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PLANT PHYSIOLOGY , Vol 106, Issue 4 1659-1665, Copyright © 1994 by American Society of Plant Biologists
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MOLECULAR BIOLOGY AND GENE REGULATION |
Structural Features of the Maize sus1 Gene and Protein
J. R. Shaw, R. J. Ferl, J. Baier, D. St Clair, C. Carson, D. R. McCarty and L. C. Hannah
Program in Plant Molecular and Cellular Biology and Department of Horticultural Sciences, University of Florida, Gainesville, Florida 32611
Genomic clones, cDNA clones, and protein of the maize (Zea mays L.) Suc
synthase1 (sus1) gene were isolated and sequenced. Termini (5[prime] and
3[prime]) of the transcribed unit were identified. The SUS1 protein was
purified 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 sus1 This
intron bears much sequence similarity with the adjacent exon, suggesting
that the intron arose from an internal duplication. Although 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 differential rate of divergence of exons
and introns is selection pressure for gene function. Additionally,
comparisons of coding regions of plant sucrose synthases show that sh1-like
and sus1-like genes can be found in all monocots so far analyzed. These
latter observations point to an important role played by both genes in this
group of plants.
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