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   <subfield code="a">Molecular Cloning and Nucleotide Sequences of cDNAs Encoding S-Allele Specific Stylar RNases in a Self-Incompatible Cultivar and Its Self-compatible Mutant of Japanese Pear, Pyrus pyrifolia Nakail</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Naoko Norioka, Shigemi Norioka, Yoshimi Ohnishi, Takeshi Ishimizu, Chitose Oneyama, Tetsu Nakanishi, Fumio Sakiyama]</subfield>
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   <subfield code="a">The genes encoding three RNases were cloned from the style of a self-incompatible cultivar, Nijisseiki (S2S4), and its self-compatible mutant, Osa-Nijisseiki (S2S4sm, sm means stylar part mutant), of Japanese pear. For Nijisseiki, cDNAs coding for two S-RNases (S2-RNase and S4-RNase) and an RNase unrelated to self-incompatibility (non-S-RNase) were cloned from the stylar cDNA library. The cDNAs coding for S2-RNase, S4-RNase, and non-S-RNase include 678-, 684, and 681-bp open reading frames, respectively. Their deduced amino acid sequences were composed of signal peptides and mature RNases (201-203 residues) which were verified by partial amino acid sequencing. The primary structures of mature proteins revealed that these RNasea are of the RNase T2 type; only the two S-RNases have several potential N-glycosylation sites and 60% of their amino acid residues are identical, compared with 25% sequence identity with the non-S-RNase. Such a distinct difference in the primary structures between S-RNases and non-S-RNase has not previously been reported and may be a feature typical of S-RNases in the family Rosaceae. Similar experiments were performed for Osa-Nijisseiki. The cDNAs coding for S2-RNaae and non-S4-RNase were similarly cloned from the stylar cDNA library. However, the cDNA coding for S4-RNase was neither amplified by PCR nor cloned from the library, suggesting that the mutation of self-incompatible Nijisseiki to self-compatible Osa-Nijisseiki is due to a failure of expression of S4-RNase. These results lead to the idea that Osa-Nijisseiki is a variant of Nijisseiki in which the S4-allelic gene in the S-locus is exclusively mutated or deleted, causing severely impaired or suppressed expression of its gene product, S4-RNase,at the style.</subfield>
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   <subfield code="a">© 1996 BY THE JOURNAL OF BIOCHEMISTRY</subfield>
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   <subfield code="a">Norioka</subfield>
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   <subfield code="u">Division of Protein Chemistry, Institute for Protein Research, Osaka University Suita, Osaka 565</subfield>
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