Association analysis of adiponectin and somatostatin polymorphisms on BTA1 with growth and carcass traits in Angus cattle

被引:58
作者
Morsci, N. S. [1 ]
Schnabel, R. D. [1 ]
Taylor, J. F. [1 ]
机构
[1] Univ Missouri, Div Anim Sci, Columbia, MO 65211 USA
关键词
adiponectin; Angus; association; beef; carcass traits; linkage disequilibrium; quantitative trait loci; single nucleotide polymorphism; somatostatin;
D O I
10.1111/j.1365-2052.2006.01528.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
This study tested positional candidate genes adiponectin (ADIPOQ) and somatostatin (SST) for effects on carcass traits in a commercially relevant cattle population. Both genes are located within a region of BTA1 previously reported to harbour quantitative trait loci (QTL) that affect marbling, quality grade, yield grade, ribeye area and weaning weight in Bos taurus x Bos indicus crosses. Except for the first intron of ADIPOQ, both genes, including over 2 kb upstream of the promoters, were sequenced in five registered Angus sires to identify polymorphisms. A variable copy duplication and three single nucleotide polymorphisms (SNPs) in ADIPOQ and one SNP in SST were genotyped and tested for association with 19 traits in a 14-generation pedigree of 1697 registered Angus artificial insemination sires representing all the major USA lineages of the breed. Linear models that parameterized predicted genetic merits in terms of allele substitution effects were fit by weighted least squares, and goodness-of-fit tests were employed to differentiate causal mutations or polymorphisms in strong linkage disequilibrium (LD) with causal mutations from markers in weak LD with QTL. We confirmed the presence of QTL affecting marbling, ribeye muscle area and fat thickness in the vicinity of SST and ADIPOQ on BTA1 in Angus; excluded SST as underlying the ribeye muscle area QTL; and excluded ADIPOQ as underlying the marbling score QTL. However, association analysis provides very limited information about QTL location and has little intrinsic value when performed in the absence of linkage or LD analysis using flanking marker data to localize the QTL effect relative to positional candidate genes.
引用
收藏
页码:554 / 562
页数:9
相关论文
共 39 条
[1]   Myocyte enhancer factor-2 and serum response factor binding elements regulate fast myosin heavy chain transcription in vivo [J].
Allen, DL ;
Weber, JN ;
Sycuro, LK ;
Leinwand, LA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) :17126-17134
[2]   Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Takahashi, M ;
Maeda, K ;
Miyagawa, J ;
Hotta, K ;
Shimomura, I ;
Nakamura, T ;
Miyaoka, K ;
Kuriyama, H ;
Nishida, M ;
Yamashita, S ;
Okubo, K ;
Matsubara, K ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) :79-83
[3]   Adiponectin and its receptors are expressed in bone-forming cells [J].
Berner, HS ;
Lyngstadaas, SP ;
Spahr, A ;
Monjo, M ;
Thommesen, L ;
Drevon, CA ;
Syversen, U ;
Reseland, JE .
BONE, 2004, 35 (04) :842-849
[4]   Hepatic lipase promoter activity is reduced by the C-480T and G-216A substitutions present in the common LIPC gene variant, and is increased by Upstream Stimulatory Factor [J].
Botma, GJ ;
Verhoeven, AJM ;
Jansen, H .
ATHEROSCLEROSIS, 2001, 154 (03) :625-632
[5]  
Bullock KD, 2000, J ANIM SCI, V78, P2540
[6]  
Cai L, 2004, United States Patent Application, Patent No. 20040018511
[7]   Essential role in vivo of upstream stimulatory factors for a normal dietary response of the fatty acid synthase gene in the liver [J].
Casado, M ;
Vallet, VS ;
Kahn, A ;
Vaulont, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2009-2013
[8]   Adiponectin: More than just another fat cell hormone? [J].
Chandran, M ;
Phillips, SA ;
Ciaraldi, T ;
Henry, RR .
DIABETES CARE, 2003, 26 (08) :2442-2450
[9]   The role of the novel adipocyte-derived hormone adiponectin in human disease [J].
Díez, JJ ;
Iglesias, P .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2003, 148 (03) :293-300
[10]   EFFECTS OF PHYSIOLOGIC LEVELS OF GLUCAGON AND GROWTH-HORMONE ON HUMAN CARBOHYDRATE AND LIPID-METABOLISM - STUDIES INVOLVING ADMINISTRATION OF EXOGENOUS HORMONE DURING SUPPRESSION OF ENDOGENOUS HORMONE-SECRETION WITH SOMATOSTATIN [J].
GERICH, JE ;
LORENZI, M ;
BIER, DM ;
TSALIKIAN, E ;
SCHNEIDER, V ;
KARAM, JH ;
FORSHAM, PH .
JOURNAL OF CLINICAL INVESTIGATION, 1976, 57 (04) :875-884