Literature DB >> 23624391

A novel mutation (c. 341A>G) in the SRY gene in a 46,XY female patient with gonadal dysgenesis.

Zofia Helszer1, Anita Dmochowska, Janusz Szemraj, Jolanta Słowikowska-Hilczer, Marek Wieczorek, Sławomir Jędrzejczyk, Bogdan Kałużewski.   

Abstract

SRY (sex-determining region Y) gene, MIM 480000, NM_005634) is crucial for sex differentiation which encodes the protein responsible for initiating testis differentiation. SRY mutations are associated with the presence of XY gonadal dysgenesis symptoms. We studied a 46,XY female patient with primary amenorrhoea and negative family history. The clinical, endocrine, histopathologic and cytogenetic data are consistent with gonadal dysgenesis. Using a molecular analysis, a novel (c.341A>G, p. N65D) missense mutation within the HMGbox of SRY gene was detected. Escherichia coli expression of SRY study showed reduced expression of the mutated protein and gel retardation assay method revealed lowered DNA-binding ability in N65D variant of SRY. The novel mutation detected in the SRY gene may be an aetiopathogenic factor in clinically defined 46,XY complete gonadal dysgenesis (CGD). Because of an increased risk of gonadoblastoma, proper early diagnosis and treatment prevent development of malignancies.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CGD; Complete Gonadal Dysgenesis; DSD; Disorder of Sex Development; Disorder of sex development; HMG; HMG-box; High Mobility Group; Missense mutation; NLS; NR5A1; NROB1; Nuclear Localization Signal; R-spondin 1; RSPO1; SOX9; SRY; SRY (sex determining region Y)-box 9; SRY gene; Sex-determining Region of Y chromosome; WNT4; WT1; Wilms tumor 1; nuclear receptor subfamily 0, group B, member 1; nuclear receptor subfamily 5, group A, member 1; wingless-type MMTV integration site family, member 4

Mesh:

Year:  2013        PMID: 23624391     DOI: 10.1016/j.gene.2013.04.027

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  5 in total

1.  A rare cause of primary amenorrhoea, the XY female with gonadal dysgenesis.

Authors:  Dominique Mannaerts; Joke Muys; Bettina Blaumeiser; Yves Jacquemyn
Journal:  BMJ Case Rep       Date:  2015-02-09

Review 2.  New insights into the genetic basis of infertility.

Authors:  Thejaswini Venkatesh; Padmanaban S Suresh; Rie Tsutsumi
Journal:  Appl Clin Genet       Date:  2014-12-01

3.  The Evaluation of Cases with Y-Chromosome Gonadal Dysgenesis: Clinical Experience over 18 Years.

Authors:  Merih Berberoğlu; Zeynep Şıklar
Journal:  J Clin Res Pediatr Endocrinol       Date:  2017-08-21

4.  Cellular fate of intersex differentiation.

Authors:  Xin Wang; Fengling Lai; Dantong Shang; Yibin Cheng; Tian Lan; Hanhua Cheng; Rongjia Zhou
Journal:  Cell Death Dis       Date:  2021-04-12       Impact factor: 8.469

5.  A case report of 46,XY partial gonadal dysgenesis caused by a novel mutation in the sex-determining region gene.

Authors:  Ke Xu; Na Su; Hong Zhang; Jingxin Zhu; Xinran Cheng
Journal:  Transl Pediatr       Date:  2020-12
  5 in total

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