Using Alu Elements as Polyadenylation Sites: A Case of Retroposon Exaptation

被引:73
作者
Chen, Chongjian [1 ,2 ]
Ara, Takeshi [3 ]
Gautheret, Daniel [1 ]
机构
[1] Univ Paris 11, Inst Genet & Microbiol, CNRS, UMR 8621, F-91405 Orsay, France
[2] Zhongshan Univ, Key Lab Gene Engn, State Key Lab Biocontrol, Minist Educ, Guangzhou, Guangdong, Peoples R China
[3] Kazusa DNA Res Inst, Chiba, Japan
关键词
MESSENGER-RNA POLYADENYLATION; HUMAN GENOME; TRANSPOSABLE ELEMENTS; UNTRANSLATED REGIONS; SELECTION; SIGNALS; GENES; RETROTRANSPOSON; EVOLUTION; SEQUENCES;
D O I
10.1093/molbev/msn249
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
Of the 1.1 million Alu retroposons in the human genome, about 10,000 are inserted in the 3' untranslated regions (UTR) of protein-coding genes and 1% of these (107 events) are active as polyadenylation sites (PASs). Strikingly, although Alu's in 3' UTR are indifferently inserted in the forward or reverse direction, 99% of polyadenylation-active Alu sequences are forward oriented. Consensus Alu+ sequences contain sites that can give rise to polyadenylation signals and enhancers through a few point mutations. We found that the strand bias of polyadenylation-active Alu's reflects a radical difference in the fitness of sense and antisense Alu's toward cleavage/polyadenylation activity. In contrast to previous beliefs, Alu inserts do not necessarily represent weak or cryptic PASs; instead, they often constitute the major or the unique PAS in a gene, adding to the growing list of Alu exaptations. Finally, some Alu-borne PASs are intronic and produce truncated transcripts that may impact gene function and/or contribute to gene remodeling.
引用
收藏
页码:327 / 334
页数:8
相关论文
共 33 条
[1]   The association of Alu repeats with the generation of potential AU-rich elements (ARE) at 3′ untranslated regions. -: art. no. 97 [J].
An, HJ ;
Lee, D ;
Lee, KH ;
Bhak, J .
BMC GENOMICS, 2004, 5 (1)
[2]   Alu repeats and human genomic diversity [J].
Batzer, MA ;
Deininger, PL .
NATURE REVIEWS GENETICS, 2002, 3 (05) :370-379
[3]   Patterns of variant polyadenylation signal usage in human genes [J].
Beaudoing, E ;
Freier, S ;
Wyatt, JR ;
Claverie, JM ;
Gautheret, D .
GENOME RESEARCH, 2000, 10 (07) :1001-1010
[4]   A distal enhancer and an ultraconserved exon are derived from a novel retroposon [J].
Bejerano, G ;
Lowe, CB ;
Ahituv, N ;
King, B ;
Siepel, A ;
Salama, SR ;
Rubin, EM ;
Kent, WJ ;
Haussler, D .
NATURE, 2006, 441 (7089) :87-90
[5]   Targeting a complex transcriptome: The construction of the mouse full-length cDNA encyclopedia [J].
Carninci, P ;
Waki, K ;
Shiraki, T ;
Konno, H ;
Shibata, K ;
Itoh, M ;
Aizawa, K ;
Arakawa, T ;
Ishii, Y ;
Sasaki, D ;
Bono, H ;
Kondo, S ;
Sugahara, Y ;
Saito, R ;
Osato, N ;
Fukuda, S ;
Sato, K ;
Watahiki, A ;
Hirozane-Kishikawa, T ;
Nakamura, M ;
Shibata, Y ;
Yasunishi, A ;
Kikuchi, N ;
Yoshiki, A ;
Kusakabe, M ;
Gustincich, S ;
Beisel, K ;
Pavan, W ;
Aidinis, V ;
Nakagawara, A ;
Held, WA ;
Iwata, H ;
Kono, T ;
Nakauchi, H ;
Lyons, P ;
Wells, C ;
Hume, DA ;
Fagiolini, M ;
Hensch, TK ;
Brinkmeier, M ;
Camper, S ;
Hirota, J ;
Mombaerts, P ;
Muramatsu, M ;
Okazaki, Y ;
Kawai, J ;
Hayashizaki, Y .
GENOME RESEARCH, 2003, 13 (6B) :1273-1289
[6]   Mechanism and regulation of mRNA polyadenylation [J].
Colgan, DF ;
Manley, JL .
GENES & DEVELOPMENT, 1997, 11 (21) :2755-2766
[7]   MUSCLE: multiple sequence alignment with high accuracy and high throughput [J].
Edgar, RC .
NUCLEIC ACIDS RESEARCH, 2004, 32 (05) :1792-1797
[8]   EXAPTATION - A MISSING TERM IN THE SCIENCE OF FORM [J].
GOULD, SJ ;
VRBA, ES .
PALEOBIOLOGY, 1982, 8 (01) :4-15
[9]   In silico detection of control signals:: mRNA 3′-end-processing sequences in diverse species [J].
Graber, JH ;
Cantor, CR ;
Mohr, SC ;
Smith, TF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :14055-14060
[10]   Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes [J].
Han, JS ;
Szak, ST ;
Boeke, JD .
NATURE, 2004, 429 (6989) :268-274