The locus for bovine dilated cardiomyopathy maps to chromosome 18

被引:6
作者
Guziewicz, K. E.
Owczarek-Lipska, M.
Kueffer, J.
Schelling, C.
Tontis, A.
Denis, C.
Eggen, A.
Leeb, T.
Dolf, G.
Braunschweig, M. H. [1 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Clin Studies, Philadelphia, PA 19104 USA
[2] Univ Bern, Vetsuisse Fac, Inst Genet, CH-3001 Bern, Switzerland
[3] Univ Zurich, Vetsuisse Fac, Clin Lab, CH-8092 Zurich, Switzerland
[4] Univ Bern, Vetsuisse FAc, Inst Anim Pathol, Bern, Switzerland
[5] INRA, Dept Anim Genet, Lab Biochem Genet & Cytogenet, F-78350 Jouy En Josas, France
关键词
bovine dilated cardiomyopathy; BTA18; genome scan; TNN13;
D O I
10.1111/j.1365-2052.2007.01596.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
Bovine dilated cardiomyopathy (BDCMP) is a severe and terminal disease of the heart muscle observed in Holstein - Friesian cattle over the last 30 years. There is strong evidence for an autosomal recessive mode of inheritance for BDCMP. The objective of this study was to genetically map BDCMP, with the ultimate goal of identifying the causative mutation. A whole-genome scan using 199 microsatellite markers and one SNP revealed an assignment of BDCMP to BTA18. Fine-mapping on BTA18 refined the candidate region to the MSBDCMP06-BMS2785 interval. The interval containing the BDCMP locus was confirmed by multipoint linkage analysis using the software LOKI. The interval is about 6.7 Mb on the bovine genome sequence (Btau 3.1). The corresponding region of HSA19 is very gene-rich and contains roughly 200 genes. Although telomeric of the marker interval, TNNI3 is a possible positional and a functional candidate for BDCMP given its involvement in a human form of dilated cardiomyopathy. Sequence analysis of TNNI3 in cattle revealed no mutation in the coding sequence, but there was a G-to-A transition in intron 6 (AJ842179: c. 378+ 315G > A). The analysis of this SNP using the study's BDCMP pedigree did not conclusively exclude TNNI3 as a candidate gene for BDCMP. Considering the high density of genes on the homologous region of HSA19, further refinement of the interval on BTA18 containing the BDCMP locus is needed.
引用
收藏
页码:265 / 269
页数:5
相关论文
共 24 条
[1]   A SIMPLE AND EFFICIENT METHOD FOR ISOLATING HIGH MOLECULAR-WEIGHT DNA FROM MAMMALIAN SPERM [J].
BAHNAK, BR ;
WU, QY ;
COULOMBEL, L ;
DROUET, L ;
KERBIRIOUNABIAS, D ;
MEYER, D .
NUCLEIC ACIDS RESEARCH, 1988, 16 (03) :1208-1208
[2]  
Baird J. D., 1986, Proceedings of the 14th World Congress on Diseases of Cattle, Dublin, V1, P89
[3]   CARDIOMYOPATHY IN ADULT HOLSTEIN FRIESIAN CATTLE IN BRITAIN [J].
BRADLEY, R ;
JEFFERIES, AR ;
JACKSON, PGG ;
WIJERATNE, WVS .
JOURNAL OF COMPARATIVE PATHOLOGY, 1991, 104 (01) :101-112
[4]  
COTTINGHAM RW, 1993, AM J HUM GENET, V53, P252
[5]  
DANZL H, 1995, WIEN TIERARZTL MONAT, V82, P16
[6]  
Dolf G, 1998, J ANIM SCI, V76, P1824
[7]  
Eggen A, 2001, GENET SEL EVOL, V33, P543, DOI 10.1051/gse:2001132
[8]   DIAGNOSIS OF BOVINE CARDIOMYOPATHY BY ELECTROLYTE AND PROTEIN-ANALYSIS [J].
GRABER, HU ;
MARTIG, J .
JOURNAL OF VETERINARY MEDICINE SERIES A-ZENTRALBLATT FUR VETERINARMEDIZIN REIHE A-PHYSIOLOGY PATHOLOGY CLINICAL MEDICINE, 1993, 40 (9-10) :690-696
[9]  
Green P., 1990, DOCUMENTATION CRIMAP
[10]   Markov chain Monte Carlo segregation and linkage analysis for oligogenic models [J].
Heath, SC .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (03) :748-760