Author:
Mella R. A.,Sànchez R. A.,Maldonado S.
Abstract
In Datura ferox L. seeds induced to germinate by the far-red light absorbing form of phytochrome (Pfr) and alternating temperatures, protein degradation started before radicle protrusion. Proteolysis was, however, restricted to the micropylar region of the endosperm in which the protein content decreased 51% by 48 h after red light treatment. There was no change during that time in the protein content of the rest of the endosperm or in the embryo. Light and electron microscopy preparations show the vacuolation of protein bodies along with other changes in cellular structure in the micropylar portion of the endosperm in seeds treated with red light (R). No changes were detected in the rest of the endosperm or in the micropylar portions of far-red light (FR) treated seeds. In the embryonic axes there were some alterations but only in a small sector of the calyptra. In contrast, shortly after radicle protrusion (5 h), there was extensive degradation of protein bodies in the embryonic axes. A Pfr is required for the induction of protein degradation in the micropylar portion of the endosperm in the intact seed before radicle protrusion. Incubation of isolated micropylar portions induced protein degradation in tissues from seeds treated with either R or FR. The results do not support a source–sink type of control of protein degradation in the endosperm driven by the beginning of embryo growth but suggest the participation of regulatory signals in the determination of a temporal and spatial pattern of protein degradation in both the endosperm and the embryo. Key words: germination, dormancy, phytochrome, protein degradation, micropylar endosperm.
Publisher
Canadian Science Publishing
Cited by
23 articles.
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