We sought to determine the genetic basis of expression of the ubiquito
us (metabolic) urease of soybean. This isozyme is termed the metabolic
urease because its loss, in eu4/eu4 mutants, leads to accumulation of
urea, whereas loss df the embryo-specific urease isozyme does not. Th
e eu4 lesion eliminated the expression of the ubiquitous urease in veg
etative and embryonic tissues. RFLP analysis placed urease clone LC4 n
ear, or within, the Eu4 locus. Sequence comparison of urease proteins
(ubiquitous and embryo-specific) and clones (LC4 and LS1) indicated th
at LC4 and LS1 encode ubiquitous and embryo-specific ureases, respecti
vely. That LC4 is transcribed into poly(A)(+) RNA in all tissues was i
ndicated by the amplification of its transcript by an LC4-specific PCR
primer. (The LS1-specific primer, on the other hand, amplified poly(A
)(+) RNA only from developing embryos expressing the embryo-specific u
rease.) These observations are consistent with Eu4 being the ubiquitou
s urease structural gene contained in the LC4 clone. In agreement with
this notion, the mutant phenotype of eu4/eu4 callus was partially cor
rected by the LC4 urease gene introduced by particle bombardment.