Literature DB >> 9798685

Molecular cloning and chromosomal localization of Chinese hamster telomeric protein chTRF1. Its potential role in chromosomal instability.

L B Smilenov1, W Mellado, P H Rao, S G Sawant, C B Umbricht, S Sukumar, T K Pandita.   

Abstract

Chinese hamster cells frequently have altered karyotypes. To investigate the basis of recent observations that karyotypic alterations are related to telomeric fusions, we asked whether these alterations are due to lack of telomere repeat binding factor/s. Further, Chinese hamster chromosomes contain large blocks of interstitial telomeric repeats, which are preferentially involved in chromosome breakage and exchange, rendering it an interesting model for such studies. Here, we report on the cloning and the chromosomal localization of the Chinese hamster telomere repeat binding factor, chTRF1. The sequence analysis revealed, similar to human TRF1 (hTRF1), an N-terminal acidic domain, a TRF1 specific DNA binding motif and a C-terminal Myb type domain. Unlike mouse TRF1 (mTRF1), chTRF1 shows 97.5% identity to hTRF1. chTRF1 gene was localized on the long arm of chromosome 5. In vitro translation of chTRF1 resulted in protein product similar in molecular weight to hTRF1. Immunostaining of Chinese hamster ovary cells (CHO) with anti-TRF1 antibody revealed punctate nuclear staining. At metaphase, antibodies failed to detect TRF1 on most of the chromosome ends and the interstitial telomeric repeat bands. These studies suggest that chTRF1 does not bind the interstitial telomeric repeats, and its presence at the metaphase chromosome ends is limited. The later could be a factor contributing to frequent karyotypic alterations observed in Chinese hamster cells.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9798685     DOI: 10.1038/sj.onc.1202138

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  5 in total

1.  GSE4 peptide suppresses oxidative and telomere deficiencies in ataxia telangiectasia patient cells.

Authors:  Laura Pintado-Berninches; Beatriz Fernandez-Varas; Carlos Benitez-Buelga; Cristina Manguan-Garcia; Almudena Serrano-Benitez; Laura Iarriccio; Jaime Carrillo; Guillermo Guenechea; Susana P Egusquiaguirre; Jose-Luis Pedraz; Rosa M Hernández; Manoli Igartua; Elena G Arias-Salgado; Felipe Cortés-Ledesma; Leandro Sastre; Rosario Perona
Journal:  Cell Death Differ       Date:  2019-01-22       Impact factor: 15.828

2.  Involvement of human MOF in ATM function.

Authors:  Arun Gupta; Girdhar G Sharma; Charles S H Young; Manjula Agarwal; Edwin R Smith; Tanya T Paull; John C Lucchesi; Kum Kum Khanna; Thomas Ludwig; Tej K Pandita
Journal:  Mol Cell Biol       Date:  2005-06       Impact factor: 4.272

3.  Altered telomere nuclear matrix interactions and nucleosomal periodicity in ataxia telangiectasia cells before and after ionizing radiation treatment.

Authors:  L B Smilenov; S Dhar; T K Pandita
Journal:  Mol Cell Biol       Date:  1999-10       Impact factor: 4.272

4.  Atm inactivation results in aberrant telomere clustering during meiotic prophase.

Authors:  T K Pandita; C H Westphal; M Anger; S G Sawant; C R Geard; R K Pandita; H Scherthan
Journal:  Mol Cell Biol       Date:  1999-07       Impact factor: 4.272

5.  Human heterochromatin protein 1 isoforms HP1(Hsalpha) and HP1(Hsbeta) interfere with hTERT-telomere interactions and correlate with changes in cell growth and response to ionizing radiation.

Authors:  Girdhar G Sharma; Kyu-kye Hwang; Raj K Pandita; Arun Gupta; Sonu Dhar; Julie Parenteau; Manjula Agarwal; Howard J Worman; Raymund J Wellinger; Tej K Pandita
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.