The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned (original) (raw)
Bull, J.J. Evolution of Sex Determining Mechanisms (Benjamin Cummings, Menlo Park, California, 1983). Google Scholar
Charlesworth, B. The evolution of chromosomal sex determination and dosage compensation. Curr Biol.6, 149–162 (1996). ArticleCAS Google Scholar
Ohno, S. Sex Chromosomes and Sex-Linked genes (Springer Verlag, Berlin, 1967). Book Google Scholar
Rice, W.R. Evolution of the Y sex chromosome in animals. BioScience46, 331–343 (1996). Article Google Scholar
Rice, W.R. Degeneration of a nonrecombining chromosome. Science263, 230–232 (1994). ArticleCAS Google Scholar
Steinemann, M. & Steinemann, S. Degenerating Y chromosome of Drosophila miranda: a trap for retroposons. Proc. Natl. Acad. Sci. USA89, 7591–7595 (1992). ArticleCAS Google Scholar
Graves, J.A.M. The origin and function of the mammalian Y chromosome and Y-borne genes — an evolving understanding. BioEssays17, 311–321 (1995). ArticleCAS Google Scholar
Fisher, R.A. The evolution of dominance. Biol. Rev.6, 345–368 (1931). Article Google Scholar
Burgoyne, P.S. Fruit (less) flies provide a clue. Nature381, 740–741 (1996). ArticleCAS Google Scholar
Tiepolo, L. & Zuffardi, 0. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the Y chromosome long arm. Hum. Genet.34, 119–124 (1976). ArticleCAS Google Scholar
Vergnaud, G. et al. A deletion map of the human Y chromosome based on DNA hybridization. Am. J. Hum. Genet.38, 109–124 (1986). CASPubMedPubMed Central Google Scholar
Vollrath, D. et al. The human Y chromosome: a 43-interval map based on naturally occurring deletions. Science258, 52–59 (1992). ArticleCAS Google Scholar
Foote, S., Vollrath, D., Hilton, A. & Page, D.C. The human Y chromosome: overlapping DNA clones spanning the euchromatic region. Science258, 60–66 (1992). ArticleCAS Google Scholar
Johnson, M.D., Tho, S.P.T., Behzadian, A. & McDonough, P.G. Molecular scanning of Yq11 (interval 6) in men with Sertoli-cell-only syndrome. Am. J. Obstet Gynecol.161, 1732–1737 (1989). ArticleCAS Google Scholar
Skare, J. et al. Interstitial deletion involving most of Yq. Am. J. Med. Genet.36, 394–397 (1990). ArticleCAS Google Scholar
Ma, K. et al. Towards the molecular localisation of the AZF locus: mapping of microdeietions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome. Hum. Molec. Genet.1, 29–33 (1992). ArticleCAS Google Scholar
Vogt, P.H. et al. Human Y chromosome Azoospermia Factors (AZF) mapped to different subregions in Yq11. Hum. Molec. Genet.5, 933–943 (1996). ArticleCAS Google Scholar
Reijo, R. et al. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nature Genet.10, 383–393 (1995). ArticleCAS Google Scholar
Reijo, R., Alagappan, R.K., Patrizio, P. & Page, D.C. Severe oligospermia resulting from deletions of Azoospermia Factor gene on Y chromosome. The Lancet347, 1290–1293 (1996). ArticleCAS Google Scholar
Menke, D., Mutter, G. & Page, D.C. Expression of DAZ, an Azoospermia Factor candidate, in human spermatogonia. Am. J. Hum. Genet, (in the press).
