Effects of double-strand break repair proteins on vertebrate telomere structure

被引:42
作者
Wei, C
Skopp, R
Takata, M
Takeda, S
Price, CM
机构
[1] Univ Cincinnati, Coll Med, Dept Mol Genet Biochem & Microbiol, Cincinnati, OH 45267 USA
[2] Univ Nebraska, Dept Vet Sci, Lincoln, NE 68588 USA
[3] Kawasaki Med Sch, Dept Immunol & Mol Genet, Okayama 7010192, Japan
[4] Kyoto Univ, Fac Med, Dept Radiat Genet, Kyoto 6068501, Japan
关键词
D O I
10.1093/nar/gkf396
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although telomeres are not recognized as double-strand breaks (DSBs), some DSB repair proteins are present at telomeres and are required for telomere maintenance. To learn more about the telomeric function of proteins from the homologous recombination (HR) and non-homologous end joining pathways (NHEJ), we have screened a panel of chicken DT40 knockout cell lines for changes in telomere structure. In contrast to what has been observed in Ku-deficient mice, we found that Ku70 disruption did not result in telomere-telomere fusions and had no effect on telomere length or the structure of the telomeric G-strand overhang. G-overhang length was increased by Rad51 disruption but unchanged by disruption of DNA-PKcs, Mre11, Rad52, Rad54, XRCC2 or XRCC3. The effect of Rad51 depletion was unexpected because gross alterations in telomere structure have not been detected in yeast HR mutants. Thus, our results indicate that Rad51 has a previously undiscovered function at vertebrate telomeres. They also indicate that Mre11 is not required to generate G-overhangs. Although Mre11 has been implicated in overhang generation, overhang structure had not previously been examined in Mre11-deficient cells. Overall our findings indicate that there are significant species-specific differences in the telomeric function of DSB repair proteins.
引用
收藏
页码:2862 / 2870
页数:9
相关论文
共 48 条
[21]   DNA double-strand breaks: signaling, repair and the cancer connection [J].
Khanna, KK ;
Jackson, SP .
NATURE GENETICS, 2001, 27 (03) :247-254
[22]   Cloning and characterisation of the chicken gene encoding the telomeric protein TRF2 [J].
Konrad, JP ;
Mills, W ;
Easty, DJ ;
Farr, CJ .
GENE, 1999, 239 (01) :81-90
[23]   Use of gene knockouts in cultured cells to study apoptosis [J].
Lahti, JM .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1999, 17 (04) :305-312
[24]   TELOMERE END-REPLICATION PROBLEM AND CELL AGING [J].
LEVY, MZ ;
ALLSOPP, RC ;
FUTCHER, AB ;
GREIDER, CW ;
HARLEY, CB .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 225 (04) :951-960
[25]  
Lewis LK, 2002, GENETICS, V160, P49
[26]   DNA ends: maintenance of chromosome termini versus repair of double strand breaks [J].
Lundblad, V .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2000, 451 (1-2) :227-240
[27]   The controlling role of ATM in homologous recombinational repair of DNA damage [J].
Morrison, C ;
Sonoda, E ;
Takao, N ;
Shinohara, A ;
Yamamoto, K ;
Takeda, S .
EMBO JOURNAL, 2000, 19 (03) :463-471
[28]   The telomerase reverse transcriptase: components and regulation [J].
Nugent, CI ;
Lundblad, V .
GENES & DEVELOPMENT, 1998, 12 (08) :1073-1085
[29]   Telomere maintenance is dependent on activities required for end repair of double-strand breaks [J].
Nugent, CI ;
Bosco, G ;
Ross, LO ;
Evans, SK ;
Salinger, AP ;
Moore, JK ;
Haber, JE ;
Lundblad, V .
CURRENT BIOLOGY, 1998, 8 (11) :657-660
[30]   Subsenescent telomere lengths in fibroblasts immortalized by limiting amounts of telomerase [J].
Ouellette, MM ;
Liao, M ;
Herbert, BS ;
Johnson, M ;
Holt, SE ;
Liss, HS ;
Shay, JW ;
Wright, WE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (14) :10072-10076