Literature DB >> 9626966

A high yield of translocations parallels the high yield of sister chromatid exchanges in the CHO mutant EM9.

I Domínguez1, P Daza, A T Natarajan, F Cortés.   

Abstract

The fluorescence plus Giemsa (FPG) and fluorescence in situ hybridization (FISH) techniques have been used to determine, respectively, the frequencies of sister chromatid exchanges (SCEs) and stable chromosome aberrations (translocations) induced by different concentrations of BrdU in the Chinese hamster ovary cell mutant EM9 and its parental line AA8. The results indicate that BrdU induced a high frequency of SCEs and translocations in EM9 as compared with AA8, and that the translocation/dicentric ratio was also higher in the mutant cell line than in the parental cell line in both untreated and BrdU-treated cultures. These observations may indicate a possible relationship between the molecular mechanisms involved in the formation of SCEs and translocations.

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Year:  1998        PMID: 9626966     DOI: 10.1016/s0027-5107(97)00241-8

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  11 in total

1.  Double strand breaks (DSBs) as indicators of genomic instability in PATRR-mediated translocations.

Authors:  Sarah Correll-Tash; Brenna Lilley; Harold Salmons Iv; Elisabeth Mlynarski; Colleen P Franconi; Meghan McNamara; Carson Woodbury; Charles A Easley; Beverly S Emanuel
Journal:  Hum Mol Genet       Date:  2021-02-25       Impact factor: 6.150

Review 2.  H2O2-induced higher order chromatin degradation: a novel mechanism of oxidative genotoxicity.

Authors:  Gregory W Konat
Journal:  J Biosci       Date:  2003-02       Impact factor: 1.826

Review 3.  Coordination of DNA single strand break repair.

Authors:  Rachel Abbotts; David M Wilson
Journal:  Free Radic Biol Med       Date:  2016-11-24       Impact factor: 7.376

4.  The R280H X-ray cross-complementing 1 germline variant induces genomic instability and cellular transformation.

Authors:  Daria V Sizova; Agnes Keh; Ben F Taylor; Joann B Sweasy
Journal:  DNA Repair (Amst)       Date:  2015-05-14

5.  Quantitation of intracellular NAD(P)H can monitor an imbalance of DNA single strand break repair in base excision repair deficient cells in real time.

Authors:  Jun Nakamura; Shoji Asakura; Susan D Hester; Gilbert de Murcia; Keith W Caldecott; James A Swenberg
Journal:  Nucleic Acids Res       Date:  2003-09-01       Impact factor: 16.971

6.  Central role for the XRCC1 BRCT I domain in mammalian DNA single-strand break repair.

Authors:  Richard M Taylor; Angela Thistlethwaite; Keith W Caldecott
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

7.  JWA deficiency suppresses dimethylbenz[a]anthracene-phorbol ester induced skin papillomas via inactivation of MAPK pathway in mice.

Authors:  Zhenghua Gong; Yaowei Shi; Ze Zhu; Xuan Li; Yang Ye; Jianbing Zhang; Aiping Li; Gang Li; Jianwei Zhou
Journal:  PLoS One       Date:  2012-03-26       Impact factor: 3.240

8.  Translocation of XRCC1 and DNA ligase IIIalpha from centrosomes to chromosomes in response to DNA damage in mitotic human cells.

Authors:  Satoshi Okano; Li Lan; Alan E Tomkinson; Akira Yasui
Journal:  Nucleic Acids Res       Date:  2005-01-14       Impact factor: 16.971

9.  A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage.

Authors:  Sherif F El-Khamisy; Mitsuko Masutani; Hiroshi Suzuki; Keith W Caldecott
Journal:  Nucleic Acids Res       Date:  2003-10-01       Impact factor: 16.971

10.  JWA regulates XRCC1 and functions as a novel base excision repair protein in oxidative-stress-induced DNA single-strand breaks.

Authors:  Shouyu Wang; Zhenghua Gong; Rui Chen; Yunru Liu; Aiping Li; Gang Li; Jianwei Zhou
Journal:  Nucleic Acids Res       Date:  2009-02-10       Impact factor: 16.971

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