Literature DB >> 12499369

NFBD1/KIAA0170 is a chromatin-associated protein involved in DNA damage signaling pathways.

Xingzhi Xu1, David F Stern.   

Abstract

NFBD1/KIAA0170 is a nuclear factor with an N-terminal FHA (forkhead-associated) domain and a tandem repeat of BRCT (breast cancer susceptibility gene-1 C terminus) domains, both of which are present in a number of proteins involved in DNA repair and/or DNA damage signaling pathways. We have investigated the association of NFBD1 with DNA damage responses. We found that the NFBD1 transcript is abundant in the testis relative to other tissues. NFBD1 is a chromatin-associated protein and is modified in G(2)/M phase or after DNA damage. NFBD1 phosphorylation in response to ionizing radiation (IR) was ATM-dependent. NFBD1 exhibited diffuse nuclear staining in the majority of untreated cells analyzed by indirect immunofluorescence and formed discrete nuclear foci after exposure to IR, UV radiation, and hydroxyurea treatment. IR induced NFBD1 foci within 1 min. The foci colocalized with gamma-H2AX foci, which have been previously shown to localize at sites of DNA double-strand breaks. IR-induced NFBD1 foci also colocalized with 53BP1 and MRE11/RAD50 foci. Taken together, these results suggest that NFBD1 is a mediator of DNA damage-dependent signaling.

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Year:  2002        PMID: 12499369     DOI: 10.1074/jbc.M211392200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  40 in total

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2.  Differential regulation of centrosome integrity by DNA damage response proteins.

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3.  Interplay between the DNA damage proteins MDC1 and ATM in the regulation of the spindle assembly checkpoint.

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Journal:  J Biol Chem       Date:  2014-02-07       Impact factor: 5.157

4.  RNF126 as a Biomarker of a Poor Prognosis in Invasive Breast Cancer and CHEK1 Inhibitor Efficacy in Breast Cancer Cells.

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Review 5.  BRCA1 and its toolbox for the maintenance of genome integrity.

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6.  DNA damage signaling in response to double-strand breaks during mitosis.

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7.  Rad53 phosphorylation site clusters are important for Rad53 regulation and signaling.

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Journal:  Mol Cell Biol       Date:  2003-09       Impact factor: 4.272

8.  Mdc1 couples DNA double-strand break recognition by Nbs1 with its H2AX-dependent chromatin retention.

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Review 9.  Assembly of checkpoint and repair machineries at DNA damage sites.

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10.  Histone H2A phosphorylation controls Crb2 recruitment at DNA breaks, maintains checkpoint arrest, and influences DNA repair in fission yeast.

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