Report of a chimeric origin of transposable elements in a bovine-coding gene

被引:2
作者
Almeida, L. M. [1 ]
Amaral, M. E. J. [1 ]
Silva, I. T. [2 ]
Silva, W. A., Jr. [2 ]
Riggs, P. K. [3 ]
Carareto, C. M. [1 ]
机构
[1] Univ Estado Sao Paulo, IBILCE, Dept Biol, Sao Jose De Rio Preto, SP, Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Genet, Ribeirao Preto, SP, Brazil
[3] Texas A&M Univ, Dept Anim Sci, College Stn, TX 77843 USA
关键词
cow; genome; exaptation; domestication; transposon; FASTKD3;
D O I
10.4238/vol7-1gmr371
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
Despite the wide distribution of transposable elements (TEs) in mammalian genomes, part of their evolutionary significance remains to be discovered. Today there is a substantial amount of evidence showing that TEs are involved in the generation of new exons in different species. In the present study, we searched 22,805 genes and reported the occurrence of TE-cassettes in coding sequences of 542 cow genes using the RepeatMasker program. Despite the significant number (542) of genes with TE insertions in exons only 14 (2.6%) of them were translated into protein, which we characterized as chimeric genes. From these chimeric genes, only the FAST kinase domains 3 (FASTKD3) gene, present on chromosome BTA 20, is a functional gene and showed evidence of the exaptation event. The genome sequence analysis showed that the last exon coding sequence of bovine FASTKD3 is similar to 85% similar to the ART2A retrotransposon sequence. In addition, comparison among FASTKD3 proteins shows that the last exon is very divergent from those of Homo sapiens, Pan troglodytes and Canis familiares. We suggest that the gene structure of bovine FASTKD3 gene could have originated by several ectopic recombinations between TE copies. Additionally, the absence of TE sequences in all other species analyzed suggests that the TE insertion is clade-specific, mainly in the ruminant lineage.
引用
收藏
页码:107 / 116
页数:10
相关论文
共 29 条
[1]   Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system [J].
Agrawal, A ;
Eastman, QM ;
Schatz, DG .
NATURE, 1998, 394 (6695) :744-751
[2]   The contribution of transposable elements to Bos taurus gene structure [J].
Almeida, Luciane M. ;
Silva, Israel T. ;
Silva, Wilson A., Jr. ;
Castro, Juliana P. ;
Riggs, Penny K. ;
Carareto, Claudia M. ;
Amaral, M. Elisabete J. .
GENE, 2007, 390 (1-2) :180-189
[3]   Positional cloning of the mouse retrovirus restriction gene Fv1 [J].
Best, S ;
LeTissier, P ;
Towers, G ;
Stoye, JP .
NATURE, 1996, 382 (6594) :826-829
[4]   Transposable elements as a source of genetic innovation: expression and evolution of a family of retrotransposon-derived neogenes in mammals [J].
Brandt, J ;
Schrauth, S ;
Veith, AM ;
Froschauer, A ;
Haneke, T ;
Schultheis, C ;
Gessler, M ;
Leimeister, C ;
Volff, JN .
GENE, 2005, 345 (01) :101-111
[5]   Coding sequences of functioning human genes derived entirely from mobile element sequences [J].
Britten, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (48) :16825-16830
[6]   Birth of a chimeric primate gene by capture of the transposase gene from a mobile element [J].
Cordaux, Richard ;
Udit, Swalpa ;
Batzer, Mark A. ;
Feschotte, Cedric .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (21) :8101-8106
[7]   Telomerase and retrotransposons: Which came first? [J].
Eickbush, TH .
SCIENCE, 1997, 277 (5328) :911-912
[8]   Evidence for the contribution of LTR retrotransposons to C-elegans gene evolution [J].
Ganko, EW ;
Bhattachajee, V ;
Schliekelman, P ;
McDonald, JF .
MOLECULAR BIOLOGY AND EVOLUTION, 2003, 20 (11) :1925-1931
[9]   Do transposable elements really contribute to proteomes? [J].
Gotea, Valer ;
Makalowski, Wojciech .
TRENDS IN GENETICS, 2006, 22 (05) :260-267
[10]   DNA transposition by the RAG1 and RAG2 proteins: A possible source of oncogenic translocations [J].
Hiom, K ;
Melek, M ;
Gellert, M .
CELL, 1998, 94 (04) :463-470