Literature DB >> 9136882

XRCC1 protein interacts with one of two distinct forms of DNA ligase III.

R A Nash1, K W Caldecott, D E Barnes, T Lindahl.   

Abstract

Human DNA ligase III (103 kDa) has been shown to interact directly with the 70 kDa DNA repair protein, XRCC1. Here, the binding sites have been defined. Subcloned fragments of XRCC1 have been expressed and assayed for their ability to associate with DNA ligase III by far Western and affinity precipitation analyses. The C-terminal 96 amino acids of XRCC1 are necessary and sufficient for the specific interaction with DNA ligase III. A similar approach with the 103 kDa DNA ligase III has identified the C-terminal 148 amino acids of this enzyme as containing the binding site for XRCC1. An alternative 96 kDa form of DNA ligase III, abundant in testes, has been described [Chen, J., et al. (1995) Mol. Cell. Biol. 15, 5412-5422]. These two forms of DNA ligase III have identical N-terminal regions but differ toward their C termini and may be alternatively spliced products of the same gene. Antipeptide antibodies directed against the different C termini of the two forms of the enzyme indicate that both of them occur in vivo. The C-terminal region of the 96 kDa derivative of DNA ligase III is not able to interact with XRCC1. These findings indicate that only the larger form of DNA ligase III acts together with XRCC1, suggesting a role for this isoform of the enzyme in base excision repair.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9136882     DOI: 10.1021/bi962281m

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  84 in total

1.  An exonic splicing silencer in the testes-specific DNA ligase III beta exon.

Authors:  S L Chew; L Baginsky; I C Eperon
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

2.  Crystal structure of NAD(+)-dependent DNA ligase: modular architecture and functional implications.

Authors:  J Y Lee; C Chang; H K Song; J Moon; J K Yang; H K Kim; S T Kwon; S W Suh
Journal:  EMBO J       Date:  2000-03-01       Impact factor: 11.598

3.  A cell cycle-specific requirement for the XRCC1 BRCT II domain during mammalian DNA strand break repair.

Authors:  R M Taylor; D J Moore; J Whitehouse; P Johnson; K W Caldecott
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

4.  Mixed spermatogenic germ cell nuclear extracts exhibit high base excision repair activity.

Authors:  G W Intano; C A McMahan; R B Walter; J R McCarrey; C A Walter
Journal:  Nucleic Acids Res       Date:  2001-03-15       Impact factor: 16.971

5.  Phosphorylation and rapid relocalization of 53BP1 to nuclear foci upon DNA damage.

Authors:  L Anderson; C Henderson; Y Adachi
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

6.  Mutation of a BRCT domain selectively disrupts DNA single-strand break repair in noncycling Chinese hamster ovary cells.

Authors:  D J Moore; R M Taylor; P Clements; K W Caldecott
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

Review 7.  Structural and mechanistic conservation in DNA ligases.

Authors:  A J Doherty; S W Suh
Journal:  Nucleic Acids Res       Date:  2000-11-01       Impact factor: 16.971

8.  PTIP, a novel BRCT domain-containing protein interacts with Pax2 and is associated with active chromatin.

Authors:  M S Lechner; I Levitan; G R Dressler
Journal:  Nucleic Acids Res       Date:  2000-07-15       Impact factor: 16.971

9.  Disconnecting XRCC1 and DNA ligase III.

Authors:  Sachin Katyal; Peter J McKinnon
Journal:  Cell Cycle       Date:  2011-07-15       Impact factor: 4.534

10.  Human chromosomal translocations at CpG sites and a theoretical basis for their lineage and stage specificity.

Authors:  Albert G Tsai; Haihui Lu; Sathees C Raghavan; Markus Muschen; Chih-Lin Hsieh; Michael R Lieber
Journal:  Cell       Date:  2008-12-12       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.