Expression of two uricase (Nodulin-35) genes in a non-ureide type legume, Medicago sativa

Two cDNA clones, MsU2 and MsU9 encoding uricase (EC 1.7.3.3, Nodulin-35) we re isolated from a cDNA library prepared from nodule tissues of alfalfa, Me dicago sativa, plants. Both MsU2 and MsU9 encoded 308 amino acid polypeptid es with a difference of 5 amino acids, and the deduced amino acid sequences shared 98% homology. Between these two cDNA clones and uricase genes of so ybean which were designated as Nod-35s, more than 80% identity was observed in nucleotides and deduced amino acid sequences, suggesting that these MsU 2 and MsU9 are homologs of Nod-35. Using the reverse transcription-PCR technique, we detected the transcripts of these two genes in almost all tissues of alfalfa. The operation of urica se genes was confirmed by the presence of ureide in the xylem sap and urica se activity in the nodules. In situ hybridization analysis revealed that Ms U2 and MsU9 were expressed only in uninfected cells of the infected zone of the nodule tissue. The cell specific-expression of the two uricase genes w as observed in an identical manner to that of Nod-35 in soybean nodules.