Literature DB >> 10975465

NFBD1/KIAA0170 is a novel nuclear transcriptional transactivator with BRCT domain.

T Ozaki1, T Nagase, S Ichimiya, N Seki, M Ohiri, N Nomura, N Takada, S Sakiyama, B L Weber, A Nakagawara.   

Abstract

The BRCT (BRCA1 C-terminus) superfamily includes a large number of nuclear proteins closely involved in DNA repair, recombination, and cell-cycle control. The human cDNA clone NFBD1 (previously designated KIAA0170) encodes a novel protein (2089 amino acids in length; calculated molecular mass 226,440 D) with possible BRCT domains at its carboxy terminus (amino acid residues 1894-2089). This gene product has been described as one of the BRCT superfamily proteins. However, its biological significance has been unclarified. Expression of green fluorescent protein (GFP)-tagged full-length NFBD1 or a series of deletion mutants indicated that NFBD1 was localized to the nucleus in various mammalian cells, and a 197-amino acid segment near the amino terminus (amino acid residues 142-338) contained a nuclear targeting signal. In vitro DNA-binding experiments showed that the highly basic region of NFBD1 (amino acid residues 1841-1893) possessed DNA-binding activity. The region encoding amino acids 508-995 of NFBD1 fused inframe with GAL4 DNA-binding domain activated transcription in both yeast and mammalian cells, while the possible BRCT domains of NFBD1 failed to induce transcription in mammalian cells. Overexpression of antisense NFBD1 RNA in a p53-deficient human osteogenic sarcoma cell line (SAOS-2) resulted in remarkable suppression of SAOS-2 colony formation. These results suggest that NFBD1 is a nuclear transcriptional transactivator with possible BRCT domains and may contribute to cell growth control.

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Year:  2000        PMID: 10975465     DOI: 10.1089/10445490050128403

Source DB:  PubMed          Journal:  DNA Cell Biol        ISSN: 1044-5498            Impact factor:   3.311


  18 in total

1.  Mutations in the TP53 gene affected recruitment of 53BP1 protein to DNA lesions, but level of 53BP1 was stable after γ-irradiation that depleted MDC1 protein in specific TP53 mutants.

Authors:  Jana Suchánková; Soňa Legartová; Eva Ručková; Bořivoj Vojtěšek; Stanislav Kozubek; Eva Bártová
Journal:  Histochem Cell Biol       Date:  2017-04-10       Impact factor: 4.304

2.  Growth inhibition, morphology change, and cell cycle alterations in NFBD1-depleted human esophageal cancer cells.

Authors:  Zhengmei Yang; Youquan Bu; Changdong Wang; Geli Liu; Fangzhou Song
Journal:  Mol Cell Biochem       Date:  2010-04-03       Impact factor: 3.396

3.  NFBD1/MDC1 participates in the regulation of proliferation and apoptosis in human laryngeal squamous cell carcinoma.

Authors:  X Liu; Z Qiu; Z Wang; W Zuo; Z Gong; C Liu; Q Zeng; Y Qian; L Jiang; Y Li; Y Bu; G Hu
Journal:  Clin Transl Oncol       Date:  2017-09-18       Impact factor: 3.405

4.  NFBD1/MDC1 is a protein of oncogenic potential in human cervical cancer.

Authors:  Chengfu Yuan; Youquan Bu; Changdong Wang; Faping Yi; Zhengmei Yang; Xiuning Huang; Li Cheng; Geli Liu; Yong Wang; Fangzhou Song
Journal:  Mol Cell Biochem       Date:  2011-08-19       Impact factor: 3.396

5.  NFBD1/MDC1 regulates Cav1 and Cav2 independently of DNA damage and p53.

Authors:  Kathleen A Wilson; Sierra A Colavito; Vincent Schulz; Patricia Heffernan Wakefield; William Sessa; David Tuck; David F Stern
Journal:  Mol Cancer Res       Date:  2011-05-06       Impact factor: 5.852

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

Authors:  Claudia Lukas; Fredrik Melander; Manuel Stucki; Jacob Falck; Simon Bekker-Jensen; Michal Goldberg; Yaniv Lerenthal; Stephen P Jackson; Jiri Bartek; Jiri Lukas
Journal:  EMBO J       Date:  2004-06-17       Impact factor: 11.598

7.  Knockdown of NFBD1/MDC1 enhances chemosensitivity to cisplatin or 5-fluorouracil in nasopharyngeal carcinoma CNE1 cells.

Authors:  Quan Zeng; Zhihai Wang; Chuan Liu; Zhitao Gong; Li Yang; Liang Jiang; Zuxia Ma; Yi Qian; Yucheng Yang; Houyong Kang; Suling Hong; Youquan Bu; Guohua Hu
Journal:  Mol Cell Biochem       Date:  2016-06-23       Impact factor: 3.396

8.  Mediator of DNA Damage Checkpoint 1 (MDC1) Is a Novel Estrogen Receptor Coregulator in Invasive Lobular Carcinoma of the Breast.

Authors:  Joseph L Sottnik; Evelyn K Bordeaux; Sanjana Mehrotra; Sarah E Ferrara; Andrew E Goodspeed; James C Costello; Matthew J Sikora
Journal:  Mol Cancer Res       Date:  2021-05-04       Impact factor: 5.852

Review 9.  p53: the attractive tumor suppressor in the cancer research field.

Authors:  Toshinori Ozaki; Akira Nakagawara
Journal:  J Biomed Biotechnol       Date:  2010-12-06

10.  Live Cell Imaging of Nuclear Actin Filaments and Heterochromatic Repair foci in Drosophila and Mouse Cells.

Authors:  Colby See; Deepak Arya; Emily Lin; Irene Chiolo
Journal:  Methods Mol Biol       Date:  2021
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