Literature DB >> 9728393

Telomeres and double-strand breaks: trying to make ends meet.

A Bertuch1, V Lundblad.   

Abstract

Eukaryotic cells encounter two types of DNA ends: telomeres, the natural ends of linear chromosomes, and double-strand breaks, resulting from DNA damage or normal chromosomal processes such as meiotic or V(D)J recombination. These two termini have long been seen as functionally distinct, based on whether they are resistant to fusion with other ends or instead are acted upon by the DNA-repair machinery. However, a series of recent papers has shown that members of a set of proteins that are crucial for the rejoining of DNA strand breaks are also required for normal telomere function, raising new questions about how these two types of termini maintain their functional distinction.

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Year:  1998        PMID: 9728393     DOI: 10.1016/s0962-8924(98)01331-2

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  12 in total

1.  An anchorage nuclear structure for telomeric DNA repeats in HeLa cells.

Authors:  G Pierron; F Puvion-Dutilleul
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length.

Authors:  Syed H Askree; Tal Yehuda; Sarit Smolikov; Raya Gurevich; Joshua Hawk; Carrie Coker; Anat Krauskopf; Martin Kupiec; Michael J McEachern
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-25       Impact factor: 11.205

3.  Histone H3 and the histone acetyltransferase Hat1p contribute to DNA double-strand break repair.

Authors:  Song Qin; Mark R Parthun
Journal:  Mol Cell Biol       Date:  2002-12       Impact factor: 4.272

4.  DNA-binding and strand-annealing activities of human Mre11: implications for its roles in DNA double-strand break repair pathways.

Authors:  M de Jager; M L Dronkert; M Modesti; C E Beerens; R Kanaar; D C van Gent
Journal:  Nucleic Acids Res       Date:  2001-03-15       Impact factor: 16.971

5.  Ten1 functions in telomere end protection and length regulation in association with Stn1 and Cdc13.

Authors:  N Grandin; C Damon; M Charbonneau
Journal:  EMBO J       Date:  2001-03-01       Impact factor: 11.598

6.  Telomerase-dependent repeat divergence at the 3' ends of yeast telomeres.

Authors:  K Förstemann; M Höss; J Lingner
Journal:  Nucleic Acids Res       Date:  2000-07-15       Impact factor: 16.971

7.  Ku is associated with the telomere in mammals.

Authors:  H L Hsu; D Gilley; E H Blackburn; D J Chen
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-26       Impact factor: 11.205

8.  RAD50 function is essential for telomere maintenance in Arabidopsis.

Authors:  M E Gallego; C I White
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-13       Impact factor: 11.205

9.  Fission yeast Rhp51 is required for the maintenance of telomere structure in the absence of the Ku heterodimer.

Authors:  Tatsuya Kibe; Kazunori Tomita; Akira Matsuura; Daisuke Izawa; Tsutomu Kodaira; Takashi Ushimaru; Masahiro Uritani; Masaru Ueno
Journal:  Nucleic Acids Res       Date:  2003-09-01       Impact factor: 16.971

10.  Increased telomere length and hypersensitivity to DNA damaging agents in an Arabidopsis KU70 mutant.

Authors:  Paul Bundock; Haico van Attikum; Paul Hooykaas
Journal:  Nucleic Acids Res       Date:  2002-08-01       Impact factor: 16.971

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