Regulation of murine telomere length by Rtel:: An essential gene encoding a helicase-like protein

被引:259
作者
Ding, H
Schertzer, M
Wu, XL
Gertsenstein, M
Selig, S
Kammori, M
Pourvali, R
Poon, S
Vulto, I
Chavez, E
Tam, PPL
Nagy, A
Lansdorp, PM [1 ]
机构
[1] British Columbia Canc Agcy, Terry Fox Lab, Vancouver, BC V5Z 1L3, Canada
[2] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[3] Univ Sydney, Childrens Med Res Inst, Embryol Unit, Westmead, NSW 2145, Australia
[4] Rambam Med Ctr, IL-31096 Haifa, Israel
[5] Technion Israel Inst Technol, Fac Med, IL-31096 Haifa, Israel
[6] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
[7] Univ British Columbia, Dept Med, Vancouver, BC V5Z 4E3, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.cell.2004.05.026
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
Little is known about the genes that regulate telomere length diversity between mammalian species. A candidate gene locus was previously mapped to a region on distal mouse Chr 2q. Within this region, we identified a gene similar to the dog-1 DNA helicase-like gene in C. elegans. We cloned this Regulator of telomere length (Rtel) gene and inactivated its expression in mice. Rtel(-/-) mice died between days 10 and 11.5 of gestation with defects in the nervous system, heart, vasculature, and extraembryonic tissues. Rtel(-/-) embryonic stem cells showed telomere loss and displayed many chromosome breaks and fusions upon differentiation in vitro. Crosses of Rtel(+/-) mice with Mus spretus showed that Rtel from the Mus musculus parent is required for telomere elongation of M. spretus chromosomes in F1 cells. We conclude that Rtel is an essential gene that regulates telomere length and prevents genetic instability.
引用
收藏
页码:873 / 886
页数:14
相关论文
共 55 条
  • [1] ES cells do not activate p53-dependent stress responses and undergo p53-independent apoptosis in response to DNA damage
    Aladjem, MI
    Spike, BT
    Rodewald, LW
    Hope, TJ
    Klemm, M
    Jaenisch, R
    Wahl, GM
    [J]. CURRENT BIOLOGY, 1998, 8 (03) : 145 - 155
  • [2] mTert expression correlates with telomerase activity during the differentiation of murine embryonic stem cells
    Armstrong, L
    Lako, M
    Lincoln, J
    Cairns, PM
    Hole, N
    [J]. MECHANISMS OF DEVELOPMENT, 2000, 97 (1-2) : 109 - 116
  • [3] Telomere length measurements in leukocyte subsets by automated multicolor flow-FISH
    Baerlocher, GM
    Lansdorp, PM
    [J]. CYTOMETRY PART A, 2003, 55A (01): : 1 - 6
  • [4] Overexpression of M68/DcR3 in human gastrointestinal tract tumors independent of gene amplification and its location in a four-gene cluster
    Bai, C
    Connolly, B
    Metzker, ML
    Hilliard, CA
    Liu, XM
    Sandig, V
    Soderman, A
    Galloway, SM
    Liu, QY
    Austin, CP
    Caskey, CT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (03) : 1230 - 1235
  • [5] Telomere instability in a human tumor cell line expressing a dominant-negative WRN protein
    Bai, YL
    Murnane, JP
    [J]. HUMAN GENETICS, 2003, 113 (04) : 337 - 347
  • [6] Telomere states and cell fates
    Blackburn, EH
    [J]. NATURE, 2000, 408 (6808) : 53 - 56
  • [7] Switching and signaling at the telomere
    Blackburn, EH
    [J]. CELL, 2001, 106 (06) : 661 - 673
  • [8] Telomere shortening and tumor formation by mouse cells lacking telomerase RNA
    Blasco, MA
    Lee, HW
    Hande, MP
    Samper, E
    Lansdorp, PM
    DePinho, RA
    Greider, CW
    [J]. CELL, 1997, 91 (01) : 25 - 34
  • [9] BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function
    Cantor, SB
    Bell, DW
    Ganesan, S
    Kass, EM
    Drapkin, R
    Grossman, S
    Wahrer, DCR
    Sgroi, DC
    Lane, WS
    Haber, DA
    Livingston, DM
    [J]. CELL, 2001, 105 (01) : 149 - 160
  • [10] Cheung I, 2002, NAT GENET, V31, P405, DOI [10.1038/417405a, 10.1038/ng928]