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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1986 May;38(5):751–758.

Quantitative analysis of sex-chromosome mosaicism with X-Y DNA probes.

C M Disteche, H Saal, C Friedman, V Sybert, H Thuline
PMCID: PMC1684831  PMID: 3755007

Abstract

Sex-chromosome mosaicism was quantitatively analyzed in two patients using DNA probes specific for human X and Y chromosomes. Both patients were female with stigmata of the Turner syndrome, and both had a 45,X cell line and a 46,XY cell line. One of the patients had a morphologically abnormal, nonfluorescent Y chromosome, dic(Y)(q11). Hybridization of DNA from this patient with two repetitive DNA sequences specific for the heterochromatic region of the Y chromosome indicated that most of the Y-heterochromatic sequences were deleted. DNA from both patients was hybridized with a probe for the DXYS1 locus and found to have the X- and Y-linked loci. Densitometric measurements of the relative intensities of the X- and Y-linked bands were used to calculate the degree of mosaicism in each case. The percentages of 45,X cells obtained by DNA analysis agreed with those obtained by chromosome analysis. DNA analysis provides a way to quantitate mosaicism at the DNA level and in nondividing tissue.

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Selected References

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  1. Bishop C., Guellaen G., Geldwerth D., Fellous M., Weissenbach J. Extensive sequence homologies between Y and other human chromosomes. J Mol Biol. 1984 Mar 15;173(4):403–417. doi: 10.1016/0022-2836(84)90388-7. [DOI] [PubMed] [Google Scholar]
  2. Bostock C. J., Gosden J. R., Mitchell A. R. Localisation of a male-specific DNA fragment to a sub-region of the human Y chromosome. Nature. 1978 Mar 23;272(5651):324–328. doi: 10.1038/272324a0. [DOI] [PubMed] [Google Scholar]
  3. Bühler E. M. A synopsis of the human Y chromosome. Hum Genet. 1980;55(2):145–175. doi: 10.1007/BF00291764. [DOI] [PubMed] [Google Scholar]
  4. Caspersson T., Hultén M., Jonasson J., Lindsten J., Therkelsen A., Zech L. Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics. Hereditas. 1971;68(2):317–324. doi: 10.1111/j.1601-5223.1971.tb02407.x. [DOI] [PubMed] [Google Scholar]
  5. Cooke H. J., Brown W. A., Rappold G. A. Closely related sequences on human X and Y chromosomes outside the pairing region. Nature. 1984 Sep 20;311(5983):259–261. doi: 10.1038/311259a0. [DOI] [PubMed] [Google Scholar]
  6. Cooke H. Repeated sequence specific to human males. Nature. 1976 Jul 15;262(5565):182–186. doi: 10.1038/262182a0. [DOI] [PubMed] [Google Scholar]
  7. Daiger S. P., Wildin R. S., Su T. S. Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase. Nature. 1982 Aug 12;298(5875):682–684. doi: 10.1038/298682a0. [DOI] [PubMed] [Google Scholar]
  8. Disteche C., Luthy D., Haslam D. B., Hoar D. Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe. Hum Genet. 1984;67(2):222–224. doi: 10.1007/BF00273007. [DOI] [PubMed] [Google Scholar]
  9. GARTLER S. M., LINDER D. SELECTION IN MAMMALIAN MOSAIC CELL POPULATIONS. Cold Spring Harb Symp Quant Biol. 1964;29:253–260. doi: 10.1101/sqb.1964.029.01.028. [DOI] [PubMed] [Google Scholar]
  10. Gänshirt D., Pawlowitzki I. H. Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf). Hum Genet. 1984;67(3):241–244. doi: 10.1007/BF00291348. [DOI] [PubMed] [Google Scholar]
  11. Ikeuchi T. Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome banding. Cytogenet Cell Genet. 1984;38(1):56–61. doi: 10.1159/000132030. [DOI] [PubMed] [Google Scholar]
  12. Kinross J., Fraccaro M., Scappaticci S., Tiepolo L., Zuffardi O., Pawlowitzki I. H., Jones K. W. BSu restriction of DNA from cases exhibiting sex-chromosome abnormalities. Cytogenet Cell Genet. 1978;20(1-6):59–69. doi: 10.1159/000130840. [DOI] [PubMed] [Google Scholar]
  13. Kunkel L. M., Smith K. D., Boyer S. H., Borgaonkar D. S., Wachtel S. S., Miller O. J., Breg W. R., Jones H. W., Jr, Rary J. M. Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Proc Natl Acad Sci U S A. 1977 Mar;74(3):1245–1249. doi: 10.1073/pnas.74.3.1245. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kunkel L. M., Smith K. D., Boyer S. H. Human Y-chromosome-specific reiterated DNA. Science. 1976 Mar 19;191(4232):1189–1190. doi: 10.1126/science.1257744. [DOI] [PubMed] [Google Scholar]
  15. Kunkel L. M., Smith K. D., Boyer S. H. Organization and heterogeneity of sequences within a repeating unit of human Y chromosome deoxyribonucleic acid. Biochemistry. 1979 Jul 24;18(15):3343–3353. doi: 10.1021/bi00582a022. [DOI] [PubMed] [Google Scholar]
  16. Kunkel L. M., Tantravahi U., Eisenhard M., Latt S. A. Regional localization on the human X of DNA segments cloned from flow sorted chromosomes. Nucleic Acids Res. 1982 Mar 11;10(5):1557–1578. doi: 10.1093/nar/10.5.1557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lau Y. F., Huang J. C., Dozy A. M., Kan Y. W. A rapid screening test for antenatal sex determination. Lancet. 1984 Jan 7;1(8367):14–16. doi: 10.1016/s0140-6736(84)90182-x. [DOI] [PubMed] [Google Scholar]
  18. Lau Y. F., Schonberg S. A male-specific DNA probe detects heterochromatin sequences in a familial Yq- chromosome. Am J Hum Genet. 1984 Nov;36(6):1394–1396. [PMC free article] [PubMed] [Google Scholar]
  19. Magenis E., Donlon T. Nonfluorescent Y chromosomes. Cytologic evidence of origin. Hum Genet. 1982;60(2):133–138. doi: 10.1007/BF00569699. [DOI] [PubMed] [Google Scholar]
  20. Page D. C., Harper M. E., Love J., Botstein D. Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution. Nature. 1984 Sep 13;311(5982):119–123. doi: 10.1038/311119a0. [DOI] [PubMed] [Google Scholar]
  21. Page D., de Martinville B., Barker D., Wyman A., White R., Francke U., Botstein D. Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. Proc Natl Acad Sci U S A. 1982 Sep;79(17):5352–5356. doi: 10.1073/pnas.79.17.5352. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Sahar E., Latt S. A. Enhancement of banding patterns in human metaphase chromosomes by energy transfer. Proc Natl Acad Sci U S A. 1978 Nov;75(11):5650–5654. doi: 10.1073/pnas.75.11.5650. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Schweizer D., Ambros P., Andrle M. Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A. Exp Cell Res. 1978 Feb;111(2):327–332. doi: 10.1016/0014-4827(78)90177-5. [DOI] [PubMed] [Google Scholar]
  24. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  25. Wolfe J., Erickson R. P., Rigby P. W., Goodfellow P. N. Regional localization of 3 Y-derived sequences on the human X and Y chromosomes. Ann Hum Genet. 1984 Jul;48(Pt 3):253–259. doi: 10.1111/j.1469-1809.1984.tb01022.x. [DOI] [PubMed] [Google Scholar]

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