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. 1986 Jan;83(2):361–365. doi: 10.1073/pnas.83.2.361

Specific heat shock proteins are transported into chloroplasts

Elizabeth Vierling 1,*, Michael L Mishkind 1,†, Gregory W Schmidt 1, Joe L Key 1
PMCID: PMC322858  PMID: 16593647

Abstract

We demonstrate that in three plant species—soybean, pea, and corn—certain nuclear-encoded heat shock proteins are transported into chloroplasts. In vitro translation products of poly(A)-RNA from control or heat-shocked plants were incubated with isolated intact pea chloroplasts and differences in the profile of imported proteins were analyzed. In all three species, abundant polypeptides between 21 and 27 kDa are present in the heat shock sample and absent in the controls. These polypeptides are protected from trypsin and chymotrypsin digestion after their import into chloroplasts and are recovered primarily with the soluble chloroplast protein fraction. Chloroplasts isolated from pea or corn leaves labeled in vivo at heat shock temperatures, but not at normal growth temperatures, contain the same polypeptides observed in vitro. Synthesis of the heat shock polypeptides can be inhibited in vivo by cycloheximide but not by chloramphenicol, further indicating they are products of cytoplasmic protein synthesis. The in vitro transport experiments demonstrate that synthesis of the chloroplast-localized heat shock proteins results from heat-induced accumulation of the corresponding poly(A)-RNAs. The same mRNAs are also produced in response to heat shock by a nonphotosynthetic tissue, the etiolated soybean hypocotyl.

Keywords: in vitro protein transport, stress proteins, heat shock mRNA, organelle protein synthesis

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