Kato S, Mukai Y
Department of Forest Resources Science, Faculty of Agriculture, University of Shizuoka, Shizuoka 422-8529, Japan.
Heredity (Edinb). 2004 Mar;92(3):249-56. doi: 10.1038/sj.hdy.6800403.
In the Rosaceae family, which includes Prunus, gametophytic self-incompatibility (GSI) is controlled by a single multiallelic locus (S-locus), and the S-locus product expressed in the pistils is a glycoprotein with ribonuclease activity (S-RNase). Two populations of flowering cherry (Prunus lannesiana var. speciosa), located on Hachijo Island in Japan's Izu Islands, were sampled, and S-allele diversity was surveyed based on the sequence polymorphism of S-RNase. A total of seven S-alleles were cloned and sequenced. The S-RNases of flowering cherry showed high homology to those of Prunus cultivars (P. avium and P. dulcis). In the phylogenetic tree, the S-RNases of flowering cherry and other Prunus cultivars formed a distinct group, but they did not form species-specific subgroups. The nucleotide substitution pattern in S-RNases of flowering cherry showed no excess of nonsynonymous substitutions relative to synonymous substitutions. However, the S-RNases of flowering cherry had a higher Ka/Ks ratio than those of other Prunus cultivars, and a subtle heterogeneity in the nucleotide substitution rates was observed among the Prunus species. The S-genotype of each individual was determined by Southern blotting of restriction enzyme-digested genomic DNA, using cDNA for S-RNase as a probe. A total of 22 S-alleles were identified. All individuals examined were heterozygous, as expected under GSI. The allele frequencies were, contrary to the expectation under GSI, significantly unequal. The two populations studied showed a high degree of overlap, with 18 shared alleles. However, the allele frequencies differed considerably between the two populations.
在包括李属在内的蔷薇科中,配子体自交不亲和性(GSI)由单个复等位基因位点(S位点)控制,雌蕊中表达的S位点产物是一种具有核糖核酸酶活性的糖蛋白(S-RNase)。对位于日本伊豆诸岛八丈岛上的两个樱花(Prunus lannesiana var. speciosa)种群进行了采样,并基于S-RNase的序列多态性对S等位基因多样性进行了调查。共克隆并测序了7个S等位基因。樱花的S-RNase与李属栽培品种(欧洲甜樱桃和甜扁桃)的S-RNase具有高度同源性。在系统发育树中,樱花和其他李属栽培品种的S-RNase形成了一个独特的群体,但它们没有形成物种特异性的亚群。樱花S-RNase中的核苷酸替换模式显示,非同义替换相对于同义替换没有过量。然而,樱花的S-RNase的Ka/Ks比值高于其他李属栽培品种,并且在李属物种之间观察到核苷酸替换率存在细微的异质性。使用S-RNase的cDNA作为探针,通过对限制性内切酶消化的基因组DNA进行Southern印迹分析,确定了每个个体的S基因型。共鉴定出22个S等位基因。所有检测的个体都是杂合子,这与GSI预期一致。与GSI预期相反,等位基因频率显著不等。所研究的两个种群显示出高度的重叠,有18个共享等位基因。然而,两个种群之间的等位基因频率差异很大。