The FANCJ/MutLalpha interaction is required for correction of the cross-link response in FA-J cells (Q24312784)

1

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Rachel Litman

2

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Jenny Xie

3

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Sudha Sharma

4

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Robert M Brosh

5

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Sharon B Cantor

ATR kinase activation mediated by MutSalpha and MutLalpha in response to cytotoxic O6-methylguanine adducts

6

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language of work or name

English

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publication date

11 July 2007

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published in

The EMBO Journal

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volume

26

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issue

13

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page(s)

3238-49

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cites work

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The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations

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The BRCT Domain Is a Phospho-Protein Binding Domain

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N-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalpha

19 March 2017

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The mismatch repair system is required for S-phase checkpoint activation

19 March 2017

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BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function

19 March 2017

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BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures

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Immunoaffinity purification of mammalian protein complexes

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The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2

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Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

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Repair of DNA interstrand cross-links: interactions between homology-dependent and homology-independent pathways

7 April 2017

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Multifactorial contributions to an acute DNA damage response by BRCA1/BARD1-containing complexes

27 September 2017

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Signalling cell cycle arrest and cell death through the MMR System

27 September 2017

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BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ.

27 September 2017

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The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

27 September 2017

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The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair

27 September 2017

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A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients.

27 September 2017

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How Fanconi anemia proteins promote the four Rs: replication, recombination, repair, and recovery

27 September 2017

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ATR couples FANCD2 monoubiquitination to the DNA-damage response

27 September 2017

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Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

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DNA mismatch repair: molecular mechanisms and biological function

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Methylation-induced G2/M arrest requires a full complement of the mismatch repair protein hMLH1

27 September 2017

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Homologous repair of DNA damage and tumorigenesis: the BRCA connection

27 September 2017

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Defects in homologous recombination repair in mismatch-repair-deficient tumour cell lines

27 September 2017

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hMutSbeta is required for the recognition and uncoupling of psoralen interstrand cross-links in vitro

27 September 2017

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The 4N cell cycle delay in Fanconi anemia reflects growth arrest in late S phase

27 September 2017

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Arrest of S-phase progression is impaired in Fanconi anemia cells

27 September 2017

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Mismatch-, MutS-, MutL-, and helicase II-dependent unwinding from the single-strand break of an incised heteroduplex

27 September 2017

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MutS and MutL activate DNA helicase II in a mismatch-dependent manner

27 September 2017

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Evidence for a physical interaction between the Escherichia coli methyl-directed mismatch repair proteins MutL and UvrD.

27 September 2017

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DNA cross-linker-induced G2/M arrest in group C Fanconi anemia lymphoblasts reflects normal checkpoint function

27 September 2017

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Selective recognition of a cisplatin-DNA adduct by human mismatch repair proteins.

27 September 2017

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Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct

27 September 2017

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Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment

27 September 2017

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The effect of the Fanconi anemia polypeptide, FAC, upon p53 induction and G2 checkpoint regulation.

27 September 2017

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Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

27 September 2017

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Truncation of the C-terminus of human MLH1 blocks intracellular stabilization of PMS2 and disrupts DNA mismatch repair

29 November 2018

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The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

29 November 2018

1 reference

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Recovery from checkpoint-mediated arrest after repair of a double-strand break requires Srs2 helicase

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914102

Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system

29 November 2018

1 reference

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N-(2-chloroethyl)-N'-cyclohexyl-N-nitrosourea sensitivity in mismatch repair-defective human cells

29 November 2018

1 reference

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The cell cycle of lymphocytes in Fanconi anemia

29 November 2018

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12 December 2020

A simple diagnostic test for Fanconi anemia by flow cytometry

1 reference

12 December 2020

Sensitivity to DNA cross-linking chemotherapeutic agents in mismatch repair-defective cells in vitro and in xenografts

1 reference

12 December 2020

The MutL ATPase is required for mismatch repair

1 reference

12 December 2020

Unraveling the Fanconi anemia-DNA repair connection

1 reference

12 December 2020

Identifiers

DOI

10.1038/SJ.EMBOJ.7601754

1 reference

1 reference

1 reference

PubMed publication ID

17581638

1 reference