Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia

Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and...

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Veröffentlicht in:American journal of medical genetics 1997-05, Vol.70 (2), p.134-137
Hauptverfasser: Liou, Jui-Der, Ma, Yen-Ying, Gibson, Lisa H., Su, Hua, Charest, Nancy, Lau, Yun-Fai Chris, Yang-Feng, Teresa L.
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container_issue 2
container_start_page 134
container_title American journal of medical genetics
container_volume 70
creator Liou, Jui-Der
Ma, Yen-Ying
Gibson, Lisa H.
Su, Hua
Charest, Nancy
Lau, Yun-Fai Chris
Yang-Feng, Teresa L.
description Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and lie within interval 5B of the Y chromosome. PCR and sequence analysis indicated that our patient carries a normal SRY gene. For an additional comparison of the patient's inv(Y) with the father, two other Y chromosome sequences were examined. Molecular studies of this familial inverted Y chromosome showed no differences in the ZFY and TSPY genes between the father and the patient suggesting that the short arm of our patient's inv(Y) is identical to that of the patient's father. Southern analysis using a probe of the DAX‐1 gene indicated that a single copy of DSS (dosage sensitive sex reversal) locus was present in the patient. Our results suggest that the abnormal sexual development in our patient is likely attributable to (an)other mechanism(s) than mutation in the SRY gene and dosage alteration of the DAX‐1 gene. Am. J. Med. Genet. 70:134–137, 1997. © 1997 Wiley‐Liss, Inc.
doi_str_mv 10.1002/(SICI)1096-8628(19970516)70:2<134::AID-AJMG6>3.0.CO;2-Y
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FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and lie within interval 5B of the Y chromosome. PCR and sequence analysis indicated that our patient carries a normal SRY gene. For an additional comparison of the patient's inv(Y) with the father, two other Y chromosome sequences were examined. Molecular studies of this familial inverted Y chromosome showed no differences in the ZFY and TSPY genes between the father and the patient suggesting that the short arm of our patient's inv(Y) is identical to that of the patient's father. Southern analysis using a probe of the DAX‐1 gene indicated that a single copy of DSS (dosage sensitive sex reversal) locus was present in the patient. Our results suggest that the abnormal sexual development in our patient is likely attributable to (an)other mechanism(s) than mutation in the SRY gene and dosage alteration of the DAX‐1 gene. Am. J. Med. 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J. Med. Genet</addtitle><description>Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and lie within interval 5B of the Y chromosome. PCR and sequence analysis indicated that our patient carries a normal SRY gene. For an additional comparison of the patient's inv(Y) with the father, two other Y chromosome sequences were examined. Molecular studies of this familial inverted Y chromosome showed no differences in the ZFY and TSPY genes between the father and the patient suggesting that the short arm of our patient's inv(Y) is identical to that of the patient's father. Southern analysis using a probe of the DAX‐1 gene indicated that a single copy of DSS (dosage sensitive sex reversal) locus was present in the patient. Our results suggest that the abnormal sexual development in our patient is likely attributable to (an)other mechanism(s) than mutation in the SRY gene and dosage alteration of the DAX‐1 gene. Am. J. Med. 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subjects ambiguous genitalia
Biological and medical sciences
Chromosome aberrations
Chromosome Inversion
Disorders of Sex Development
familial
Gonadal Dysgenesis, 46,XY - genetics
Humans
In Situ Hybridization, Fluorescence
Infant, Newborn
inverted Y
Male
Medical genetics
Medical sciences
Y Chromosome - genetics
title Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia
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