Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism

Lawrence C Layman, Sae H. Sohn, Douglas B. Peak, Richard H. Reindollar, Jun Xie, Mark R. Gray

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Objective: To determine if GnRH receptor mutations occur in patients with idiopathic hypogonadotropic hypogonadism. Design: Patients and controls were studied by molecular genetic analysis. Setting. A tertiary medical center setting. Patient(s): Twenty-four patients with idiopathic hypogonadotropic hypogonadism and 20 controls. Intervention(s): Deoxyribonucleic acid from all individuals was analyzed by Southern blot analysis and denaturing gradient gel electrophoresis. Genomic DNA was digested with restriction enzymes, and Southern blots and denaturing gradient gel blots were constructed. Blots were hybridized with the GnRH receptor complementary DNA probe. The DNA sequencing was performed on samples from two representative patients. Main Outcome Measure(s): Gonadotropin-releasing hormone receptor gene structure was ascertained by comparing fragments from autoradiographs in patients and controls. Individual nucleotides were ascertained from DNA sequencing gels. Result(s): No GnRH receptor gene deletions or polymorphisms were identified by Southern blot analysis. New restriction-fragment melting polymorphisms using the enzymes DpnII, RsaI, and HaeIII were identified by denaturing gradient gel blots in patients and controls. Conclusion(s): Gonadotropin-releasing hormone receptor gene deletions or rearrangements were not observed in our idiopathic hypogonadotropic hypogonadism patients. Denaturing gradient gel electrophoresis failed to identify single-base differences unique to patients with idiopathic hypogonadotropic hypogonadism, dramatically reducing the likelihood that point mutations of the GnRH receptor gene are present in idiopathic hypogonadotropic hypogonadism.

Original languageEnglish (US)
Pages (from-to)1079-1085
Number of pages7
JournalFertility and sterility
Volume68
Issue number6
DOIs
StatePublished - Dec 1 1997
Externally publishedYes

Fingerprint

LHRH Receptors
Mutation
Genes
Southern Blotting
Denaturing Gradient Gel Electrophoresis
Gels
Gene Deletion
DNA Sequence Analysis
Patient Advocacy
Idiopathic Hypogonadotropic Hypogonadism
Gene Rearrangement
DNA
DNA Probes
Enzymes
Point Mutation
Freezing
Molecular Biology
Nucleotides
Complementary DNA
Outcome Assessment (Health Care)

Keywords

  • GnRH deficiency
  • GnRH receptor
  • Idiopathic hypogonadotropic hypogonadism
  • Kallmann syndrome

ASJC Scopus subject areas

  • Reproductive Medicine
  • Obstetrics and Gynecology

Cite this

Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism. / Layman, Lawrence C; Sohn, Sae H.; Peak, Douglas B.; Reindollar, Richard H.; Xie, Jun; Gray, Mark R.

In: Fertility and sterility, Vol. 68, No. 6, 01.12.1997, p. 1079-1085.

Research output: Contribution to journalArticle

Layman, Lawrence C ; Sohn, Sae H. ; Peak, Douglas B. ; Reindollar, Richard H. ; Xie, Jun ; Gray, Mark R. / Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism. In: Fertility and sterility. 1997 ; Vol. 68, No. 6. pp. 1079-1085.
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