Low abundance of telomerase in yeast: Implications for telomerase haploinsufficiency

被引:101
作者
Mozdy, Amy D. [1 ]
Cech, Thomas R. [1 ]
机构
[1] Univ Colorado, Howard Hughes Med Inst, Dept Chem & Biochem, Boulder, CO 80309 USA
关键词
TLC1; telomerase; real-time PCR; telomere length regulation; haploinsufficiency;
D O I
10.1261/rna.134706
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
Telomerase is an RNA-dependent reverse transcriptase that maintains telomeric DNA at a species-specific equilibrium length. To determine an upper limit for the number of telomerase molecules in a Saccharomyces cerevisiae cell, we have established real-time RT-PCR assays to quantify the noncoding telomerase RNA, TLC1. We find that the number of TLC1 molecules in a haploid yeast cell is; 29, less than the number of chromosome ends ( 64) in late S-phase. Wild-type diploid cells contain; 37 telomerase RNAs, while diploids heterozygous for a null tlc1 allele have half the wild-type amount,; 19 TLC1 molecules. For comparison, there are; 480 molecules of the U2 snRNA per haploid cell. We show that a biological consequence of this low level of telomerase is haploinsufficiency: A TLC1/tlc1 Delta heterozygote maintains shorter telomeres. A dominant-negative telomerase RNA, with a deletion of the template for telomeric DNA synthesis, further demonstrates that yeast telomere length is sensitive to telomerase dosage. Sixfold overexpression of tlc1 Delta template establishes a new telomere length set point,; 160 bp shorter than wild type. Removing telomerase protein-interaction sites from the tlc1Dtemplate RNA mitigates the dominant-negative effect, suggesting that the tlc1Dtemplate RNA competes with wild-type TLC1 for a limited supply of telomerase proteins or for telomeres. Because yeast telomerase is tethered at chromosome ends, the finding that it may be outnumbered by its telomeric DNA substrates provides a new perspective for interpreting the results of telomere maintenance studies.
引用
收藏
页码:1721 / 1737
页数:17
相关论文
共 65 条
[1]   A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length [J].
Askree, SH ;
Yehuda, T ;
Smolikov, S ;
Gurevich, R ;
Hawk, J ;
Coker, C ;
Krauskopf, A ;
Kupiec, M ;
McEachern, MJM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (23) :8658-8663
[2]   Conserved N-terminal motifs of telomerase reverse transcriptase required for ribonucleoprotein assembly in vivo [J].
Bosoy, D ;
Peng, Y ;
Mian, IS ;
Lue, NF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :3882-3890
[3]  
Brachmann CB, 1998, YEAST, V14, P115
[4]  
Chapon C, 1997, RNA, V3, P1337
[5]   Structural elements required for association of the Saccharomyces cerevisiae telomerase RNA with the Est2 reverse transcriptase [J].
Chappell, AS ;
Lundblad, V .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (17) :7720-7736
[6]   Telomerase RNA structure and function: implications for dyskeratosis congenita [J].
Chen, JL ;
Greider, CW .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (04) :183-192
[7]   Telomere length homeostasis requires that telomerase levels are limiting [J].
Cristofari, G ;
Lingner, J .
EMBO JOURNAL, 2006, 25 (03) :565-574
[8]   A phylogenetically based secondary structure for the yeast telomerase RNA [J].
Dandjinou, AT ;
Lévesque, N ;
Larose, S ;
Lucier, JF ;
Elela, SA ;
Wellinger, RJ .
CURRENT BIOLOGY, 2004, 14 (13) :1148-1158
[9]  
de Lange T., 2006, TELOMERES
[10]   Mechanisms of haploinsufficiency revealed by genome-wide profiling in yeast [J].
Deutschbauer, AM ;
Jaramillo, DF ;
Proctor, M ;
Kumm, J ;
Hillenmeyer, ME ;
Davis, RW ;
Nislow, C ;
Giaever, G .
GENETICS, 2005, 169 (04) :1915-1925