Eberhart, C.G., Maines, J.Z. & Wasserman, S.A. Meiotic cell cycle requirement for a fly homologue of human Deleted in Azoospermia. Nature381, 783–785 (1996). ArticleCAS Google Scholar
Reijo, R. et al. Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty. Genomics35, 346–352 (1996). ArticleCAS Google Scholar
Cooke, H.J. et al. A murine homologue of the human DAZ gene is autosomal and expressed only in male and female gonads. Hum. Mol. Genet.5, 513–516 (1996). ArticleCAS Google Scholar
Bishop, C., Guellaen, G., Geldwerth, D., Fellous, M. & Weissenbach, J. Extensive sequence homologies between Y and other chromosomes. J. Mol. Biol.173, 403–417 (1984). ArticleCAS Google Scholar
Ngo, K.Y., Vergnaud, G., Johnsson, C., Lucotte, G. & Weissenbach, J. A DNA probe detecting multiple haplotypes of the human Y chromosome. Am. J. Hum. Genet.38, 407–418 (1986). CASPubMedPubMed Central Google Scholar
Lucotte, G., Guerin, P., Halle, L., Loirat, F. & Hazout, S. Y chromosome DNA polymorphisms in two African populations. Am. J. Hum. Genet.45, 16–20 (1989). CASPubMedPubMed Central Google Scholar
Santachiara Benerecetti, A.S. et al. The common, Near Eastern origin of Ashkenazi and Sephardi Jews supported by Y-chromosome similarity. Ann. Hum. Genet.57, 55–64 (1993). ArticleCAS Google Scholar
Spurdle, A. & Jenkins, T. Y chromosome probe 49a detects complex Pvull haplotypes and many new Taql haplotypes in southern African populations. Am. J. Hum. Genet.50, 107–125 (1992). CASPubMedPubMed Central Google Scholar
Lucotte, G., David, F. & Mariotti, M. Nucleotide sequence of p49a, a genomic Y-specific probe with potential utilization in sex determination. Mol. Cell. Probes5, 359–363 (1991). ArticleCAS Google Scholar
Seboun, E. et al. A molecular approach to the study of the human Y chromosome and anomalies of sex determination in man. Cold Spring Harb. Symp. Quant. Biol.51, 237–248 (1986). ArticleCAS Google Scholar
Affara, N. et al. Report of the second international workshop on Y chromosome mapping 1995. Cytogenet. Cell Genet.73, 33–76 (1996). ArticleCAS Google Scholar
Winge, O. The location of eighteen genes in Lebistes reticulatus. J. Genet.18, 1–43 (1927). Article Google Scholar
Charlesworth, D. & Charlesworth, B. Sex-differences in fitness and selection for centric fusions between sex chromosomes and autosomes. Genet. Res.35, 205–214 (1980). ArticleCAS Google Scholar
Page, D.C. Hypothesis: a Y-chromosomal gene causes gonadoblastoma in dysgenetic gonads. Development101 Suppl., 151–155 (1987). PubMed Google Scholar
Hackstein, J.H. & Hochstenbach, R. The elusive fertility genes of Drosophila: the ultimate haven for selfish genetic elements. Trends Genet.11, 195–200 (1995). ArticleCAS Google Scholar
Rugarli, E. et al. Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J mice. Nature Genet.10, 466–471 (1995). ArticleCAS Google Scholar
Palmer, S., Perry, J. & Ashworth, A. A contravention of Ohno's law in mice. Nature Genet.10, 472–476 (1995). ArticleCAS Google Scholar
Shizuya, H.B. et al. Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector. Proc. Natl. Acad. Sci. USA89, 8794–8797 (1992). ArticleCAS Google Scholar
Chance, P.F. et al. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell72, 143–151 (1993). ArticleCAS Google Scholar
Gyapay, G. et al. A radiation hybrid map of the human genome. Hum. Mol. Genet.5, 339–346 (1996). ArticleCAS Google Scholar
Hudson, T.J. et al. An STS-based map of the human genome. Science270, 1945–1954 (1995). ArticleCAS Google Scholar
Burd, C.G. & Dreyfuss, G. Conserved structures and diversity of functions of RNA binding proteins. Science265, 615–621 (1994). ArticleCAS Google Scholar
Kenan, D.J., Query, C.C. & Keene, J.D. RNA recognition: towards identifying determinants of specificity. Trends Biochem.16, 214–220 (1991). ArticleCAS Google Scholar