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首页> 外文期刊>Nucleic acids research >An additional promoter within the protein-coding region of the psbD-psbC gene cluster in tobacco chloroplast DNA
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An additional promoter within the protein-coding region of the psbD-psbC gene cluster in tobacco chloroplast DNA

机译:烟草叶绿体DNA中psbD-psbC基因簇的蛋白质编码区内的另一个启动子

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Transcription of the psbD-psbC gene cluster in tobacco chloroplasts has been studied. This cluster contains in linear sequence the overlapping genes encoding the D2 and 43 kDa proteins of Photosystem II (psbD and psbC, respectively), and 0RF62. Eight major transcripts ranging from 1.5 to 4.4 kb were detected by northern blot analysis. S1 mapping experiments revealed that these multiple transcripts comprise five distinct 5′ ends whose precise positions were further determined by primer extension analysis. Two of the five 5′ ends were determined to be the transcriptional initiation sites by in vitro capping assays: the main site is located 905 bp upstream from the ATG codon of psbD and the additional site is 194 bp upstream from the first ATG codon of psbC. The latter site and the preceding prokaryotic promoter motif are within the protein-coding region of psbD. The 3′ ends of transcripts were determined by S1 mapping.
机译:研究了烟草叶绿体中psbD-psbC基因簇的转录。该簇包含线性序列的重叠基因,这些基因编码光系统II的D2和43 kDa蛋白(分别为psbD和psbC)和0RF62。通过RNA印迹分析检测到1.5至4.4kb范围内的八个主要转录物。 S1作图实验表明,这些多个转录物包含五个不同的5'末端,其精确位置通过引物延伸分析进一步确定。 5个5'末端中的2个已通过体外加盖分析确定为转录起始位点:主要位点位于psbD的ATG密码子上游905 bp,另一个位点位于psbC的第一个ATG密码子上游194 bp。 。后面的位点和前面的原核启动子基序在psbD的蛋白质编码区内。转录物的3'端通过S1作图确定。

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