Cellular inhibitors of long interspersed element 1 and Alu retrotransposition

被引:300
作者
Bogerd, Hal P.
Wiegand, Heather L.
Hulme, Amy E.
Garcia-Perez, Jose L.
O'Shea, K. Sue
Moran, John V.
Cullen, Bryan R. [1 ]
机构
[1] Duke Univ, Med Ctr, Ctr Virol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[3] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
关键词
APOBEC3; protein; mutagenesis; retrotransposon; genome stability; intrinsic immunity;
D O I
10.1073/pnas.0603313103
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
Long interspersed element (LINE) 1 retrotransposons are major genomic parasites that represent approximate to 17% of the human genome. The LINE-1 ORF2 protein is also responsible for the mobility of Alu elements, which constitute a further approximate to 11% of genomic DNA. Representative members of each element class remain mobile, and deleterious retrotransposition events can induce spontaneous genetic diseases. Here, we demonstrate that APOBEC3A and APOBEC3B, two members of the APOBEC3 family of human innate antiretroviral resistance factors, can enter the nucleus, where LINE-1 and Alu reverse transcription occurs, and specifically inhibit both LINE-1 and Alu retrotransposition. These data suggest that the APOBEC3 protein family may have evolved, at least in part, to defend the integrity of the human genome against endogenous retrotransposons.
引用
收藏
页码:8780 / 8785
页数:6
相关论文
共 45 条
[1]   Unconventional translation of mammalian LINE-1 retrotransposons [J].
Alisch, RS ;
Garcia-Perez, JL ;
Muotri, AR ;
Gage, FH ;
Moran, JV .
GENES & DEVELOPMENT, 2006, 20 (02) :210-224
[2]  
[Anonymous], 2002, MOBILE DNA-UK
[3]   Alu repeats and human genomic diversity [J].
Batzer, MA ;
Deininger, PL .
NATURE REVIEWS GENETICS, 2002, 3 (05) :370-379
[4]   Cytidine deamination of retroviral DNA by diverse APOBEC proteins [J].
Bishop, KN ;
Holmes, RK ;
Sheehy, AM ;
Davidson, NO ;
Cho, SJ ;
Malim, MH .
CURRENT BIOLOGY, 2004, 14 (15) :1392-1396
[5]  
Black BE, 1999, MOL CELL BIOL, V19, P8616
[6]   APOBEC3A and APOBEC3B are potent inhibitors of LTR-retrotransposon function in human cells [J].
Bogerd, HP ;
Wiegand, HL ;
Doehle, BP ;
Lueders, KK ;
Cullen, BR .
NUCLEIC ACIDS RESEARCH, 2006, 34 (01) :89-95
[7]   Hot L1s account for the bulk of retrotransposition in the human population [J].
Brouha, B ;
Schustak, J ;
Badge, RM ;
Lutz-Prigget, S ;
Farley, AH ;
Moran, JV ;
Kazazian, HH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) :5280-5285
[8]   APOBEC3A is a potent inhibitor of adeno-associated virus and retrotransposons [J].
Chen, H ;
Lilley, CE ;
Yu, Q ;
Lee, DV ;
Chou, J ;
Narvaiza, I ;
Landau, NR ;
Weitzman, MD .
CURRENT BIOLOGY, 2006, 16 (05) :480-485
[9]   Human L1 element target-primed reverse transcription in vitro [J].
Cost, GJ ;
Feng, QH ;
Jacquier, A ;
Boeke, JD .
EMBO JOURNAL, 2002, 21 (21) :5899-5910
[10]   Role and mechanism of action of the APOBEC3 family of antiretroviral resistance factors [J].
Cullen, BR .
JOURNAL OF VIROLOGY, 2006, 80 (03) :1067-1076