Kadarmideen Haja N, Janss Luc L G
Animal Sciences Group, Wageningen University and Research Centre, 8200 AB Lelystad, The Netherlands.
Genetics. 2005 Nov;171(3):1195-206. doi: 10.1534/genetics.105.040956. Epub 2005 Jul 14.
Bayesian segregation analyses were used to investigate the mode of inheritance of osteochondral lesions (osteochondrosis, OC) in pigs. Data consisted of 1163 animals with OC and their pedigrees included 2891 animals. Mixed-inheritance threshold models (MITM) and several variants of MITM, in conjunction with Markov chain Monte Carlo methods, were developed for the analysis of these (categorical) data. Results showed major genes with significant and substantially higher variances (range 1.384-37.81), compared to the polygenic variance (sigmau2). Consequently, heritabilities for a mixed inheritance (range 0.65-0.90) were much higher than the heritabilities from the polygenes. Disease allele frequencies range was 0.38-0.88. Additional analyses estimating the transmission probabilities of the major gene showed clear evidence for Mendelian segregation of a major gene affecting osteochondrosis. The variants, MITM with informative prior on sigmau2, showed significant improvement in marginal distributions and accuracy of parameters. MITM with a "reduced polygenic model" for parameterization of polygenic effects avoided convergence problems and poor mixing encountered in an "individual polygenic model." In all cases, "shrinkage estimators" for fixed effects avoided unidentifiability for these parameters. The mixed-inheritance linear model (MILM) was also applied to all OC lesions and compared with the MITM. This is the first study to report evidence of major genes for osteochondral lesions in pigs; these results may also form a basis for underpinning the genetic inheritance of this disease in other animals as well as in humans.
采用贝叶斯分离分析方法研究猪骨软骨损伤(骨软骨病,OC)的遗传模式。数据包括1163只患有OC的动物,其谱系包含2891只动物。为分析这些(分类)数据,开发了混合遗传阈值模型(MITM)及其几种变体,并结合马尔可夫链蒙特卡罗方法。结果显示,与多基因方差(sigmau2)相比,主基因具有显著且更高的方差(范围为1.384 - 37.81)。因此,混合遗传的遗传力(范围为0.65 - 0.90)远高于多基因的遗传力。疾病等位基因频率范围为0.38 - 0.88。估计主基因传递概率的进一步分析表明,有明确证据支持影响骨软骨病的主基因的孟德尔分离。在sigmau2上具有信息先验的MITM变体在边际分布和参数准确性方面有显著改善。采用“简化多基因模型”对多基因效应进行参数化的MITM避免了“个体多基因模型”中遇到的收敛问题和混合不佳的情况。在所有情况下,固定效应的“收缩估计器”避免了这些参数的不可识别性。混合遗传线性模型(MILM)也应用于所有OC损伤,并与MITM进行比较。这是首次报道猪骨软骨损伤主基因证据的研究;这些结果也可能为其他动物以及人类该疾病的遗传继承研究奠定基础。