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H-Y antigen in X,i(Xq) gonadal dysgenesis: Evidence of X-linked genes in testicular differentiation
Authors:Stephen S. Wachtel  Gloria C. Koo  W. Roy Breg  Myron Genel
Affiliation:(1) Memorial Sloan-Kettering Cancer Center, 10021 New York, NY, USA;(2) Department of Pediatrics, New York Hospital-Cornell Medical Center, 10021 New York, NY, USA;(3) Department of Human Genetics, Yale University School of Medicine, 06510 New Haven, Connecticut, USA;(4) Department of Pediatrics, Yale University School of Medicine, 06510 New Haven, Connecticut, USA;(5) Sloan-Kettering Institute, 1275 York Avenue, 10021 New York, NY, USA
Abstract:Summary Three years ago, we detected H-Y antigen in the white blood cells of a phenotypic female with several of the stigmata of Turner's syndrome, and the mosaic karyotype: 45,X/46,X,i(Xq). We surmised at the time that the isochromosome, i(Xq), may have contained occult Y-chromosome-derived material. We have now confirmed the presence of H-Y in this patient and we have obtained evidence for the presence of H-Y in four of five other similar patients, all of whom are notable for carrying at least a single cell line with the karyotype 46,X,i(Xq). Although we cannot categorically exclude the presence of Y-chromosomal genes in the cells of these patients, there is no cytogenetic evidence of structural rearrangement involving the Y in any of the cases. Expression of H-Y antigen in association with i(Xq) thus implies that H-Y structural genes are X-situated, or alternatively that they are autosomal and X-regulated. It would follow that the H-Y+ cellular phenotype per se is not a valid marker for the Y-chromosome, and that H-Y genes that have been mapped to the pericentric region of the Y may be regulatory.
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