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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1992 Jan;50(1):156–163.

Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.

E Maestrini 1, S Rivella 1, C Tribioli 1, M Rocchi 1, G Camerino 1, S Santachiara-Benerecetti 1, O Parolini 1, L D Notarangelo 1, D Toniolo 1
PMCID: PMC1682517  PMID: 1346076

Abstract

Probes for CpG islands were cloned from the distal long arm of the human X chromosome; three of them were found to be polymorphic. A HindIII RFLP was identified by the probe 2-25 (DXS606), and it was mapped to the Xq27-Xq28 boundary. Probes 2-19 (DXS605) and 2-55 (DXS707), which identify EcoRI and MspI polymorphisms, respectively, have been mapped to the distal part of Xq28, in the G6PD-RCP/GCP gene region. Probe 2-19 has been further localized about 16 kb from the 3' end of the G6PD gene. The new RFLPs may be useful for the precise mapping of the many disease genes localized in this part of the human X chromosome. Probe 2-19 is highly informative, and it has been studied in greater detail. Using the methylation-sensitive rare-cutter enzyme EagI in conjunction with the polymorphic EcoRI site, we were able to demonstrate that the RFLP may be used both to study randomness of X chromosome inactivation and for carrier detection in X-linked syndromes where nonrandom X inactivation occurs. It is conceivable that the combined use of 2-19 and of the probes described so far (pSPT-PGK and M27 beta) will make analysis of X inactivation feasible in virtually every female.

