Identification of a growth phase-dependent promoter in the rplJL operon ofStreptomyces coelicolor A3(2)

Citation
G. Blanco et al., Identification of a growth phase-dependent promoter in the rplJL operon ofStreptomyces coelicolor A3(2), BBA-GENE ST, 1517(2), 2001, pp. 243-249
Citations number
43
Categorie Soggetti
Molecular Biology & Genetics
Journal title
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
ISSN journal
01674781 → ACNP
Volume
1517
Issue
2
Year of publication
2001
Pages
243 - 249
Database
ISI
SICI code
0167-4781(20010126)1517:2<243:IOAGPP>2.0.ZU;2-B
Abstract
A single promoter, rplJp (P-L10), has been identified in the rplJL operon f rom Streptomyces coelicolor A3(2) by promoter probe and primer extension an alyses. P-L10 is located upstream of the rplL gene and of the DNA encoding the mRNA leader region that contains the putative L10 (or L10.L12(4)) bindi ng site for translational autogenous regulation. The potential start point for transcription was found 239 nucleotides upstream of the predicted trans lational start codon of rplJ. The promoter sequence shows -35 and -10 hexam ers that resemble those of Streptomyces consensus Escherichia coli sigma (7 0)-like promoters and the rplJp From Streptomyces griseus. The amount of th e transcript detected by primer extension analysis decreases during growth immediately after the transition phase, a slowdown in growth occurring duri ng exponential phase associated with increases in ppGpp level. The temporal pattern of transcripts shows a clear correlation with the temporal pattern of L10 and L7/L12 protein synthesis reported in previous kinetic studies. This indicates that PL10 is a growth phase-dependent promoter which may con tribute, together with translational regulation, to the decrease in the syn thesis of L10 and L7/L12 observed in liquid minimal medium. This is support ed by results of promoter probe experiments. Although no significant promot er activity has been found by promoter probing in the rplJ and rplL interge nic region, an additional 5'-transcript end was detected by primer extensio n, probably as a result of mRNA processing event from a longer transcript. This may be required to maintain the 1:4 ratio observed for L10 and L7/L12 in the ribosomes. (C) 2001 Elsevier Science B.V. All rights reserved.