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Plant Physiol, February 2001, Vol. 125, pp. 1012-1022

Evidence That Intragenic Recombination Contributes to Allelic Diversity of the S-RNase Gene at the Self-Incompatibility (S) Locus in Petunia inflata1

Xi Wang, Austin L. Hughes, Tatsuya Tsukamoto, Toshio Ando, and Teh-Hui Kao*

Department of Biochemistry and Molecular Biology (X.W., T.-H.K.) and Intercollege Graduate Degree Program in Plant Physiology (T.-H.K.), Pennsylvania State University, University Park, Pennsylvania 16802; Department of Biological Sciences, University of South Carolina, Columbia, South Carolina 29208 (A.L.H.); and Faculty of Horticulture, Chiba University, 648 Matsudo, Chiba 271-8510, Japan (T.T., T.A.)

For Solanaceae type self-incompatibility, discrimination between self and nonself pollen by the pistil is controlled by the highly polymorphic S-RNase gene. To date, the mechanism generating the allelic diversity of this gene is largely unknown. Natural populations offer a good opportunity to address this question because they likely contain different alleles that share recent common progenitors. We identified 19 S haplotypes from a natural population of Petunia inflata in Argentina, used reverse transcriptase-polymerase chain reaction to obtain cDNAs for 15 alleles of the S-RNase gene, and sequenced all the cDNAs. Phylogenetic studies revealed that five of these alleles and two previously identified alleles form a major clade, and that the 5' region of S19 allele was derived from an ancestor allele closely related to S2, whereas its 3' region was derived from an ancestor allele closely related to S8. A similar evolutionary relationship was found among S3, S12, and S15 alleles. These findings suggest that intragenic recombination contributed to the generation of the allelic diversity of the S-RNase gene. Two additional findings emerged from the sequence comparisons. First, the nucleotide sequence of the S1 allele identified in this work is completely identical to that of the previously identified S1 allele of a different origin. Second, in the two hypervariable regions HVa and HVb, thought to be involved in determining S allele specificity, S6 and S9 alleles differ only by four nucleotides, all in HVb, resulting in two amino acid differences. The implications of these findings are discussed.


1 This work was supported by the National Science Foundation (grant nos. IBN-9603993 and IBN-9982659 to T.-H.K.) and by the National Institutes of Health (grant no. GM34940 to A.L.H.).

* Corresponding author; e-mail: txk3{at}psu.edu; fax 814-863- 9416.

© 2001 American Society of Plant Physiologists



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