Isodicentric X chromosome in a patient with Turner syndrome — implications for localization of the X-inactivation center
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Summary
Cytogenetic analyses have previously shown that the region Xq11.2–q21 is retained in all structurally abnormal X chromosomes. From these observations the conclusion has been drawn that this “critical region” on the proximal long arm of the X chromosome contains the locus controlling X-inactivation. Structurally abnormal X chromosomes without the X-inactivation center would allow nullisomy, disomy, or trisomy for genes on the X chromosome, and this condition is presumed nonviable. We studied a 28-year-old woman with primary amenorrhea and features of Turner syndrome who had an unusual isodicentric chromosome of the short arm of X. This patient provided us with the opportunity to more closely define the location of the X-inactivation center. High resolution chromosome analysis showed a 46,X,idic(X)(pter→q13.2::q13.2→pter) chromosome pattern in 94% of her cells and a 45,X complement in 6%. Replication studies showed this derivative X chromosome to be late-replicating (inactive) in all cells analyzed. DNA analysis confirmed the breakpoint of the isodicentric chromosome to be proximal to PGK1. Based on these results, the locus for the X-inactivation center can be refined to be within Xq11.2–q13.2.
Keywords
Internal Medicine High Resolution Metabolic Disease Critical Region Cytogenetic AnalysisPreview
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References
- Berghe H van den, Fryns JP, Devos F (1973) 46,XXip karyotype in a woman with normal stature and gonadal dysgenesis without other congenital anomalies. Humangenetik 20:163–166Google Scholar
- Brown CJ, Willard HF (1989) Localization of the X-inactivation center (XIC) to Xq13. Cytogenet Cell Genet 51:971 (A2633)Google Scholar
- Brown CJ, Lafreniere RG, Powers VE, Sebastio G, Ballabio A, Pettigrew AL, Ledbetter DH, Levy E, Craig IW, Willard HF (1991) Localization of the X inactivation centre on the human X chromosome in Xq13. Nature 349:82–84Google Scholar
- Caspersson T, Lindsten J, Zech L (1970) The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis. Hereditas 66:287–291Google Scholar
- Chapelle A de la, Schroder J, Pernu M (1972) Isochromosome for the short arm of X, a human 46,XXpi syndrome. Ann Hum Genet 36:79–87Google Scholar
- Flejter WL, Van Dyke DL, Weiss L (1984) Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center. Am J Hum Genet 36:218–226Google Scholar
- Hook EB, Warburton D (1983) The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence of diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism. Hum Genet 64:24–27Google Scholar
- Kaffe S, Hsu LYF, Hirschhorn K (1983) Structural abnormalities of the human X chromosome and their clinical features. In: Sandberg AA (ed) Cytogenetics of the mammalian X chromosome, part B. Liss, New York, pp 341–358Google Scholar
- Laskey RA, Mills AD (1977) Enhanced autoradiographic detection of 32P and 125I using intensifying screens and hypersensitized film. FEBS Lett 82:314–316Google Scholar
- Mandel J-L, Willard HF, Nussbaum RL, Romero G, Puck JM, Davies KE (1989) Report of the commitee on the genetic constitution of the X chromosome. (10th International Workshop on Human Gene Mapping) Cytogenet Cell Genet 51:384–437Google Scholar
- Maniatis T, Frisch EF, Sambrook J (1982) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NYGoogle Scholar
- Mattei MG, Mattei JF, Vidail F, Giraud F (1981) Structural anomalies of the X chromosome and inactivation center. Hum Genet 56:401–408Google Scholar
- Midro AT, Kulikowski M, Sawicka A, Panasiuk B, Korsak E (1988) Familial occurrence of isodicentric X chromosomes with different breakpoints. Clin Genet 34:153–160Google Scholar
- Perry P, Wolff S (1974) New Giemsa method for the differential staining of sister chromatids. Nature 251:156–158Google Scholar
- Rocchi M, Archidiacono N, Bertorello M, Neri C, Forabosco A (1989) The human X inactivation center is located in the region Xcen→q12. 2. Cytogenet Cell Genet 51:1066Google Scholar
- Therman E, Patau K (1974) Abnormal X chromosomes in man: origin, behavior and effects. Humangenetik 25:1–16Google Scholar
- Therman E, Sarto GE (1983) Inactivation center on the human X chromosome. In: Sandberg AA (ed) Cytogenetics of the mammalian X chromosome, part A. Liss, New York, pp 315–325Google Scholar
- Therman E, Sarto GE, Palmer CG, Kallio H, Denniston C (1979) Position of the human X inactivation center on Xq. Hum Genet 50:59–64Google Scholar
- Van Dyke DL, Flejter WL, Worsham MJ, Roberson JR, Higgins JV, Herr HM, Knuutila S, Wang N, Babu VR, Weiss L (1986) A practical metaphase marker of the inactive X chromosome. Am J Hum Genet 30:88–95Google Scholar