Analysis of telomerase in Candida albicans:: Potential role in telomere end protection

被引:31
作者
Singh, SM
Steinberg-Neifach, O
Mian, IS
Lue, NF
机构
[1] Cornell Univ, Weill Med Coll, WR Hearst Microbiol Res Ctr, Dept Microbiol & Immunol, New York, NY 10021 USA
[2] Lawrence Berkeley Natl Lab, Div Life Sci, Berkeley, CA 94720 USA
基金
英国惠康基金;
关键词
D O I
10.1128/EC.1.6.967-977.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Telomerase is a ribonucleoprotein reverse transcriptase responsible for the maintenance of one strand of telomere terminal repeats. Analysis of the telomerase complex in the budding yeast Saccharomyces cerevisiae has revealed the presence of one catalytic protein subunit (Est2p/TERT) and at least two noncatalytic components (Est1p and Est3p). The genome of the pathogenic yeast Candida albicans contains putative orthologues of all three, telomerase components. Disruption of each homologue resulted in significant but distinct telomere dysfunction in Candida. Similar to S. cerevisiae, the Candida EST3 disruption strain exhibits progressive telomere loss over many generations, at a rate that is consistent with incomplete replication. In contrast, telomeres in both the Candida TERT and EST1 disruption strains can contract rapidly, followed by partial or nearly complete recovery, suggesting a defect in telomere "capping." We propose that these two telomerase subunits may participate in the protection of chromosomal ends in Candida. Analysis of telomerase-mediated primer extension in vitro indicates that only the TERT protein is absolutely essential for enzyme activity. Our results support the conservation of telomerase protein components beyond the catalytic subunit but reveal species-specific phenotypic alterations in response to loss of individual telomerase component. We also identify potential homologues of Est1p in phylogenetically diverse organisms. The Est1p sequence family possesses a conserved N-terminal domain predicted to be structurally related to tetratricopeptide repeat-containing proteins.
引用
收藏
页码:967 / 977
页数:11
相关论文
共 61 条
[51]  
Qi HY, 2000, GENE DEV, V14, P1777
[52]   Saccharomyces cerevisiae telomerase is an Sm small nuclear ribonucleoprotein particle [J].
Seto, AG ;
Zaug, AJ ;
Sobel, SG ;
Wolin, SL ;
Cech, TR .
NATURE, 1999, 401 (6749) :177-180
[53]   Telomerase-independent lengthening of yeast telomeres occurs by an abrupt Rad50p-dependent, Rif-inhibited recombinational process [J].
Teng, SC ;
Chang, J ;
McCowan, B ;
Zakian, VA .
MOLECULAR CELL, 2000, 6 (04) :947-952
[54]   Template boundary in a yeast telomerase specified by RNA structure [J].
Tzfati, Y ;
Fulton, TB ;
Roy, J ;
Blackburn, EH .
SCIENCE, 2000, 288 (5467) :863-867
[55]   Est1 has the properties of a single-stranded telomere end-binding protein [J].
VirtaPearlman, V ;
Morris, DK ;
Lundblad, V .
GENES & DEVELOPMENT, 1996, 10 (24) :3094-3104
[56]  
WEINRICH SL, 1997, NAT GENET, V17, P198
[57]   Rapid hypothesis testing with Candida albicans through gene disruption with short homology regions [J].
Wilson, RB ;
Davis, D ;
Mitchell, AP .
JOURNAL OF BACTERIOLOGY, 1999, 181 (06) :1868-1874
[58]   Identification of functionally important domains in the N-terminal region of telomerase reverse transcriptase [J].
Xia, JQ ;
Peng, Y ;
Mian, IS ;
Lue, NF .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (14) :5196-5207
[59]   Telomere shortening and apoptosis in telomerase-inhibited human tumor cells [J].
Zhang, XL ;
Mar, V ;
Zhou, W ;
Harrington, L ;
Robinson, MO .
GENES & DEVELOPMENT, 1999, 13 (18) :2388-2399
[60]   The Est1 subunit of yeast telomerase binds the Tlc1 telomerase RNA [J].
Zhou, JL ;
Hidaka, K ;
Futcher, B .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (06) :1947-1955