Exaptation of Transposable Elements into Novel Cis-Regulatory Elements: Is the Evidence Always Strong?

被引:122
作者
de Souza, Flavio S. J. [1 ,2 ]
Franchini, Lucia F. [1 ]
Rubinstein, Marcelo [1 ,2 ]
机构
[1] Consejo Nacl Invest Cient & Tecn, Inst Invest Ingn Genet & Biol Mol, Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Fisiol Biol Mol & Celular, Buenos Aires, DF, Argentina
关键词
exaptation; enhancer; mobile element; gene expression; HUMAN ENDOGENOUS RETROVIRUS; JUNK DNA; APOLIPOPROTEIN(A) GENE; CONVERGENT EVOLUTION; PURIFYING SELECTION; NEURONAL ENHANCERS; CORE-SINES; IDENTIFICATION; GENOME; EXPRESSION;
D O I
10.1093/molbev/mst045
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
Transposable elements (TEs) are mobile genetic sequences that can jump around the genome from one location to another, behaving as genomic parasites. TEs have been particularly effective in colonizing mammalian genomes, and such heavy TE load is expected to have conditioned genome evolution. Indeed, studies conducted both at the gene and genome levels have uncovered TE insertions that seem to have been co-opted-or exapted-by providing transcription factor binding sites (TFBSs) that serve as promoters and enhancers, leading to the hypothesis that TE exaptation is a major factor in the evolution of gene regulation. Here, we critically review the evidence for exaptation of TE-derived sequences as TFBSs, promoters, enhancers, and silencers/insulators both at the gene and genome levels. We classify the functional impact attributed to TE insertions into four categories of increasing complexity and argue that so far very few studies have conclusively demonstrated exaptation of TEs as transcriptional regulatory regions. We also contend that many genome-wide studies dealing with TE exaptation in recent lineages of mammals are still inconclusive and that the hypothesis of rapid transcriptional regulatory rewiring mediated by TE mobilization must be taken with caution. Finally, we suggest experimental approaches that may help attributing higher-order functions to candidate exapted TEs.
引用
收藏
页码:1239 / 1251
页数:13
相关论文
共 94 条
[11]   Transposable element insertions have strongly affected human evolution [J].
Britten, Roy J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (46) :19945-19948
[12]   The contribution of RNAs and retroposition to evolutionary novelties [J].
Brosius, J .
GENETICA, 2003, 118 (2-3) :99-116
[13]   ON GENOMENCLATURE - A COMPREHENSIVE (AND RESPECTFUL) TAXONOMY FOR PSEUDOGENES AND OTHER JUNK DNA [J].
BROSIUS, J ;
GOULD, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) :10706-10710
[14]   Dioxin receptor and SLUG transcription factors regulate the insulator activity of B1 SINE retrotransposons via an RNA polymerase switch [J].
Carlos Roman, Angel ;
Gonzalez-Rico, Francisco J. ;
Molto, Eduardo ;
Hernando, Henar ;
Neto, Ana ;
Vicente-Garcia, Cristina ;
Ballestar, Esteban ;
Gomez-Skarmeta, Jose L. ;
Vavrova-Anderson, Jana ;
White, Robert J. ;
Montoliu, Lluis ;
Fernandez-Salguero, Pedro M. .
GENOME RESEARCH, 2011, 21 (03) :422-432
[15]   Evo-devo and an expanding evolutionary synthesis: A genetic theory of morphological evolution [J].
Carroll, Sean B. .
CELL, 2008, 134 (01) :25-36
[16]   Rodent Evolution: Back to the Root [J].
Churakov, Gennady ;
Sadasivuni, Manoj K. ;
Rosenbloom, Kate R. ;
Huchon, Dorothee ;
Brosius, Juergen ;
Schmitz, Juergen .
MOLECULAR BIOLOGY AND EVOLUTION, 2010, 27 (06) :1315-1326
[17]   Endogenous retroviral LTRs as promoters for human genes: A critical assessment [J].
Cohen, Carla J. ;
Lock, Wynne M. ;
Mager, Dixie L. .
GENE, 2009, 448 (02) :105-114
[18]   Evolutionary history of the human endogenous retrovirus family ERV9 [J].
Costas, J ;
Naveira, H .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (02) :320-330
[19]   Identification of neuronal enhancers of the proopiomelanocortin gene by transgenic mouse analysis and phylogenetic footprinting [J].
de Souza, FSJ ;
Santangelo, AM ;
Bumaschny, V ;
Avale, ME ;
Smart, JL ;
Low, MJ ;
Rubinstein, M .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (08) :3076-3086
[20]   Is junk DNA bunk? A critique of ENCODE [J].
Doolittle, W. Ford .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (14) :5294-5300