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中国西门塔尔牛MC3R和MC4R基因组织表达谱及其在脂肪组织中表达水平与背膘厚度的相关性研究 被引量:19

The Tissues Profile of MC3R and MC4R and the Association of Their Expression in the Adipose with Backfat Thickness in Chinese Simmental Cattle
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摘要 为探索调控肉牛脂肪沉积的关键基因表达规律,筛选影响肉牛肥育性状的候选基因,本研究采用137头18月龄肉用中国西门塔尔公牛,屠宰并采集组织样品,根据背膘厚度胴体测定值分成高、低2组,每组各选择15个个体,利用荧光实时定量技术对MC3R和MC4R基因在组织中的表达特征及其在不同个体脂肪组织中的表达水平进行分析。结果表明,MC3R和MC4R基因在睾丸、小肠、心脏、胰腺、淋巴、肾脏、脾脏、肝脏、肺脏、肌肉和脂肪组织中均有不同程度的表达,MC3R和MC4R基因在不同组之间的表达差异显著(P<0.05),且与背膘厚度呈显著相关(r=0.784,P<0.05;r=0.836,P<0.05)。结果说明MC3R和MC4R基因与肉牛背膘厚度有显著相关,是影响肉牛肥育性状的候选基因。 In order to explore the expression rule of key gene and screen the candidate gene affecting fat deposition,30 samples from 137 slaughtered 18 month Chinese simmental beef cattle were divided into thick(H) and thin(L) backfat groups,and the expression of MC3R and MC4R were analyzed in the adipose of different samples and other tissues.The result indicated that both the MC3R and MC4R expressed in the heart,liver,spleen,lung,kidney,muscle,adipose,thymus,small intestine,lymph and testis.The abundances of both the MC3R and MC4R mRNA in adipose were higher in L group than those in H group(P0.05),and correlated with backfat thickness(r=0.784,P0.05;r=0.836,P0.05;respectively).The results indicate that MC3R and MC4R had significant relationship with backfat thickness and might be a candidate gene for fattening in beef cattle.
出处 《畜牧兽医学报》 CAS CSCD 北大核心 2011年第4期489-494,共6页 ACTA VETERINARIA ET ZOOTECHNICA SINICA
基金 国家转基因新品种重大专项(2008ZX08007-002 2009ZX08009-157B)
关键词 肉牛 MC3R MC4R 表达谱 脂肪沉积 beef cattle MC3R MC4R expression profile fat deposition
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参考文献24

  • 1KONDA Y, GANTZ I, DELVALLE J, et al. Interaction of dual intracellular signaling pathways activated by the melanocortin-3 receptor [J]. Biol Chem, 1994, 269(18):13162-13166.
  • 2BUTLER A A, KESTERSON R A, KHONG K, et al. A unique metabolic syndrome causes obesity in the melanocortin-3 receptor deficient mouse [J]. Endo- crinology, 2000, 141(9): 3518-3521.
  • 3CHEN A S, MARSH D J, TRUMBAUER M E, et al. Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass [J]. NatGenet, 2000, 26(1): 97-102.
  • 4LI W D, JOO E J, FURBURG E B, et al. Melanocortin 3 receptor (MC3R) gene variants in extremely obese women [J]. Int J Relat Metah Disord, 2000, 24(2) : 206-210.
  • 5TAKEUCHI S, TAKAHASHI S. A possible involvement of melanocortin 3 receptor in the regulation of adrenal gland functions in the chicken [J]. Biochem Biophys Asta, 1999, 1448(3) : 512-518.
  • 6蒋思文,JACOBSSON Lina,KERJE Susanne,ANDERSSON Leif,熊远著.参考家系鸡黑素皮质素受体3基因多态性与体重关系研究[J].Acta Genetica Sinica,2002,29(4):322-325. 被引量:24
  • 7CHEN H, CHARLAT O, TARTAGLIA L A, et al. Evidence that the diabetes gene encodes the Leptinreceptor: identification of a mutation in the Leptin receptorgene in db/db mice[J].Cell, 1996,84: 491- 495.
  • 8SATOH N,OGAWA Y,KATSUIRA G, et al. Satiety effect and sympathetic activation of Leptin are mediated by hypothalamic melanocortin system [J]. Neurosci Lett, 1998,249 : 107-110.
  • 9MARIE L, MIURA G L, MARSH D J,et al. A metabolie defect promotes obesity in mice lacking melanocortin- 4 receptors [J]. Proc Natl Acad Sci, 2000,97: 12339-12344.
  • 10KIM K S, LARSEN N J, ROTHSCHILD M F. Rapid communication linkage and physical mapping of the porcine melanoeortin-4 receptor (MC4R) gene [J]. Anim Sci, 2000, 78(3): 791-792.

二级参考文献24

  • 1[1]Woods S C et al. Signals that regulate food intake and energy homeostasis. Science, 1998,280(5368):1378~1383.
  • 2[2]Cone R D. The Central Melanocortin System and Energy Homeostasis. Trends Endocrinol Metab., 1999,10(6):211~216.
  • 3[3]Yeo G S, Farooqi I S, Challis B G, Jackson R S, O'Rahilly S. The role of melanocortin signalling in the control of body weight:evidence from human and murine genetic models. QJM, 2000,93(1):7~14.
  • 4[4]Barsh G S, Farooqi I S, O'Rahilly S. Genetics of body-weight regulation. Nature, 2000,404(6778):644~651.
  • 5[5]Schwartz M W et al. Central nervous system control of food intake. Nature, 2000,404(6778):661~671.
  • 6[6]Huszar D, Lynch C A, Fairchild-Huntress V et al. Targeted disruption of the melanocortin-4 receptor results in obesity in mice. Cell, 1997,88(1):131~141.
  • 7[7]Yeo G S, Farooqi I S, Aminian S, Halsall D J, Stanhope R G, O'Rahilly S. A frame-shift mutation in MC4R associated with dominantly inherited human obesity. Nat.Genet., 1998,20(2):111~112.
  • 8[8]Vaisse C, Clement K, Guy-Grand B, Froguel P. A frameshift mutation in human MC4R is associated with a dominant form of obesity. Nat.Genet., 1998,20(2):113~114.
  • 9[9]Butler A A, Kesterson R A, Khong K, Cullen M J, Pelleymounter M A, Dekoning J, Baetscher M, Cone R D. A unique metabolic syndrome causes obesity in the melanocortin-3 receptor-deficient mouse. Endocrinology, 2000,141(9):3518~3521.
  • 10[10]Chen A S, Marsh D J, Trumbauer M E et al. Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass. Nat.Genet., 2000,26(1):97~102.

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