Literature DB >> 15641705

Analysis of SRY gene in 8 cases of sex abnormality.

Hui Wang1, Yun Teng, Hong Tian, Yanping Tang, Yan Chen, Zhenrong Yang.   

Abstract

In order to investigate the relationship between sex dysplasia and sex-determining region Y (SRY) gene, 8 patients with sexual abnormality were analyzed by cytogenetic and molecular genetic methods. Fluorescence in situ hybridization (FISH) using PY3.4, X alpha satellite, and SRY probes was performed in each case to analyze the sex chromosome translocation and gene translocation. SRY gene was amplified by polymerase chain reaction (PCR) and its mutation was detected by direct sequencing. The results showed that among 8 patients, 5 were positive for SRY and the remaining negative for SRY. In the patients positive for SRY genes, 3 presented testes and the left 2 streak ovaries. In the patients negative for SRY, only one case presented testes, while 2 ovaries. Direct sequencing demonstrated that all SRY genes were normal in the patients positive for SRY genes. FISH technique demonstrated that SRY genes translocated from Ypter to Xpter in 2 46,XX phenotypic males positive for SRY genes. It was concluded that SRY gene is strongly involved in male sex determination, while a sequence of other genes may be taken into account in sexual development.

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Year:  2004        PMID: 15641705     DOI: 10.1007/BF02831121

Source DB:  PubMed          Journal:  J Huazhong Univ Sci Technolog Med Sci        ISSN: 1672-0733


  9 in total

Review 1.  Sexual differentiation.

Authors:  H Ostrer
Journal:  Semin Reprod Med       Date:  2000       Impact factor: 1.303

Review 2.  The molecular action and regulation of the testis-determining factors, SRY (sex-determining region on the Y chromosome) and SOX9 [SRY-related high-mobility group (HMG) box 9].

Authors:  Vincent R Harley; Michael J Clarkson; Anthony Argentaro
Journal:  Endocr Rev       Date:  2003-08       Impact factor: 19.871

3.  Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation.

Authors:  T Ogata; J R Hawkins; A Taylor; N Matsuo; J Hata; P N Goodfellow
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

Review 4.  An autosomal or X linked mutation results in true hermaphrodites and 46,XX males in the same family.

Authors:  S F Slaney; I J Chalmers; N A Affara; L S Chitty
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

5.  Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene.

Authors:  R Ion; L Telvi; J L Chaussain; J P Barbet; M Nunes; A Safar; M O Réthoré; M Fellous; K McElreavey
Journal:  Hum Genet       Date:  1998-02       Impact factor: 4.132

6.  [46,XY female sex reversal patient with a novel point mutation in the coding sequence of the SRY gene].

Authors:  Chang Zhou; Lu-yun Li; Jun-jiang Fu; Ya-qin Mo; Chang-gao Zhong; Guang-xiu Lu
Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi       Date:  2003-10

7.  Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia.

Authors:  Elisabeth Sock; Roberta A Pagon; Kathelijn Keymolen; Willy Lissens; Michael Wegner; Gerd Scherer
Journal:  Hum Mol Genet       Date:  2003-06-15       Impact factor: 6.150

Review 8.  Gonadoblastoma in a patient with del(9)(p22) and sex reversal: report of a case and review of the literature.

Authors:  Sarantis Livadas; Ariathni Mavrou; Chrystalena Sofocleous; Catherine van Vliet-Constantinidou; Maria Dracopoulou; Catherine Dacou-Voutetakis
Journal:  Cancer Genet Cytogenet       Date:  2003-06

Review 9.  Xp-duplications with and without sex reversal.

Authors:  A Baumstark; G Barbi; M Djalali; C Geerkens; B Mitulla; T Mattfeldt; J C de Almeida; F R Vargas; J C Llerena Júnior; W Vogel; W Just
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

  9 in total

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