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PLANT PHYSIOLOGY , Vol 101, Issue 2 451-458, Copyright © 1993 by American Society of Plant Biologists
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CELL BIOLOGY AND SIGNAL TRANSDUCTION |
Colocalization of Barley Lectin and Sporamin in Vacuoles of Transgenic Tobacco Plants
M. R. Schroeder, O. N. Borkhsenious, K. Matsuoka, K. Nakamura and N. V. Raikhel
Department of Energy Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824-1312 (M.R.S., O.N.B., N.V.R.)
Various targeting motifs have been identified for plant proteins delivered
to the vacuole. For barley (Hordeum vulgare) lectin, a typical Gramineae
lectin and defense-related protein, the vacuolar information is contained
in a carboxyl-terminal propeptide. In contrast, the vacuolar targeting
information of sporamin, a storage protein from the tuberous roots of the
sweet potato (Ipomoea batatas), is encoded in an amino-terminal propeptide.
Both proteins were expressed simultaneously in transgenic tobacco plants to
enable analysis of their posttranslational processing and subcellular
localization by pulse-chase labeling and electron-microscopic
immunocytochemical methods. The pulse-chase experiments demonstrated that
processing and delivery to the vacuole are not impaired by the simultaneous
expression of barley lectin and sporamin Both proteins were targeted
quantitatively to the vacuole, indicating that the carboxyl-terminal and
amino-terminal propeptides are equally recognized by the vacuolar
protein-sorting machinery. Double-labeling experiments showed that barley
lectin and sporamin accumulate in the same vacuole of transgenic tobacco
(Nicotiana tabacum) leaf and root cells.
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