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Selected References

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  1. Alcalay M., Toniolo D. CpG islands of the X chromosome are gene associated. Nucleic Acids Res. 1988 Oct 25;16(20):9527–9543. doi: 10.1093/nar/16.20.9527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beutler E. Glucose-6-phosphate dehydrogenase deficiency. N Engl J Med. 1991 Jan 17;324(3):169–174. doi: 10.1056/NEJM199101173240306. [DOI] [PubMed] [Google Scholar]
  3. Brown R. M., Fraser N. J., Brown G. K. Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked gene. Genomics. 1990 Jun;7(2):215–221. doi: 10.1016/0888-7543(90)90543-4. [DOI] [PubMed] [Google Scholar]
  4. Conley M. E., Lavoie A., Briggs C., Brown P., Guerra C., Puck J. M. Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency. Proc Natl Acad Sci U S A. 1988 May;85(9):3090–3094. doi: 10.1073/pnas.85.9.3090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Conley M. E., Puck J. M. Definition of the gene loci in X-linked immunodeficiencies. Immunol Invest. 1988 Jul;17(5):425–463. doi: 10.3109/08820138809049847. [DOI] [PubMed] [Google Scholar]
  6. D'Urso M., Luzzatto L., Perroni L., Ciccodicola A., Gentile G., Peluso I., Persico M. G., Pizzella T., Toniolo D., Vulliamy T. J. An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence. Am J Hum Genet. 1988 May;42(5):735–741. [PMC free article] [PubMed] [Google Scholar]
  7. D'Urso M., Mareni C., Toniolo D., Piscopo M., Schlessinger D., Luzzatto L. Regulation of glucose 6-phosphate dehydrogenase expression in CHO-human fibroblast somatic cell hybrids. Somatic Cell Genet. 1983 Jul;9(4):429–443. doi: 10.1007/BF01543044. [DOI] [PubMed] [Google Scholar]
  8. Fearon E. R., Kohn D. B., Winkelstein J. A., Vogelstein B., Blaese R. M. Carrier detection in the Wiskott Aldrich syndrome. Blood. 1988 Nov;72(5):1735–1739. [PubMed] [Google Scholar]
  9. Fearon E. R., Winkelstein J. A., Civin C. I., Pardoll D. M., Vogelstein B. Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation. N Engl J Med. 1987 Feb 19;316(8):427–431. doi: 10.1056/NEJM198702193160802. [DOI] [PubMed] [Google Scholar]
  10. Fraser N. J., Boyd Y., Craig I. Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22. Genomics. 1989 Jul;5(1):144–148. doi: 10.1016/0888-7543(89)90099-2. [DOI] [PubMed] [Google Scholar]
  11. Gealy W. J., Dwyer J. M., Harley J. B. Allelic exclusion of glucose-6-phosphate dehydrogenase in platelets and T lymphocytes from a Wiskott-Aldrich syndrome carrier. Lancet. 1980 Jan 12;1(8159):63–65. doi: 10.1016/s0140-6736(80)90492-4. [DOI] [PubMed] [Google Scholar]
  12. Goodship J., Malcolm S., Lau Y. L., Pembrey M. E., Levinsky R. J. Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiency. Lancet. 1988 Apr 2;1(8588):729–732. doi: 10.1016/s0140-6736(88)91537-1. [DOI] [PubMed] [Google Scholar]
  13. Greer W. L., Kwong P. C., Peacocke M., Ip P., Rubin L. A., Siminovitch K. A. X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defect. Genomics. 1989 Jan;4(1):60–67. doi: 10.1016/0888-7543(89)90315-7. [DOI] [PubMed] [Google Scholar]
  14. Guioli S., Arveiler B., Bardoni B., Notarangelo L. D., Panina P., Duse M., Ugazio A., Oberlé I., de Saint Basile G., Mandel J. L. Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia. Hum Genet. 1989 Dec;84(1):19–21. doi: 10.1007/BF00210664. [DOI] [PubMed] [Google Scholar]
  15. Keith D. H., Singer-Sam J., Riggs A. D. Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase. Mol Cell Biol. 1986 Nov;6(11):4122–4125. doi: 10.1128/mcb.6.11.4122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lyon M. F. X-chromosome inactivation and developmental patterns in mammals. Biol Rev Camb Philos Soc. 1972 Jan;47(1):1–35. doi: 10.1111/j.1469-185x.1972.tb00969.x. [DOI] [PubMed] [Google Scholar]
  17. Maestrini E., Rivella S., Tribioli C., Purtilo D., Rocchi M., Archidiacono N., Toniolo D. Probes for CpG islands on the distal long arm of the human X chromosome are clustered in Xq24 and Xq28. Genomics. 1990 Dec;8(4):664–670. doi: 10.1016/0888-7543(90)90253-q. [DOI] [PubMed] [Google Scholar]
  18. Manoni M., Tribioli C., Lazzari B., DeBellis G., Patrosso C., Pergolizzi R., Pellegrini M., Maestrini E., Rivella S., Vezzoni P. The nucleotide sequence of a CpG island demonstrates the presence of the first exon of the gene encoding the human lysosomal membrane protein lamp2 and assigns the gene to Xq24. Genomics. 1991 Mar;9(3):551–554. doi: 10.1016/0888-7543(91)90424-d. [DOI] [PubMed] [Google Scholar]
  19. Martini G., Toniolo D., Vulliamy T., Luzzatto L., Dono R., Viglietto G., Paonessa G., D'Urso M., Persico M. G. Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase. EMBO J. 1986 Aug;5(8):1849–1855. doi: 10.1002/j.1460-2075.1986.tb04436.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Rosenstraus M., Chasin L. A. Isolation of mammalian cell mutants deficient in glucose-6-phosphate dehydrogenase activity: linkage to hypoxanthine phosphoribosyl transferase. Proc Natl Acad Sci U S A. 1975 Feb;72(2):493–497. doi: 10.1073/pnas.72.2.493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Suthers G. K., Hyland V. J., Callen D. F., Oberle I., Rocchi M., Thomas N. S., Morris C. P., Schwartz C. E., Schmidt M., Ropers H. H. Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. Am J Hum Genet. 1990 Aug;47(2):187–195. [PMC free article] [PubMed] [Google Scholar]
  22. Toniolo D., D'Urso M., Martini G., Persico M., Tufano V., Battistuzzi G., Luzzatto L. Specific methylation pattern at the 3' end of the human housekeeping gene for glucose 6-phosphate dehydrogenase. EMBO J. 1984 Sep;3(9):1987–1995. doi: 10.1002/j.1460-2075.1984.tb02080.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Wolf S. F., Jolly D. J., Lunnen K. D., Friedmann T., Migeon B. R. Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation. Proc Natl Acad Sci U S A. 1984 May;81(9):2806–2810. doi: 10.1073/pnas.81.9.2806. [DOI] [PMC free article] [PubMed] [Google Scholar]

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