| Literature DB >> 28011633 |
Nader Aryamanesh1,2, Hannes Ruwe1,2, Lilian Vincis Pereira Sanglard1,2, Leila Eshraghi1,2, John D Bussell1,2, Katharine A Howell1,2, Ian Small3,4, Catherine Colas des Francs-Small3,4.
Abstract
We report the partial complementation and subsequent comparative molecular analysis of two nonviable mutants impaired in chloroplast translation, one (emb2394) lacking the RPL6 protein, and the other (emb2654) carrying a mutation in a gene encoding a P-class pentatricopeptide repeat protein. We show that EMB2654 is required for the trans-splicing of the plastid rps12 transcript and that therefore the emb2654 mutant lacks Rps12 protein and fails to assemble the small subunit of the plastid ribosome, explaining the loss of plastid translation and consequent embryo-lethal phenotype. Predictions of the EMB2654 binding site match a small RNA "footprint" located on the 5' half of the trans-spliced intron that is almost absent in the partially complemented mutant. EMB2654 binds sequence specifically to this target sequence in vitro. Altered patterns in nuclease-protected small RNA fragments in emb2654 show that EMB2654 binding must be an early step in, or prior to, the formation of a large protein-RNA complex covering the free ends of the two rps12 intron halves.Entities:
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Year: 2016 PMID: 28011633 PMCID: PMC5291019 DOI: 10.1104/pp.16.01840
Source DB: PubMed Journal: Plant Physiol ISSN: 0032-0889 Impact factor: 8.340