A self-regulating template in human telomerase

被引:25
作者
Brown, Andrew F. [1 ]
Podlevsky, Joshua D. [1 ]
Qi, Xiaodong [1 ]
Chen, Yinnan [1 ]
Xie, Mingyi [1 ]
Chen, Julian J. -L. [1 ]
机构
[1] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
基金
美国国家卫生研究院;
关键词
telomeres; ribonucleoprotein; polymerase; TETRAHYMENA TELOMERASE; RNA TEMPLATE; BOUNDARY DEFINITION; YEAST TELOMERASE; END-PROTECTION; SEQUENCE; VERTEBRATE; DETERMINES; EXPRESSION; MODEL;
D O I
10.1073/pnas.1402531111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Telomerase is a specialized reverse transcriptase (RT) containing an intrinsic telomerase RNA (TR) component. It synthesizes telomeric DNA repeats, (GGTTAG)n in humans, by reiteratively copying a precisely defined, short template sequence from the integral TR. The specific mechanism of how the telomerase active site uses this short template region accurately and efficiently during processive DNA repeat synthesis has remained elusive. Here we report that the human TR template, in addition to specifying the DNA sequence, is embedded with a single-nucleotide signal to pause DNA synthesis. After the addition of a dT residue to the DNA primer, which is specified by the 49 rA residue in the template, telomerase extends the DNA primer with three additional nucleotides and then pauses DNA synthesis. This sequence-defined pause site coincides precisely with the helix paired region 1 (P1)-defined physical template boundary and precludes the incorporation of nontelomeric nucleotides from residues outside the template region. Furthermore, this sequence-defined pausing mechanism is a key determinant, in addition to the P1-defined template boundary, for generating the characteristic 6-nt ladder banding pattern of telomeric DNA products in vitro. In the absence of the pausing signal, telomerase stalls nucleotide addition at multiple sites along the template, generating DNA products with heterogeneous terminal repeat registers. Our findings demonstrate that this unique self-regulating mechanism of the human TR template is essential for high-fidelity synthesis of DNA repeats.
引用
收藏
页码:11311 / 11316
页数:6
相关论文
共 30 条
[1]   BOUNDARY ELEMENTS OF THE TETRAHYMENA TELOMERASE RNA TEMPLATE AND ALIGNMENT DOMAINS [J].
AUTEXIER, C ;
GREIDER, CW .
GENES & DEVELOPMENT, 1995, 9 (18) :2227-2239
[2]   The RNA accordion model for template positioning by telomerase RNA during telomeric DNA synthesis [J].
Berman, Andrea J. ;
Akiyama, Benjamin M. ;
Stone, Michael D. ;
Cech, Thomas R. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2011, 18 (12) :1371-U84
[3]   Template boundary definition in mammalian telomerase [J].
Chen, JL ;
Greider, CW .
GENES & DEVELOPMENT, 2003, 17 (22) :2747-2752
[4]   Secondary structure of vertebrate telomerase RNA [J].
Chen, JL ;
Blasco, MA ;
Greider, CW .
CELL, 2000, 100 (05) :503-514
[5]   Human telomerase RNA accumulation in Cajal bodies facilitates telomerase recruitment to telomeres and telomere elongation [J].
Cristofari, Gael ;
Adolf, Emem ;
Reichenbach, Patrick ;
Sikora, Katarzyna ;
Terns, Rebecca M. ;
Terns, Michael P. ;
Lingner, Joachim .
MOLECULAR CELL, 2007, 27 (06) :882-889
[6]   Human telomerase RNA template sequence is a determinant of telomere repeat extension rate [J].
Drosopoulos, WC ;
DiRenzo, R ;
Prasad, VR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (38) :32801-32810
[7]   Multiple DNA-binding sites in Tetrahymena telomerase [J].
Finger, Sharon N. ;
Bryan, Tracy M. .
NUCLEIC ACIDS RESEARCH, 2008, 36 (04) :1260-1272
[8]   Yeast telomerase is specialized for C/A-rich RNA templates [J].
Förstemann, K ;
Zaug, AJ ;
Cech, TR ;
Lingner, J .
NUCLEIC ACIDS RESEARCH, 2003, 31 (06) :1646-1655
[9]   ALTERING SPECIFIC TELOMERASE RNA TEMPLATE RESIDUES AFFECTS ACTIVE-SITE FUNCTION [J].
GILLEY, D ;
LEE, MS ;
BLACKBURN, EH .
GENES & DEVELOPMENT, 1995, 9 (18) :2214-2226
[10]   Expression of mutant telomerase in immortal telomerase-negative human cells results in cell cycle deregulation, nuclear and chromosomal abnormalities and rapid loss of viability [J].
Guiducci, C ;
Cerone, MA ;
Bacchetti, S .
ONCOGENE, 2001, 20 (06) :714-725