A finite locus model to estimate additive variance and the breeding values
was implemented using Gibbs sampling. Four different distributions for the
size of the gene effects across the loci were considered: i) uniform with l
oci of different effects, ii) uniform with all loci having equal effects, i
ii) exponential, and iv) normal. Stochastic simulation was used to study th
e influence of the number of loci and the distribution of their effect assu
med in the model analysis. The assumption of loci with different and unifor
mly distributed effects resulted in an increase in the estimate of the addi
tive variance according to the number of loci assumed in the model of analy
sis, causing biases in the estimated breeding values. When the gene effects
were assumed to be exponentially distributed, the estimate of the additive
variance was still dependent on the number of loci assumed in the model of
analysis, but this influence was much less. When assuming that all the loc
i have the same gene effects or when they were normally distributed, the ad
ditive variance estimate was the same regardless of the number of loci assu
med in the model of analysis. The estimates were not significantly differen
t from either the true simulated values or from those obtained when using t
he standard mixed model approach where an infinitesimal model is assumed. T
he results indicate that if the number of loci has to be assumed a priori,
the most useful finite locus models are those assuming loci with equal effe
cts or normally distributed effects. (C) Inra/Elsevier, Paris.