Genomic clones, cDNA clones, and protein of the maize (Zea mays L.) Su
c synthase1 (sus1) gene were isolated and sequenced. Termini (5' and 3
') of the transcribed unit were identified. The SUS1 protein was purif
ied from tissue culture cells as a phosphorylated protein. The overall
structure of sus1 is virtually identical with that of the paralogous
gene, shrunken1 (sh1); however, the last intron of sh1 is missing in s
us1. This intron bears much sequence similarity with the adjacent exon
, suggesting that the intron arose from an internal duplication. Altho
ugh the placement of the other 14 introns is identical in both genes,
the introns exhibit markedly greater differences in size and sequence
relative to that shown by the exons. An explanation for the differenti
al rate of divergence of exons and introns is selection pressure for g
ene function. Additionally, comparisons of coding regions of plant suc
rose synthases show that sh1-like and sus1-like genes can be found in
all monocots so far analyzed. These latter observations point to an im
portant role played by both genes in this group of plants.