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Mol. Cell. Biol., Jun 1997, 3440-3448, Vol 17, No. 6
W Zerges, J Girard-Bascou and JD Rochaix
Translation of the chloroplast psbC mRNA in Chlamydomonas reinhardtii has
been shown previously to require interactions between its 5' untranslated
region (5' UTR) and the functions encoded by two nuclear loci, which we
name here TBC1 and TBC2. We show that a 97-nucleotide (nt) region located
in the middle of the psbC 5' UTR is required for translation initiation.
Unlike most procaryotic cis-acting translational control elements, this
region has a translational activation function and is located 236 nt
upstream from the GUG translation initiation codon. In vivo pulse-labeling
of chloroplast- encoded proteins and analyses of the expression of chimeric
reporter genes in vivo reveal that a mutation of a newly described locus,
TBC3, restores translation from the psbC 5' UTR in the absence of either
this cis-acting element or the wild-type trans-acting TBC1 function. These
data demonstrate that sequences located in the middle of the psbC 5' UTR,
TBC1, and TBC3 functionally interact to control the translation of the psbC
mRNA.
Copyright © 1997, American Society for Microbiology
Translation of the chloroplast psbC mRNA is controlled by interactions between its 5' leader and the nuclear loci TBC1 and TBC3 in Chlamydomonas reinhardtii
Department of Molecular Biology, University of Geneva, Switzerland. William.Zerges@molbio.unige.ch
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