Identification of TTAGGG-binding proteins in Neurospora crassa, a fungus with vertebrate-like telomere repeats

被引:14
作者
Casas-Vila, Nuria [1 ]
Scheibe, Marion [1 ]
Freiwald, Anja [1 ]
Kappei, Dennis [2 ]
Butter, Falk [1 ]
机构
[1] Inst Mol Biol IMB gGmbH, Quantitat Prote, D-55128 Mainz, Germany
[2] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore 117599, Singapore
基金
新加坡国家研究基金会;
关键词
Interactomics; Mass spectrometry; Telomere; Telosome; Evolution; SACCHAROMYCES-CEREVISIAE; TAY1; PROTEIN; IN-VITRO; YEAST; DNA; CHROMATIN; LENGTH; END; QUANTIFICATION; PURIFICATION;
D O I
10.1186/s12864-015-2158-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: To date, telomere research in fungi has mainly focused on Saccharomyces cerevisiae and Schizosaccharomyces pombe, despite the fact that both yeasts have degenerated telomeric repeats in contrast to the canonical TTAGGG motif found in vertebrates and also several other fungi. Results: Using label-free quantitative proteomics, we here investigate the telosome of Neurospora crassa, a fungus with canonical telomeric repeats. We show that at least six of the candidates detected in our screen are direct TTAGGG-repeat binding proteins. While three of the direct interactors (NCU03416 [ncTbf1], NCU01991 [ncTbf2] and NCU02182 [ncTay1]) feature the known myb/homeobox DNA interaction domain also found in the vertebrate telomeric factors, we additionally show that a zinc-finger protein (NCU07846) and two proteins without any annotated DNA-binding domain (NCU02644 and NCU05718) are also direct double-strand TTAGGG binders. We further find two single-strand binders (NCU02404 [ncGbp2] and NCU07735 [ncTcg1]). Conclusion: By quantitative label-free interactomics we identify TTAGGG-binding proteins in Neurospora crassa, suggesting candidates for telomeric factors that are supported by phylogenomic comparison with yeast species. Intriguingly, homologs in yeast species with degenerated telomeric repeats are also TTAGGG-binding proteins, e.g. in S. cerevisiae Tbf1 recognizes the TTAGGG motif found in its subtelomeres. However, there is also a subset of proteins that is not conserved. While a rudimentary core TTAGGG-recognition machinery may be conserved across yeast species, our data suggests Neurospora as an emerging model organism with unique features.
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页数:9
相关论文
共 34 条
[1]  
[Anonymous], CIBA FDN S
[2]   Telomeric RNA-DNA hybrids affect telomere-length dynamics and senescence [J].
Balk, Bettina ;
Maicher, Andre ;
Dees, Martina ;
Klermund, Julia ;
Luke-Glaser, Sarah ;
Bender, Katharina ;
Luke, Brian .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2013, 20 (10) :1199-+
[3]   Isolation of Chromatin from Dysfunctional Telomeres Reveals an Important Role for Ring1b in NHEJ-Mediated Chromosome Fusions [J].
Bartocci, Cristina ;
Diedrich, Jolene K. ;
Ouzounov, Iliana ;
Li, Julia ;
Piunti, Andrea ;
Pasini, Diego ;
Yates, John R., III ;
Denchi, Eros Lazzerini .
CELL REPORTS, 2014, 7 (04) :1320-1332
[4]   Subtelomeric proteins negatively regulate telomere elongation in budding yeast [J].
Berthiau, AS ;
Yankulov, K ;
Bah, A ;
Revardel, E ;
Luciano, P ;
Wellinger, RJ ;
Géli, V ;
Gilson, E .
EMBO JOURNAL, 2006, 25 (04) :846-856
[5]   Tbf1 and Vid22 promote resection and non-homologous end joining of DNA double-strand break ends [J].
Bonetti, Diego ;
Anbalagan, Savani ;
Lucchini, Giovanna ;
Clerici, Michela ;
Longhese, Maria Pia .
EMBO JOURNAL, 2013, 32 (02) :275-289
[6]   AN ESSENTIAL YEAST GENE ENCODING A TTAGGG REPEAT-BINDING PROTEIN [J].
BRIGATI, C ;
KURTZ, S ;
BALDERES, D ;
VIDALI, G ;
SHORE, D .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (02) :1306-1314
[7]   A YEAST PROTEIN THAT INFLUENCES THE CHROMATIN STRUCTURE OF UASG AND FUNCTIONS AS A POWERFUL AUXILIARY GENE ACTIVATOR [J].
CHASMAN, DI ;
LUE, NF ;
BUCHMAN, AR ;
LAPOINTE, JW ;
LORCH, Y ;
KORNBERG, RD .
GENES & DEVELOPMENT, 1990, 4 (04) :503-514
[8]   A HUMAN TELOMERIC PROTEIN [J].
CHONG, L ;
VANSTEENSEL, B ;
BROCCOLI, D ;
ERDJUMENTBROMAGE, H ;
HANISH, J ;
TEMPST, P ;
DELANGE, T .
SCIENCE, 1995, 270 (5242) :1663-1667
[9]   Regulation of telomere length and function by a Myb-domain protein in fission yeast [J].
Cooper, JP ;
Nimmo, ER ;
Allshire, RC ;
Cech, TR .
NATURE, 1997, 385 (6618) :744-747
[10]   How the human telomeric proteins TRF1 and TRF2 recognize telomeric DNA: a view from high-resolution crystal structures [J].
Court, R ;
Chapman, L ;
Fairall, L ;
Rhodes, D .
EMBO REPORTS, 2005, 6 (01) :39-45