Immunohistochemistry of Active Gibberellins and Gibberellin-Inducible α-Amylase in Developing Seeds of Morning Glory

Author:

Nakayama Akira1,Park Seijin1,Zheng-Jun Xu12,Nakajima Masatoshi1,Yamaguchi Isomaro1

Affiliation:

1. Department of Applied Biological Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo 113–8657, Japan (A.N., S.P., X.Z.-J., M.N., I.Y.); and

2. Bio-oriented Technology Research Advancement Institution (BRAIN), Minato-ku, Tokyo 105–0001, Japan (X.Z.-J.)

Abstract

Abstract Gibberellins (GAs) in developing seeds of morning glory (Pharbitis nil) were quantified and localized by immunostaining. The starch grains began to be digested after the GA contents had increased and reached a plateau. Immunohistochemical staining with the antigibberellin A1-methyl ester-antiserum, which has high affinity to biologically active GAs, showed that GA1 and/or GA3 were localized around starch grains in the integument of developing young seeds, suggesting the participation of GA-inducible α-amylase in this digestion. We isolated an α-amylase cDNA (PnAmy1) that was expressed in the immature seeds, and using an antibody raised against recombinant protein, it was shown that PnAmy1 was expressed in the immature seeds. GA responsiveness of PnAmy1 was shown by treating the young fruits 9 d after anthesis with GA3. RNA-blot and immunoblot analyses showed that PnAmy1 emerged soon after the rapid increase of GA1/3. An immunohistochemical analysis of PnAmy1 showed that it, like the seed GA1/3, was also localized around starch grains in the integument of developing young seeds. The localization of GA1/3 in the integument coincident with the expression of PnAmy1 suggests that both function as part of a process to release sugars for translocation or for the further development of the seeds.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

Reference28 articles.

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