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Photoaffinity labelling of the pea chloroplast transcriptional complex by nascent RNA in vitro.

机译:体外初生RNA对豌豆叶绿体转录复合物的光亲和性标记。

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摘要

We have used photoaffinity labelling to examine the chloroplast RNA polymerase components which come into contact with nascent transcripts during the in vitro transcription of plastid DNA. The transcripts were synthesized in the presence of a photoactive analogue (4-thio UTP) and alpha-32P-ATP, using enriched pea chloroplast RNA polymerase preparation and a recombinant plasmid containing the plastid 16S rRNA promoter. Brief irradiation of the transcriptional complex crosslinked the photoactive nascent RNA to proximal proteins. Labelling of the transcriptional complex was dependent on 4-thio UTP and template DNA. Two polypeptides of 51 and 54 kDa were consistently crosslinked to the nascent transcripts; about 60% of the total radioactivity of the crosslinked RNA was associated with these polypeptides. In some experiments, two additional polypeptides of 38 and 75 kDa were also found to be associated with about 13% and 17% of the total crosslinked RNA radioactivity, respectively. The UV-crosslinked transcriptional complexes were stable to either DNase or S1 nuclease hydrolysis but partially sensitive to RNase T1. Insensitivity of the complex to hydrolysis with RNase H suggested that the nascent transcripts were not crosslinked to the template. The complexes could also be hydrolysed by proteinase K and thermolysin. No crosslinkage was observed when labelled RNA molecules containing 4-thio UMP residues were added after synthesis to the polymerase preparation. This suggested that the method identified only those polypeptides which came into close contact with the transcript during its synthesis. Antibodies raised against the RNA-protein complex confirmed the presence of the polypeptides in the chloroplast RNA polymerase preparation on Western blots. Preincubation of these antibodies with the chloroplast RNA polymerase inhibited plastid DNA transcription. These data showed that the transcript-binding polypeptides were functional components of the chloroplast transcriptional complex.
机译:我们已经使用光亲和标记来检查叶绿体RNA聚合酶成分,这些成分在质体DNA的体外转录过程中与新生的转录本接触。使用丰富的豌豆叶绿体RNA聚合酶制剂和含有质体16S rRNA启动子的重组质粒,在光敏类似物(4-硫代UTP)和α-32P-ATP存在下合成转录本。转录复合物的短暂照射使光敏新生RNA交联到近端蛋白质。转录复合物的标记依赖于4-硫基UTP和模板DNA。两个51和54 kDa的多肽始终与新生的转录本交联。交联RNA的总放射性的约60%与这些多肽有关。在一些实验中,还发现另外两个38 kDa和75 kDa的多肽分别与总交联RNA放射性的约13%和17%相关。紫外线交联的转录复合物对DNase或S1核酸酶水解均稳定,但对RNase T1部分敏感。该复合物对用RNase H水解的不敏感性表明新生的转录本未与模板交联。该复合物也可以被蛋白酶K和嗜热菌素水解。合成后向聚合酶制剂中添加含有4-硫代UMP残基的标记RNA分子时,未观察到交联。这表明该方法仅鉴定了在其合成过程中与转录本紧密接触的那些多肽。针对RNA-蛋白质复合物的抗体在Western blots上证实了叶绿体RNA聚合酶制剂中多肽的存在。这些抗体与叶绿体RNA聚合酶的预孵育抑制了质体DNA转录。这些数据表明,转录物结合多肽是叶绿体转录复合物的功能成分。

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