkpoint and in DNA repair. Here, using electron microscopy, we show direct evidence that the BRCT regions of BRCA1 bound double-strand breaks of DNA. The BRCT regions could multimerize thus forming large protein particles. Smeared patterns of DNA fragments were consistently shown in the gel retardation assay. A single BRCT was sufficient for DNA binding. The smeared patterns were also observed in BRCTs of TopBP1, suggesting that multimerization may be an important feature of BRCTs. The recombinant second BRCT of XRCC1 (X-ray repair cross-complementing group 1), whose folding was determined by X-ray crystallography, also showed similar DNA end binding images. It is possible that some BRCTs are fundamental structures that detect DNA damages. Copyright 2000 Academic Press.

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Year:  2000        PMID: 11118345     DOI: 10.1006/bbrc.2000.3983

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  19 in total

1.  Phosphorylated BRCA1 is predominantly located in the nucleus and mitochondria.

Authors:  Elisabeth D Coene; Michael S Hollinshead; Anouk A T Waeytens; Vera R J Schelfhout; Willy P Eechaute; Michael K Shaw; Patrick M V Van Oostveldt; David J Vaux
Journal:  Mol Biol Cell       Date:  2004-12-09       Impact factor: 4.138

Review 2.  BRCT domains: easy as one, two, three.

Authors:  Charles Chung Yun Leung; J N Mark Glover
Journal:  Cell Cycle       Date:  2011-08-01       Impact factor: 4.534

3.  BRCA1 and BRCA2 mutations and treatment strategies for breast cancer.

Authors:  Inês Godet; Daniele M Gilkes
Journal:  Integr Cancer Sci Ther       Date:  2017-02-27

Review 4.  Two-way communications between ubiquitin-like modifiers and DNA.

Authors:  Helle D Ulrich
Journal:  Nat Struct Mol Biol       Date:  2014-04       Impact factor: 15.369

5.  Yeast DNA ligase IV mutations reveal a nonhomologous end joining function of BRCT1 distinct from XRCC4/Lif1 binding.

Authors:  Kishore K Chiruvella; Brian M Renard; Shanda R Birkeland; Sham Sunder; Zhuobin Liang; Thomas E Wilson
Journal:  DNA Repair (Amst)       Date:  2014-12

Review 6.  The structural basis of XRCC1-mediated DNA repair.

Authors:  Robert E London
Journal:  DNA Repair (Amst)       Date:  2015-02-16

7.  1H, 13C and 15N resonance assignments of the C-terminal BRCT domain from human BRCA1.

Authors:  Olaf J Gaiser; Hartmut Oschkinat; Udo Heinemann; Linda J Ball
Journal:  J Biomol NMR       Date:  2004-10       Impact factor: 2.835

8.  XRCC1 co-localizes and physically interacts with PCNA.

Authors:  Jinshui Fan; Marit Otterlei; Heng-Kuan Wong; Alan E Tomkinson; David M Wilson
Journal:  Nucleic Acids Res       Date:  2004-04-23       Impact factor: 16.971

9.  Site-directed mutagenesis analysis of the structural interaction of the single-strand-break repair protein, X-ray cross-complementing group 1, with DNA polymerase beta.

Authors:  Assen Marintchev; Michael R Gryk; Gregory P Mullen
Journal:  Nucleic Acids Res       Date:  2003-01-15       Impact factor: 16.971

10.  Human Rap1 interacts directly with telomeric DNA and regulates TRF2 localization at the telomere.

Authors:  N Özlem Arat; Jack D Griffith
Journal:  J Biol Chem       Date:  2012-10-20       Impact factor: 5.157

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