Evidence of extensive non-allelic gene conversion among LTR elements in the human genome

被引:24
作者
Trombetta, Beniamino [1 ]
Fantini, Gloria [1 ]
D'Atanasio, Eugenia [1 ]
Sellitto, Daniele [2 ]
Cruciani, Fulvio [1 ,2 ,3 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Biol Biotecnol Charles Darwin, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[2] CNR, Ist Biol & Patol Mol, Rome, Italy
[3] Univ Roma La Sapienza, Fdn Cenci Bolognetti, Ist Pasteur, Piazzale Aldo Moro 5, I-00185 Rome, Italy
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
HUMAN ENDOGENOUS RETROVIRUSES; STRAND BREAK REPAIR; HUMAN Y-CHROMOSOME; RECURRENT MUTATION; HAPLOGROUP E3B; HERV-W; RECOMBINATION; EVOLUTION; DYNAMICS; INSIGHTS;
D O I
10.1038/srep28710
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 Terminal Repeats (LTRs) are nearly identical DNA sequences found at either end of Human Endogenous Retroviruses (HERVs). The high sequence similarity that exists among different LTRs suggests they could be substrate of ectopic gene conversion events. To understand the extent to which gene conversion occurs and to gain new insights into the evolutionary history of these elements in humans, we performed an intra-species phylogenetic study of 52 LTRs on different unrelated Y chromosomes. From this analysis, we obtained direct evidence that demonstrates the occurrence of ectopic gene conversion in several LTRs, with donor sequences located on both sex chromosomes and autosomes. We also found that some of these elements are characterized by an extremely high density of polymorphisms, showing one of the highest nucleotide diversities in the human genome, as well as a complex patchwork of sequences derived from different LTRs. Finally, we highlighted the limits of current short-read NGS studies in the analysis of genetic diversity of the LTRs in the human genome. In conclusion, our comparative re-sequencing analysis revealed that ectopic gene conversion is a common event in the evolution of LTR elements, suggesting complex genetic links among LTRs from different chromosomes.
引用
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页数:11
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共 57 条
[1]   The case of the unreliable SNP: Recurrent back-mutation of Y-chromosomal marker P25 through gene conversion [J].
Adams, Susan M. ;
King, Turi E. ;
Bosch, Elena ;
Jobling, Mark A. .
FORENSIC SCIENCE INTERNATIONAL, 2006, 159 (01) :14-20
[2]   Pathophysiological Role of HERV-W in Schizophrenia [J].
Aftab, Awais ;
Shah, Asim A. ;
Hashmi, Ali Madeeh .
JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES, 2016, 28 (01) :17-25
[3]   The evolutionary dynamics of human endogenous retroviral families [J].
Bannert, Norbert ;
Kurth, Reinhard .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2006, 7 :149-173
[4]   Rate of recombinational deletion among human endogenous retroviruses [J].
Belshaw, Robert ;
Watson, Jason ;
Katzourakis, Aris ;
Howe, Alexis ;
Woolven-Allen, John ;
Burt, Austin ;
Tristem, Michael .
JOURNAL OF VIROLOGY, 2007, 81 (17) :9437-9442
[5]   Dynamics of a human interparalog gene conversion hotspot [J].
Bosch, E ;
Hurles, ME ;
Navarro, A ;
Jobling, MA .
GENOME RESEARCH, 2004, 14 (05) :835-844
[6]   HLA DNA Sequence Variation among Human Populations: Molecular Signatures of Demographic and Selective Events [J].
Buhler, Stephane ;
Sanchez-Mazas, Alicia .
PLOS ONE, 2011, 6 (02)
[7]   Gene conversion: mechanisms, evolution and human disease [J].
Chen, Jian-Min ;
Cooper, David N. ;
Chuzhanova, Nadia ;
Ferec, Claude ;
Patrinos, George P. .
NATURE REVIEWS GENETICS, 2007, 8 (10) :762-775
[8]   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
[9]   The impact of retrotransposons on human genome evolution [J].
Cordaux, Richard ;
Batzer, Mark A. .
NATURE REVIEWS GENETICS, 2009, 10 (10) :691-703
[10]   Phylogeographic analysis of haplogroup E3b (E-M215) Y chromosomes reveals multiple migratory events within and out of Africa [J].
Cruciani, F ;
La Fratta, R ;
Santolamazza, P ;
Sellitto, D ;
Pascone, R ;
Moral, P ;
Watson, E ;
Guida, V ;
Colomb, EB ;
Zaharova, B ;
Lavinha, J ;
Vona, G ;
Aman, R ;
Calì, F ;
Akar, N ;
Richards, M ;
Torroni, A ;
Novelletto, A ;
Scozzari, R .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (05) :1014-1022