Marker-assisted selection for forelimb-girdle muscular anomaly of Japanese Black cattle

被引:5
作者
Masoudi, Ali Akbar
Uchida, Kazuyuki
Yokouchi, Kou
Miyadera, Keiko
Ogawa, Hiroyuki
Sugimoto, Yoshikazu
Kunieda, Tetsuo [1 ]
机构
[1] Okayama Univ, Grad Sch Nat Sci & Technol, Okayama, Japan
[2] Miyazaki Univ, Fac Agr, Miyazaki 88921, Japan
[3] Shirakawa Inst Anim Genet, Fukushima, Japan
[4] Univ Tokyo, Grad Sch Agr & Life Sci, Tokyo, Japan
关键词
carrier; cattle; marker-assisted selection (MAS); muscular anomaly;
D O I
10.1111/j.1740-0929.2007.00489.x
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Forelimb-girdle muscular anomaly is a hereditary disorder of Japanese Black cattle characterized by tremors and astasia caused by hypoplasia of the forelimb-girdle muscles. The locus responsible for this disorder has been mapped on a middle region of bovine chromosome 26. In this study, we applied marker-assisted selection to identify the carriers of this disorder. Four microsatellite markers, DIK4440, BM4505, MOK2602 and IDVGA-59, linked to the disorder locus were genotyped in 37 unaffected offspring of a carrier sire. Transmission of the mutant or wild-type allele of the disorder locus of the sire to the 37 offspring was determined by examining the haplotypes of these markers. The results showed that nine and 18 of the 37 animals possessed the paternally transmitted mutant and wild-type alleles, respectively, and therefore, the nine animals with the mutant allele were identified as carriers. We concluded that the marker-assisted selection using these four markers can be applied for the identification of the carriers of forelimb-girdle muscular anomaly of Japanese Black cattle.
引用
收藏
页码:672 / 675
页数:4
相关论文
共 14 条
[1]   Characterization of human crossover interference [J].
Broman, KW ;
Weber, JL .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (06) :1911-1926
[2]  
Broman KW, 2002, GENETICS, V160, P1123
[3]  
Dekkers J C M, 2004, J Anim Sci, V82 E-Suppl, pE313
[4]   Fine mapping of the polled locus to a 1-Mb region on bovine Chromosome 1q12 [J].
Drögemüller, C ;
Wöhlke, A ;
Mömke, S ;
Distl, O .
MAMMALIAN GENOME, 2005, 16 (08) :613-620
[5]   Estimation of genetic parameters for quantitative trait loci for dairy traits in the French Holstein population [J].
Druet, T. ;
Fritz, S. ;
Boichard, D. ;
Colleau, J. J. .
JOURNAL OF DAIRY SCIENCE, 2006, 89 (10) :4070-4076
[6]   Null mutation of PCLN-1/Claudin-16 results in bovine chronic interstitial nephritis [J].
Hirano, T ;
Kobayashi, N ;
Itoh, T ;
Takasuga, A ;
Nakamaru, T ;
Hirotsune, S ;
Sugimoto, Y .
GENOME RESEARCH, 2000, 10 (05) :659-663
[7]   A comprehensive genetic map of the cattle genome based on 3802 microsatellites [J].
Ihara, N ;
Takasuga, A ;
Mizoshita, K ;
Takeda, H ;
Sugimoto, M ;
Mizoguchi, Y ;
Hirano, T ;
Itoh, T ;
Watanabe, T ;
Reed, KM ;
Snelling, WM ;
Kappes, SM ;
Beattie, CW ;
Bennett, GL ;
Sugimoto, Y .
GENOME RESEARCH, 2004, 14 (10A) :1987-1998
[8]   Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation [J].
Inaba, M ;
Yawata, A ;
Koshino, I ;
Sato, K ;
Takeuchi, M ;
Takakuwa, Y ;
Manno, S ;
Yawata, Y ;
Kanzaki, A ;
Sakai, J ;
Ban, A ;
Ono, K ;
Maede, Y .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (08) :1804-1817
[9]   Identification of genes responsible for hereditary diseases in Japanese beef cattle [J].
Kunieda, Tetsuo .
ANIMAL SCIENCE JOURNAL, 2005, 76 (06) :525-533
[10]  
MASOUDI AA, 2007, UNPUB ANIMAL GENETIC