Chung I K, Ito T, Tanaka H, Ohta A, Nan H G, Takagi M
Department of Agricultural Chemistry, University of Tokyo, Japan.
Plant Mol Biol. 1994 Oct;26(2):757-62. doi: 10.1007/BF00013760.
We isolated S allele-associated cDNA clones from each of the stylar cDNA libraries of Lycopersicon peruvianum of two different S genotypes (S12Sb and S13Sc) with S11Sa allele-associated cDNA (LPS11) as a probe. The longest cDNA clones, designated LPS12 and LPS13, which were 779 bp and 853 bp in length, contained open reading frames of 189 and 210 amino acids, respectively. The three S allele-associated cDNAs (LPS11, LPS12, and LPS13) did not cross-hybridize to each other under highly stringent condition by northern blot analysis. Their average identity to Nicotiana alata S-proteins so far was 49%. The fragments corresponding to LPS11 or LPS12 cosegregated with their respective S alleles in genetic crosses. From these results, we conclude that the three cloned cDNAs were derived from the three different S alleles of L. peruvianum.
我们以S11Sa等位基因相关的cDNA(LPS11)为探针,从两种不同S基因型(S12Sb和S13Sc)的秘鲁番茄花柱cDNA文库中分离出S等位基因相关的cDNA克隆。最长的cDNA克隆,分别命名为LPS12和LPS13,长度分别为779 bp和853 bp,分别包含189和210个氨基酸的开放阅读框。通过Northern印迹分析,在高度严格的条件下,这三个S等位基因相关的cDNA(LPS11、LPS12和LPS13)彼此不发生交叉杂交。到目前为止,它们与烟草S蛋白的平均同一性为49%。在遗传杂交中,与LPS11或LPS12对应的片段与其各自的S等位基因共分离。从这些结果中,我们得出结论,这三个克隆的cDNA来自秘鲁番茄的三个不同S等位基因。