Nucleic Acids Research, Vol 24, Issue 23 4798-4804, Copyright © 1996 by Oxford University Press
C Lelandais, S Gutierres, C Mathieu, F Vedel, C Remacle, L Marechal-Drouard, A Brennicke, S Binder and P Chetrit
The expression of two mitochondrial gene clusters (orf87-nad3-nad1/A and
orf87-nad3-rps12) was studied in Nicotiana sylvestris. 5' and 3' termini of
transcripts were mapped by primer extension and nuclease S1 protection.
Processing and transcription initiation sites were differentiated by in
vitro phosphorylation and capping experiments. A transcription initiation
site, present in both gene clusters, was found 213 nucleotides upstream of
orf87. This promoter element matches the consensus motif for dicotyledonous
mitochondrial promoters and initiates run-off transcription in a pea
mitochondrial purified protein fraction. Processing sites were identified
5' of nad3, nad1/A and rps12 respectively. These results suggest that (i)
the expression of the two cistrons is only controlled by one duplicated
promoter element, and (ii) multiple processing events are required to
produce monocistronic nad3, nad1/A and rps12 transcripts.
ARTICLES
A promoter element active in run-off transcription controls the expression of two cistrons of nad and rps genes in Nicotiana sylvestris mitochondria
Institut de Biotechnologie des Plantes, URA 1128, Universite Paris-Sud, Orsay, France.
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