1989
DOI: 10.1128/mcb.9.12.5650-5659.1989
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In Vitro Analysis of the Pea Chloroplast 16S rRNA Gene Promoter

Abstract: A cloned pea chloroplast 16S rRNA gene promoter has been characterized in detail by use of a homologous in vitro transcription system that contains a highly purified chloroplast RNA polymerase. The in vivo and in vitro 16S rRNA transcriptional start site has been identified to be a T on the plus strand, 158 bases upstream of the mature 5' end of the gene. BAL 31 deletions of the 16S rRNA leader region demonstrated that the bases between -66 to +30 relative to the transcriptional start site (+1) are necessary f… Show more

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(4 citation statements)
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“…Interestingly, clpP is transcribed from the PclpP –53 NEP promoter in wild‐type leaves while most other NEP promoters are inactive in the same tissue. Differential accumulation of mRNAs from NEP promoters is possibly due to regulation by nuclear‐encoded factors via gene‐specific promoter elements, as reported for σ 70 ‐type PEP promoters (Sun et al ., 1989; Iratni et al ., 1994; Allison and Maliga, 1995; Kim and Mullet, 1995).…”
Section: Discussionmentioning
confidence: 55%
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“…Interestingly, clpP is transcribed from the PclpP –53 NEP promoter in wild‐type leaves while most other NEP promoters are inactive in the same tissue. Differential accumulation of mRNAs from NEP promoters is possibly due to regulation by nuclear‐encoded factors via gene‐specific promoter elements, as reported for σ 70 ‐type PEP promoters (Sun et al ., 1989; Iratni et al ., 1994; Allison and Maliga, 1995; Kim and Mullet, 1995).…”
Section: Discussionmentioning
confidence: 55%
“…Group II includes plastid genes encoding mRNAs that factors interacting with elements upstream of the core promoter (Sun et al, 1989;Iratni et al, 1994; Allison accumulate to significant levels in both wild-type and ΔrpoB leaves (Figure 1B). Group II includes atpB (ATP and Maliga, 1995;Kim and Mullet, 1995).…”
Section: Introduction Resultsmentioning
confidence: 99%
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