Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure

Artur Beke, Henriett Piko, Iren Haltrich, Judit Csomor, Andras Matolcsy, György Fekete, Janos Rigo, Veronika Karcagi

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Background: One of the frequent reasons for unsuccessful conception is premature ovarian failure/primary ovarian insufficiency (POF/POI) that is defined as the loss of functional follicles below the age of 40 years. Among the genetic causes the most common one involves the X chromosome, as in Turner syndrome, partial X deletion and X-autosome translocations. Here we report a case of a 27-year-old female patient referred to genetic counselling because of premature ovarian failure. The aim of this case study to perform molecular genetic and cytogenetic analyses in order to identify the exact genetic background of the pathogenic phenotype. Results: For premature ovarian failure disease diagnostics we performed the Fragile mental retardation 1 gene analysis using Southern blot technique and Repeat Primed PCR in order to identify the relationship between the Fragile mental retardation 1 gene premutation status and the premature ovarion failure disease. At this early onset, the premature ovarian failure affected patient we detected one normal allele of Fragile mental retardation 1 gene and we couldn't verify the methylated allele, therefore we performed the cytogenetic analyses using G-banding and fluorescent in situ hybridization methods and a high resolution molecular cytogenetic method, the array comparative genomic hybridization technique. For this patient applying the G-banding, we identified a large deletion on the X chromosome at the critical region (ChrX q21.31-q28) which is associated with the premature ovarian failure phenotype. In order to detect the exact breakpoints, we used a special cytogenetic array ISCA plus CGH array and we verified a 67.355 Mb size loss at the critical region which include total 795 genes. Conclusions: We conclude for this case study that the karyotyping is definitely helpful in the evaluation of premature ovarian failure patients, to identify the non submicroscopic chromosomal rearrangement, and using the array CGH technique we can contribute to the most efficient detection and mapping of exact deletion breakpoints of the deleted Xq region.

Original languageEnglish
Article number62
JournalMolecular Cytogenetics
Volume6
Issue number1
DOIs
Publication statusPublished - Dec 20 2013

Keywords

  • Array-comparative genomic hybridization (aCGH)
  • Deletion breakpoint
  • FMR1 gene analysis
  • G-banding
  • Premature premature ovarian failure (POF)
  • Primary ovarian insufficiency (POI)
  • Repeat primed PCR
  • Sterility
  • Turner syndrome
  • X chromosome deletion

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Genetics
  • Genetics(clinical)
  • Biochemistry, medical

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