Literature DB >> 9070928

Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21.

C Sala1, G Arrigo, G Torri, F Martinazzi, P Riva, L Larizza, C Philippe, P Jonveaux, F Sloan, T Labella, D Toniolo.   

Abstract

Eleven balanced X-autosome translocations associated with premature ovarian failure (POF) were mapped to a YAC contig spanning most of Xq21 and constructed between the DXS223 and DXS1171 loci. The contig corresponds to a genomic region of about 15 Mb and contains the whole X-Y homologous region. The most proximal and most distal breakpoints associated with POF were mapped 15 Mb apart. The remaining breakpoints were localized along this large region, in the X-specific and in the X-Y homologous region. Four of the YACs contained two breakpoints in the same or in flanking STS intervals. Our results confirm the cytological findings and suggest that a minimum number of eight different genes in Xq21 may be involved with ovary development. Interruption of such loci could be the cause of POF.

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Year:  1997        PMID: 9070928     DOI: 10.1006/geno.1996.4542

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  12 in total

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Authors:  Kristel M van Asselt; Helen S Kok; Hein Putter; Cisca Wijmenga; Petra H M Peeters; Yvonne T van der Schouw; Diederick E Grobbee; Egbert R te Velde; Sietse Mosselman; Peter L Pearson
Journal:  Am J Hum Genet       Date:  2004-02-04       Impact factor: 11.025

2.  Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure.

Authors:  Artur Beke; Henriett Piko; Iren Haltrich; Judit Csomor; Andras Matolcsy; György Fekete; Janos Rigo; Veronika Karcagi
Journal:  Mol Cytogenet       Date:  2013-12-20       Impact factor: 2.009

3.  An apparent excess of sex- and reproduction-related genes on the human X chromosome.

Authors:  G M Saifi; H S Chandra
Journal:  Proc Biol Sci       Date:  1999-01-22       Impact factor: 5.349

4.  Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.

Authors:  Arnaud Lacombe; Hane Lee; Laila Zahed; Mahmoud Choucair; Jean-Marc Muller; Stanley F Nelson; Wael Salameh; Eric Vilain
Journal:  Am J Hum Genet       Date:  2006-05-26       Impact factor: 11.025

5.  Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).

Authors:  C R Quilter; A C Karcanias; M R Bagga; S Duncan; A Murray; G S Conway; C A Sargent; N A Affara
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Authors:  M C Hemberger; R S Pearsall; U Zechner; A Orth; S Otto; F Rüschendorf; R Fundele; R Elliott
Journal:  Genetics       Date:  1999-09       Impact factor: 4.562

7.  Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome.

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8.  A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility.

Authors:  S Bione; C Sala; C Manzini; G Arrigo; O Zuffardi; S Banfi; G Borsani; P Jonveaux; C Philippe; M Zuccotti; A Ballabio; D Toniolo
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9.  Chromosomal abnormalities & oxidative stress in women with premature ovarian failure (POF).

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10.  Investigating the role of X chromosome breakpoints in premature ovarian failure.

Authors:  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 Dalprà
Journal:  Mol Cytogenet       Date:  2012-07-16       Impact factor: 2.009

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