Cytogenetic and Genetic Studies in a Hypospadic Horse (Equus caballus, 2n=64)

被引:11
作者
De Lorenzi, L. [2 ]
Genualdo, V. [1 ,3 ]
Iannuzzi, A. [4 ]
Di Meo, G. P. [1 ]
Perucatti, A. [1 ]
Mancuso, R.
Russo, M. [5 ]
Di Berardino, D. [4 ]
Parma, P. [2 ]
Iannuzzi, L. [1 ]
机构
[1] CNR, ISPAAM, Lab Anim Cytogenet & Gene Mapping, IT-80147 Naples, Italy
[2] Univ Milan, Dept Anim Prod, Milan, Italy
[3] Univ Bari, Dept Anim Prod, Bari, Italy
[4] Univ Naples Federico II, Dept Soil Plant Environm & Anim Prod Sci, Portici, Italy
[5] Univ Naples Federico II, Sch Vet, Dept Vet Clin Sci, Naples, Italy
关键词
Chromosome deletion; Gene mutation; Horse; Hypospadias; MAMLD1; FISH ANALYSIS; CRYPTORCHIDISM; MUTATIONS;
D O I
10.1159/000319527
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 (C) 2010 S. Karger AG, Basel
引用
收藏
页码:352 / 357
页数:6
相关论文
共 25 条
[1]   MUTATIONS OF THE ANDROGEN RECEPTOR CODING SEQUENCE ARE INFREQUENT IN PATIENTS WITH ISOLATED HYPOSPADIAS [J].
ALLERA, A ;
HERBST, MA ;
GRIFFIN, JE ;
WILSON, JD ;
SCHWEIKERT, HU ;
MCPHAUL, MJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (09) :2697-2699
[2]   11p Microdeletion including WT1 but not PAX6, presenting with cataract, mental retardation, genital abnormalities and seizures: a case report [J].
Almind, Gitte J. ;
Brondum-Nielsen, Karen ;
Bangsgaard, Regitze ;
Baekgaard, Peter ;
Gronskov, Karen .
MOLECULAR CYTOGENETICS, 2009, 2
[3]   Linkage between cryptorchidism, hypospadias, and GGN repeat length in the androgen receptor gene [J].
Aschim, EL ;
Nordenskjöld, A ;
Giwercman, A ;
Lundin, KB ;
Ruhayel, Y ;
Haugen, TB ;
Grotmol, T ;
Giwercman, YL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (10) :5105-5109
[4]   Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity [J].
Halil Aslan ;
Nilay Karaca ;
Seher Basaran ;
Hayri Ermis ;
Yavuz Ceylan .
BMC Pregnancy and Childbirth, 3 (1)
[5]   Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability [J].
Belligni, Elga F. ;
Biamino, Elisa ;
Molinatto, Cristina ;
Messa, Jole ;
Pierluigi, Mauro ;
Faravelli, Francesca ;
Zuffardi, Orsetta ;
Ferrero, Giovanni B. ;
Silengo, Margherita Cirillo .
ITALIAN JOURNAL OF PEDIATRICS, 2009, 35
[6]   Clinical, cytogenetic and hormonal findings in a stallion with hypospadias -: A case report [J].
Bleul, U. ;
Theiss, F. ;
Rutten, M. ;
Kahn, W. .
VETERINARY JOURNAL, 2007, 173 (03) :679-682
[7]   Clinical, cytogenetic and molecular evaluation in a dog with bilateral cryptorchidism and hypospadias [J].
Cassata, R. ;
Iannuzzi, A. ;
Parma, P. ;
De Lorenzi, L. ;
Peretti, V. ;
Perucatti, A. ;
Iannuzzi, L. ;
Di Meo, G. P. .
CYTOGENETIC AND GENOME RESEARCH, 2008, 120 (1-2) :140-143
[8]   The first-generation whole-genome radiation hybrid map in the horse identifies conserved segments in human and mouse genomes [J].
Chowdhary, BP ;
Raudsepp, T ;
Kata, SR ;
Goh, G ;
Millon, LV ;
Allan, V ;
Piumi, F ;
Guérin, G ;
Swinburne, J ;
Binns, M ;
Lear, TL ;
Mickelson, J ;
Murray, J ;
Antczak, DF ;
Womack, JE ;
Skow, LC .
GENOME RESEARCH, 2003, 13 (04) :742-751
[9]   GENE FOR HYPOSPADIAS IN A CHILD WITH PRESUMED TETRASOMY-18P [J].
COTE, GB ;
PETMEZAKI, S ;
BASTAKIS, N .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 4 (02) :141-146
[10]  
Davalieva K, 2009, Prilozi, V30, P57