Distinct mechanisms for trans-mediated mobilization of cellular RNAs by the LINE-1 reverse transcriptase

被引:85
作者
Garcia-Perez, Jose L.
Doucet, Aurelien J.
Bucheton, Alain
Moran, John V.
Gilbert, Nicolas [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
[2] CNRS, UPR 1142, Inst Genet Humaine, F-34396 Montpellier 5, France
[3] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
关键词
D O I
10.1101/gr.5870107
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
Long Interspersed Element-1 (LINE-1 or L1) sequences comprise similar to 17% of human DNA and ongoing L1 retrotransposition continues to impact genome evolution. The L1-encoded proteins also can mobilize other cellular RNAs (e.g., Alu retrotransposons, SVA retrotransposons, and U6 snRNAs), which comprise similar to 13% of human DNA. Here, we demonstrate that the trans-mediated mobilization of non-L1 RNAs can occur by either template choice or template-switching mechanisms. Remarkably, these mechanisms are not mutually exclusive, as both processes can operate sequentially on the same RNA template. Finally, we provide evidence that efficient U6 snRNA retrotransposition requires both ORF1p and ORF2p, providing indirect evidence for the action of ORF1p in U6 snRNA retrotransposition. Thus, we propose that the LINE-1-encoded reverse transcriptase can mediate the retrotransposition of non-L1 RNAs by distinct mechanisms.
引用
收藏
页码:602 / 611
页数:10
相关论文
共 58 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]  
Bennett-Baker PE, 2003, GENETICS, V165, P2055
[3]   Natural genetic variation caused by transposable elements in humans [J].
Bennettt, EA ;
Coleman, LE ;
Tsui, C ;
Pittard, WS ;
Devine, SE .
GENETICS, 2004, 168 (02) :933-951
[4]   Cellular inhibitors of long interspersed element 1 and Alu retrotransposition [J].
Bogerd, Hal P. ;
Wiegand, Heather L. ;
Hulme, Amy E. ;
Garcia-Perez, Jose L. ;
O'Shea, K. Sue ;
Moran, John V. ;
Cullen, Bryan R. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (23) :8780-8785
[5]   RETROPOSONS - SEEDS OF EVOLUTION [J].
BROSIUS, J .
SCIENCE, 1991, 251 (4995) :753-753
[6]   Genomes were forged by massive bombardments with retroelements and retrosequences [J].
Brosius, J .
GENETICA, 1999, 107 (1-3) :209-238
[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]   The human genome contains many types of chimeric retrogenes generated through in vivo RNA recombination [J].
Buzdin, A ;
Gogvadze, E ;
Kovalskaya, E ;
Volchkov, P ;
Ustyugova, S ;
Illarionova, A ;
Fushan, A ;
Vinogradova, T ;
Sverdlov, E .
NUCLEIC ACIDS RESEARCH, 2003, 31 (15) :4385-4390
[9]   A new family of chimeric retrotranscripts formed by a full copy of U6 small nuclear RNA fused to the 3′ terminus of L1 [J].
Buzdin, A ;
Ustyugova, S ;
Gogvadze, E ;
Vinogradova, T ;
Lebedev, Y ;
Sverdlov, E .
GENOMICS, 2002, 80 (04) :402-406
[10]   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