
doi: 10.1007/bf00013760
pmid: 7948929
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.
Nicotiana, DNA, Complementary, Base Sequence, Sequence Homology, Amino Acid, Molecular Sequence Data, Genetic Variation, Plants, Genes, Plant, Polymerase Chain Reaction, Open Reading Frames, Plants, Toxic, Amino Acid Sequence, Alleles, DNA Primers, Gene Library, Glycoproteins, Plant Proteins
Nicotiana, DNA, Complementary, Base Sequence, Sequence Homology, Amino Acid, Molecular Sequence Data, Genetic Variation, Plants, Genes, Plant, Polymerase Chain Reaction, Open Reading Frames, Plants, Toxic, Amino Acid Sequence, Alleles, DNA Primers, Gene Library, Glycoproteins, Plant Proteins
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