Mrc1 protects uncapped budding yeast telomeres from exonuclease EXO1

被引:20
作者
Tsolou, Avgi [1 ]
Lydall, David [1 ]
机构
[1] Newcastle Univ, Ctr Integrated Syst Biol Ageing & Nutr, Inst Ageing & Hlth, Henry Wellcome Lab Biogerontol Res, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
基金
英国惠康基金;
关键词
Mrc1; telomere; ssDNA; CDC13; YKU70; EXO1;
D O I
10.1016/j.dnarep.2007.05.010
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mrc1 (Mediator of Replication Checkpoint 1) is a component of the DNA replication fork machinery and is necessary for checkpoint activation after replication stress. in this study, we addressed the role of Mrc1 at uncapped telomeres. Our experiments show that Mrc1 contributes to the vitality of both cdc13-1 and yku70 Delta telomere capping mutants. Cells with telomere capping defects containing MRC1 or mrc1(AQ), a checkpoint defective allele, exhibit similar growth, suggesting growth defects of cdc13-1 mrc1 Delta are not due to checkpoint defects. This is in accordance with Mrc1-independent Rad53 activation after telomere uncapping. Poor growth of cdc13-1 mutants in the absence of Mrc1 is a result of enhanced single stranded DNA accumulation at uncapped telomeres. Consistent with this, deletion of EXO1, encoding a nuclease that contributes to single stranded DNA accumulation after telomere uncapping, improves growth of cdc13-1 mrc1 Delta strains and decreases ssDNA production. Our observations show that Mrc1, a core component of the replication fork, plays an important role in telomere capping, protecting from nucleases and checkpoint pathways. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1607 / 1617
页数:11
相关论文
共 60 条
[1]  
Adams A., 1997, METHODS YEAST GENETI
[2]  
Adams AK, 1996, MOL CELL BIOL, V16, P4614
[3]   Mrc1 transduces signals of DNA replication stress to activate Rad53 [J].
Alcasabas, AA ;
Osborn, AJ ;
Bachant, J ;
Hu, FH ;
Werler, PJH ;
Bousset, K ;
Furuya, K ;
Diffley, JFX ;
Carr, AM ;
Elledge, SJ .
NATURE CELL BIOLOGY, 2001, 3 (11) :958-965
[4]   Switching and signaling at the telomere [J].
Blackburn, EH .
CELL, 2001, 106 (06) :661-673
[5]   A domain of Rad9 specifically required for activation of Chk1 in budding yeast [J].
Blankley, RT ;
Lydall, D .
JOURNAL OF CELL SCIENCE, 2004, 117 (04) :601-608
[6]   Quantitative amplification of single-stranded DNA (QAOS) demonstrates that cdc13-1 mutants generate ssDNA in a telomere to centromere direction [J].
Booth, C ;
Griffith, E ;
Brady, G ;
Lydall, D .
NUCLEIC ACIDS RESEARCH, 2001, 29 (21) :4414-4422
[7]   Molecular anatomy and regulation of a stable replisome eukaryotic DNA at a paused replication fork [J].
Calzada, A ;
Hodgson, B ;
Kanemaki, M ;
Bueno, A ;
Labib, K .
GENES & DEVELOPMENT, 2005, 19 (16) :1905-1919
[8]   CDC17 - AN ESSENTIAL GENE THAT PREVENTS TELOMERE ELONGATION IN YEAST [J].
CARSON, MJ ;
HARTWELL, L .
CELL, 1985, 42 (01) :249-257
[9]   Yeast Sml1, a protein inhibitor of ribonucleotide reductase [J].
Chabes, A ;
Domkin, V ;
Thelander, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36679-36683
[10]   ONE-STEP TRANSFORMATION OF YEAST IN STATIONARY PHASE [J].
CHEN, DC ;
YANG, BC ;
KUO, TT .
CURRENT GENETICS, 1992, 21 (01) :83-84