Inomata Nobuyuki, Goto Hiroki, Itoh Masanobu, Isono Kunio
Department of Biology, Graduate School of Sciences, Kyushu University, Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan.
Genetics. 2004 Aug;167(4):1749-58. doi: 10.1534/genetics.104.027045.
Variation in trehalose sensitivity and nucleotide sequence polymorphism of the Gr5a gene encoding the gustatory receptor to sugar trehalose were investigated in 152 male lines of Drosophila melanogaster collected from a natural population. Among the observed 59 segregating sites, some pairs of sites showed significant linkage disequilibrium. A single SNP, which results in the Ala218Thr amino acid change, was significantly associated with trehalose sensitivity, as previously suggested. Threonine at amino acid position 218 was found to be the ancestral form in D. melanogaster, suggesting that low trehalose sensitivity was an ancestral form with respect to the receptor function. There was large genetic variation in trehalose sensitivity. It was continuously distributed, indicating that trehalose sensitivity measured by the behavioral assay is a quantitative trait. These results suggest that apart from the Gr5a gene, other genetic factors contribute to variation in trehalose sensitivity. Nucleotide diversity (pi) and nucleotide variation (theta) per site were 0.00874 and 0.00590, respectively. Fu and Li's test and the MK test showed no significant departure from the expectation of selective neutrality in the Gr5a gene. However, we rejected selective neutrality by Tajima's test and Fay and Wu's test with the observed level of recombination. We discuss possible causes of the observed pattern of nucleotide variation in the gustatory receptor Gr5a gene.
在从自然种群中收集的152个黑腹果蝇雄性品系中,研究了编码对海藻糖味觉受体的Gr5a基因的海藻糖敏感性变异和核苷酸序列多态性。在观察到的59个分离位点中,一些位点对显示出显著的连锁不平衡。如先前所示,一个导致Ala218Thr氨基酸变化的单核苷酸多态性(SNP)与海藻糖敏感性显著相关。发现第218位氨基酸的苏氨酸是黑腹果蝇的祖先形式,这表明就受体功能而言,低海藻糖敏感性是祖先形式。海藻糖敏感性存在很大的遗传变异。它呈连续分布,表明通过行为测定法测量的海藻糖敏感性是一个数量性状。这些结果表明,除了Gr5a基因外,其他遗传因素也导致海藻糖敏感性的变异。每个位点的核苷酸多样性(pi)和核苷酸变异(theta)分别为0.00874和0.00590。Fu和Li检验以及MK检验表明,Gr5a基因没有明显偏离选择性中性的预期。然而,通过Tajima检验和Fay和Wu检验以及观察到的重组水平,我们拒绝了选择性中性。我们讨论了味觉受体Gr5a基因中观察到的核苷酸变异模式的可能原因。