Iron-regulated ferritin synthesis in animals is dominated by translational control of stored mRNA; ironinduced transcription of ferritin genes, when it occurs, changes the subunit composition of ferritin mRNA and protein and is coupled to translational control. Ferritins in plants and animals have evolved from a common progenitor, based on the simi-
Spinach cell suspension cultures maintained in photomixotrophic conditions exhibit plastids which undergo cyclic morphological transformations along a growth cycle. Ultrastructural studies show that the green chloroplasts present at the initial stage differentiate into amyloplasts during the subsequent log phase and then return to chloroplasts in stationary phase. The changes of the levels of plastid DNA (pt DNA) per cell have been determined along the growth cycle, as a percentage of total DNA by hybridization of definite amounts of total DNA to a radioactive probe of cloned pt DNA. The number of pt DNA copies have been estimated to 1125 per cell at the maximum of amyloplast development and to 5940 copies per cell at the maximum of chloroplast differentiation. Hybridizations of defined amounts of total cellular RNA to labelled probes of the 16S rDNA and of the rbcL gene allowed estimations of the variations of the corresponding cellular RNA pools. These variations are well correlated with the changes of the ptDNA cellular levels. These results show that the ptDNA gene dosage plays a central role in the regulation of the plastid transcript levels in this system.
Two potential prokaryotic promoters, P1 and P2, are characterized 164 and 114 bp upstream of the spinach chloroplast 16S rRNA gene. The strengths of these promoters, calculated according to an homology score established for E. coli RNA-polymerase, are identical. Experiments performed with a Taq I-DNA fragment, containing 16 bp of the 16S rDNA and 243 bp upstream of the gene, give evidence that in vitro, E. coli RNA-polymerase starts transcription at these two promoters. These results are based on both the size of the transcripts and their nucleotide sequences. A possible regulation by differential control of these dual promoters is suggested. S1 mapping with RNAs extracted either from green or from etiolated spinach plants, indicates that, at these two steps of plastid development, transcription in vivo starts at P1. Surprisingly only P2 appears to be conserved in the homologous sequences reported for maize, mustard and Spirodela.
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