HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Identification of a novel mutation (Ala66Thr) of SRY gene causes XY pure gonadal dysgenesis by affecting DNA binding activity and nuclear import.

Abstract
Sex-determining region of the Y chromosome (SRY) gene plays a crucial role in male sexual differentiation and development. Several mutations in the SRY gene have been reported in the high mobility group (HMG) box domain and can cause gonadal dysgenesis symptoms. In this study, we report that a novel missense mutation in the SRY gene, a G to A transition within the HMG box, causes the Ala66Thr amino acid substitution in a female patient presenting 46,XY karyotype with pure gonadal dysgenesis. The G to A base transition was not found in the SRY sequence after the screening of 100 normal males. Furthermore, Ala66Thr mutation drastically reduced the binding capacity of SRY to DNA sequences, whereas wild-type SRY protein showed the normal binding capacity to DNA sequences in vitro. We also found that the mutant SRY protein was partly localized in cytoplasm, whereas wild-type SRY protein was strictly localized in cell nucleus. In addition, we analyzed the three-dimensional structure of SRY protein by homology modeling methods. In conclusion, we identified a novel SRY mutation in a 46,XY female patient with pure gonadal dysgenesis, demonstrating the importance of the Ala66Thr mutation in DNA binding activity and nuclear transport.
AuthorsXiang Wang, Mei Xue, Minggang Zhao, Fang He, Cui Li, Xu Li
JournalGene (Gene) Vol. 651 Pg. 143-151 (Apr 20 2018) ISSN: 1879-0038 [Electronic] Netherlands
PMID29378242 (Publication Type: Case Reports, Journal Article)
CopyrightCopyright © 2018 Elsevier B.V. All rights reserved.
Chemical References
  • Sex-Determining Region Y Protein
  • Threonine
  • DNA
  • Alanine
Topics
  • Active Transport, Cell Nucleus
  • Adolescent
  • Adult
  • Alanine
  • DNA (metabolism)
  • Female
  • Gonadal Dysgenesis, 46,XY (genetics)
  • HEK293 Cells
  • Humans
  • Karyotyping
  • Male
  • Mutation, Missense
  • Protein Binding
  • Protein Conformation
  • Sequence Analysis, DNA
  • Sex-Determining Region Y Protein (chemistry, genetics, metabolism)
  • Threonine
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: