Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination.

The human X and Y chromosomes share many blocks of similar DNA sequence. We conducted mapping and nucleotide sequencing studies of extensive, multi-megabase homologies between Yp and Xq21, which do not recombine during male meiosis. We confirmed and built upon previous evidence that a Yp inversion had occurred during evolution: a single contiguous segment of Xq21 is homologous to two non-contiguous segments of Yp. We precisely defined and sequenced the inversion breakpoints, obtaining evidence that the inversion was mediated by recombination between LINE-1 elements in otherwise non-homologous regions. This inversion appears to have followed a single transposition of an approximately 4 Mb segment from the X to the Y chromosome. These events jointly account for the present arrangement of Yp-Xq21 homologous sequences. Based on Southern blotting studies of primates and of humans drawn from diverse populations, we conclude that both the X-Y transposition and the subsequent, LINE-mediated Yp inversion occurred after the divergence of hominid and chimp lineages but before the radiation of extant human populations. This evolutionary scenario is consistent with our finding of 99.3 +/- 0.2% nucleotide identity between the X and Y chromosomes within the transposed region, which suggests that the transposition occurred approximately 3-4 million years ago, near the time of emergence of Homo . Comparative sequencing of the entire human X and Y chromosomes may reveal a succession of transpositions, inversions and other rearrangements underlying the complex pattern of sequence similarities between the present-day sex chromosomes. With the possible exception of cubitus valgus, phenotypic features of Turner syndrome are absent in individuals monosomic for Yp-Xq21 homologous sequences, suggesting that most of the critical 'Turner genes' are found elsewhere on the X and Y chromosomes.

[1]  D. Page,et al.  Functional coherence of the human Y chromosome. , 1997, Science.

[2]  D. Schlessinger,et al.  Evolutionary features of the 4-Mb Xq21.3 XY homology region revealed by a map at 60-kb resolution. , 1997, Genome research.

[3]  Peter Beighton,et al.  de la Chapelle, A. , 1997 .

[4]  C. Wills Another nail in the coffin of the multiple-origins theory? , 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

[5]  S. Rozen,et al.  The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned , 1996, Nature Genetics.

[6]  S. Pääbo,et al.  The genetical archaeology of the human genome , 1996, Nature Genetics.

[7]  N. Affara,et al.  The sequence organization of Yp/proximal Xq homologous regions of the human sex chromosomes is highly conserved. , 1996, Genomics.

[8]  Yun-Fai Chris Lau,et al.  Report of the Second International Workshop on Y Chromosome Mapping 1995. , 1994 .

[9]  T. Bech-Hansen Report of the Sixth International Workshop on Human X Chromosome Mapping 1995 , 1995 .

[10]  A. Monaco,et al.  A high-resolution interval map of the q21 region of the human X chromosome. , 1995, Genomics.

[11]  G. Rappold,et al.  The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability. , 1995, Human molecular genetics.

[12]  J. Weissenbach,et al.  High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1). , 1995, Genomics.

[13]  A. Monaco,et al.  Report of the sixth international workshop on X chromosome mapping 1995 , 1995 .

[14]  M. Ferguson-Smith,et al.  A set of ninety-seven overlapping yeast artificial chromosome clones spanning the human Y chromosome euchromatin. , 1994, Genomics.

[15]  A. Poustka,et al.  Highly homologous loci on the X and Y chromosomes are hot–spots for ectopic recombinations leading to XX maleness , 1994, Nature Genetics.

[16]  W. Brown,et al.  The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes. , 1994, Human molecular genetics.

[17]  Howard J. Cooke,et al.  A Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesis , 1993, Cell.

[18]  J. Schmidtke,et al.  TSPY-related sequences represent a microheterogeneous gene family organized as constitutive elements in DYZ5 tandem repeat units on the human Y chromosome. , 1993, Genomics.

[19]  M. Nei,et al.  Evolutionary relationships of human populations on a global scale. , 1993, Molecular biology and evolution.

