Investigating the role of X chromosome breakpoints in premature ovarian failure

Simona Baronchelli, Nicoletta Villa, Serena Redaelli, Sara Lissoni, Fabiana Saccheri, Elena Panzeri, Donatella Conconi, Angela Bentivegna, Francesca Crosti, Elena Sala, Francesca Bertola, Anna Marozzi, Antonio Pedicini, Marialuisa Ventruto, Maria Adalgisa Police, Leda Dalprá

Research output: Contribution to journalArticle

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Abstract

The importance of the genetic factor in the aetiology of premature ovarian failure (POF) is emphasized by the high percentage of familial cases and X chromosome abnormalities account for 10% of chromosomal aberrations. In this study, we report the detailed analysis of 4 chromosomal abnormalities involving the X chromosome and associated with POF that were detected during a screening of 269 affected women. Conventional and molecular cytogenetics were valuable tools for locating the breakpoint regions and thus the following karyotypes were defined: 46,X,der(X)t (X;19)(p21.1;q13.42)mat, 46,X,t(X;2)(q21.33;q14.3)dn, 46,X,der(X)t(X;Y)(q26.2;q11.223)mat and 46,X,t(X;13)(q13.3;q31)dn. A bioinformatic analysis of the breakpoint regions identified putative candidate genes for ovarian failure near the breakpoint regions on the X chromosome or on autosomes that were involved in the translocation event. HS6ST1, HS6ST2 and MATER genes were identified and their functions and a literature review revealed an interesting connection to the POF phenotype. Moreover, the 19q13.32 locus is associated with the age of onset of the natural menopause. These results support the position effect of the breakpoint on flanking genes, and cytogenetic techniques, in combination with bioinformatic analysis, may help to improve what is known about this puzzling disorder and its diagnostic potential.

Original languageEnglish
Article number32
JournalMolecular Cytogenetics
Volume5
Issue number1
DOIs
Publication statusPublished - 2012

Fingerprint

Chromosome Breakpoints
Primary Ovarian Insufficiency
X Chromosome
Chromosomes
Chromosome Aberrations
Genes
Bioinformatics
Computational Biology
Cytogenetic Analysis
Menopause
Aberrations
Karyotype
Age of Onset
Cytogenetics
Screening
Phenotype

Keywords

  • Breakpoint definition
  • Premature ovarian failure
  • X chromosome structural aberrations

ASJC Scopus subject areas

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

Cite this

Baronchelli, S., Villa, N., Redaelli, S., Lissoni, S., Saccheri, F., Panzeri, E., ... Dalprá, L. (2012). Investigating the role of X chromosome breakpoints in premature ovarian failure. Molecular Cytogenetics, 5(1), [32]. https://doi.org/10.1186/1755-8166-5-32

Investigating the role of X chromosome breakpoints in premature ovarian failure. / Baronchelli, Simona; Villa, Nicoletta; Redaelli, Serena; Lissoni, Sara; Saccheri, Fabiana; Panzeri, Elena; Conconi, Donatella; Bentivegna, Angela; Crosti, Francesca; Sala, Elena; Bertola, Francesca; Marozzi, Anna; Pedicini, Antonio; Ventruto, Marialuisa; Police, Maria Adalgisa; Dalprá, Leda.

In: Molecular Cytogenetics, Vol. 5, No. 1, 32, 2012.

Research output: Contribution to journalArticle

Baronchelli, S, Villa, N, Redaelli, S, Lissoni, S, Saccheri, F, Panzeri, E, Conconi, D, Bentivegna, A, Crosti, F, Sala, E, Bertola, F, Marozzi, A, Pedicini, A, Ventruto, M, Police, MA & Dalprá, L 2012, 'Investigating the role of X chromosome breakpoints in premature ovarian failure', Molecular Cytogenetics, vol. 5, no. 1, 32. https://doi.org/10.1186/1755-8166-5-32
Baronchelli, Simona ; Villa, Nicoletta ; Redaelli, Serena ; Lissoni, Sara ; Saccheri, Fabiana ; Panzeri, Elena ; Conconi, Donatella ; Bentivegna, Angela ; Crosti, Francesca ; Sala, Elena ; Bertola, Francesca ; Marozzi, Anna ; Pedicini, Antonio ; Ventruto, Marialuisa ; Police, Maria Adalgisa ; Dalprá, Leda. / Investigating the role of X chromosome breakpoints in premature ovarian failure. In: Molecular Cytogenetics. 2012 ; Vol. 5, No. 1.
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