ABSTRACIWhen isolated pea plastids are incubated with translation products of poly(A') mRNA they specifically import precursor molecules of plastid polypeptides. Etioplasts and chloroplasts import the same polypeptides from identical translation products, and, the imported polypeptides can be well resolved by two-dimensional gel electrophoresis. Therefore, the posttranslational uptake system using isolated chloroplasts can monitor changes in the abundance of translatable plastid-targeted messages. Poly(A') mRNA was isolated from peas at various times during greenig and analyzed by this technique. (a) After 48 hours of illumination of dark-gown plants, the relative portion of npelear eitcoded messages for plastid targeted proteins had increased by a factor of 2. The percentage of polypeptides recovered in the stroma fraction increased from about 50 to 65%. (b) More than 140 imported polypeptide species could be detected in fluorograms of two-dimensional gels, most of which could be identified throughout the time course ofgreening. At least 37 imported polypeptides decreased and 36, increased in relative abundance during greening of darkgreen plants. (c) In most cases, where differences In translatable messages were seen between dark-and light-grown plants, they were accompanied by parallel changes in polypeptide abundance.Most plastid polypeptides are encoded by nuclear genes. However, experimental data regarding the regulation of polypeptide and transcript abundance during greening is limited to a few polypeptides. Our understanding of the regulation of the two most prominent nuclear encoded chloroplast polypeptides, the SSU3 and LHCP, has increased during the last years due to the work of several research groups. As with all nuclear encoded plastid proteins whose amino acid sequences have been described, SSU and LHCP are synthesized as precursor molecules on cytoplasmic ribosomnes and their primary translation products possess aminoterminal extensions (7) In this line of consecutive events, well established for these two polypeptides, several different points of regulatory control can be easily imagined: regulation at the level of transcription; RNA stability; regulation of translation; precursor stability in the cytosol; rate and specificity ofuptake; processing ofthe imported precursors; assembly in the presence ofthe corresponding factors; and rate of degradation inside the plastid (5,12,22).In