[20]  Wen-Hsiung Li,et al.  Male-driven evolution of DNA sequences , 1993, Nature.

[21]  D. Page,et al.  Turner syndrome: the case of the missing sex chromosome. , 1993, Trends in genetics : TIG.

[22]  T Mori,et al.  [Turner syndrome]. , 1993, Ryoikibetsu shokogun shirizu.

[23]  C. Helms,et al.  Identification of a second pseudoautosomal region near the Xq and Yq telomeres. , 1992, Science.

[24]  M. Mitchell,et al.  Evolution of DNA sequence homologies between the sex chromosomes in primate species. , 1992, Genomics.

[25]  D. Page,et al.  The human Y chromosome: overlapping DNA clones spanning the euchromatic region. , 1992, Science.

[26]  P. Beer-Romero,et al.  The human Y chromosome: a 43-interval map based on naturally occurring deletions. , 1992, Science.

[27]  K. Hawkes,et al.  African populations and the evolution of human mitochondrial DNA. , 1991, Science.

[28]  B. Lippe Turner syndrome. , 1991, Endocrinology and metabolism clinics of North America.

[29]  D. Stoppa-Lyonnet,et al.  Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[30]  B. Trask,et al.  Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21. , 1989, American journal of human genetics.

[31]  P. Yen,et al.  The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolution , 1988, Cell.

[32]  F. Cremers,et al.  Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq. , 1988, American journal of human genetics.

[33]  W. Brown A physical map of the human pseudoautosomal region. , 1988, The EMBO journal.

[34]  J. Weissenbach,et al.  Physical mapping of the human pseudo‐autosomal region; comparison with genetic linkage map. , 1988, The EMBO journal.

[35]  H. Lehrach,et al.  A long range restriction map of the pseudoautosomal region by partial digest PFGE analysis from the telomere. , 1988, Nucleic acids research.

[36]  L. Brown,et al.  The sex-determining region of the human Y chromosome encodes a finger protein , 1987, Cell.

[37]  J. Weissenbach,et al.  A sex chromosome rearrangement in a human XX male caused by Alu—Alu recombination , 1987, Cell.

[38]  W. Bickmore,et al.  Evolution of homologous sequences on the human X and Y chromosomes, outside of the meiotic pairing segment. , 1987, Nucleic acids research.

[39]  D. Botstein,et al.  A deletion map of the human Y chromosome based on DNA hybridization. , 1986, American journal of human genetics.

[40]  J. Weissenbach,et al.  A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes , 1986, Nature.

[41]  R. White,et al.  A highly polymorphic locus in human DNA revealed by cosmid-derived probes. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[42]  R. Heilig,et al.  Homologies between X and Y chromosomes detected by DNA probes: localisation and evolution. , 1985, Nucleic acids research.

[43]  J. Weissenbach,et al.  Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome. , 1985, The EMBO journal.

[44]  D. Botstein,et al.  Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution , 1984, Nature.

[45]  J. Weissenbach,et al.  Extensive sequence homologies between Y and other human chromosomes. , 1984, Journal of molecular biology.

[46]  D. Barker,et al.  Restriction sites containing CpG show a higher frequency of polymorphism in human DNA , 1984, Cell.

[47]  A. Feinberg,et al.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum. , 1984, Analytical biochemistry.

[48]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[49]  J. Weissenbach,et al.  Single-copy DNA sequences specific for the human Y chromosome , 1983, Nature.

[50]  D. Botstein,et al.  Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[51]  J. Yunis,et al.  The origin of man: a chromosomal pictorial legacy. , 1982, Science.

[52]  M. Nei,et al.  Mathematical model for studying genetic variation in terms of restriction endonucleases. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[53]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[54]  M. Ferguson-Smith Karyotype-phenotype Correlations in Gonadal Dysgenesis and Their Bearing on the Pathogenesis of Malformations , 1965, Journal of medical genetics.

[55]  H GRUNEBERG,et al.  Human genetics. , 1947, The Eugenics review.