Literature DB >> 20733278

Cytogenetic and genetic studies in a hypospadic horse (Equus caballus, 2n = 64).

L De Lorenzi1, V Genualdo, A Iannuzzi, G P Di Meo, A Perucatti, R Mancuso, M Russo, D Di Berardino, P Parma, Leopoldo Iannuzzi.   

Abstract

A 4-year-old male horse of Friesian breed with normal body conformation, development and libido, and showing an evident ventral penis deviation with hypospadias, underwent both cytogenetic and genetic investigation. Although the karyotype showed normal male arrangement (2n = 64,XY), one telomere of horse (ECA) chromosome 1 was shorter than both the other one and those of a normal horse (control), as revealed by CBA- and RBA-banding, and by Ag-NOR and FISH-mapping techniques using telomere PNA probes. Genetic investigation of the SRY and MAMLD1 coding sequences revealed a normal SRY sequence and a mutation in the MAMLD1 gene sequence: a homozygous change (C>A) was found, leading to the synthesis of an isoleucine, instead of a leucine. Although it is difficult to find a strict correlation between hypospadias and the genetic defects revealed by this investigation, this study is the first to be performed in a hypospadic horse using both cytogenetic and genetic investigation.
Copyright © 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 20733278     DOI: 10.1159/000319527

Source DB:  PubMed          Journal:  Sex Dev        ISSN: 1661-5425            Impact factor:   1.824


  3 in total

Review 1.  The Genetic and Environmental Factors Underlying Hypospadias.

Authors:  Aurore Bouty; Katie L Ayers; Andrew Pask; Yves Heloury; Andrew H Sinclair
Journal:  Sex Dev       Date:  2015-11-28       Impact factor: 1.824

2.  Clinical, cytogenetic and molecular genetic characterization of a tandem fusion translocation in a male Holstein cattle with congenital hypospadias and a ventricular septal defect.

Authors:  Alessandra Iannuzzi; Marina Braun; Viviana Genualdo; Angela Perucatti; Sina Reinartz; Ioannis Proios; Maike Heppelmann; Jürgen Rehage; Kirsten Hülskötter; Andreas Beineke; Julia Metzger; Ottmar Distl
Journal:  PLoS One       Date:  2020-01-10       Impact factor: 3.240

3.  Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype.

Authors:  Núria Camats; Mónica Fernández-Cancio; Laura Audí; Primus E Mullis; Francisca Moreno; Isabel González Casado; Juan Pedro López-Siguero; Raquel Corripio; José Antonio Bermúdez de la Vega; José Antonio Blanco; Christa E Flück
Journal:  PLoS One       Date:  2015-11-16       Impact factor: 3.240

  3 in total

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