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RNA Polymerase Subunits Encoded by the Plastid rpo Genes Are Not Shared with the Nucleus-Encoded Plastid Enzyme

机译:质体rpo编码的RNA聚合酶亚基 基因不与核编码的质体共享 酵素

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摘要

Plastid genes in photosynthetic higher plants are transcribed by at least two RNA polymerases. The plastid rpoA, rpoB, rpoC1, and rpoC2 genes encode subunits of the plastid-encoded plastid RNA polymerase (PEP), an Escherichia coli-like core enzyme. The second enzyme is referred to as the nucleus-encoded plastid RNA polymerase (NEP), since its subunits are assumed to be encoded in the nucleus. Promoters for NEP have been previously characterized in tobacco plants lacking PEP due to targeted deletion of rpoB (encoding the β-subunit) from the plastid genome. To determine if NEP and PEP share any essential subunits, the rpoA, rpoC1, and rpoC2 genes encoding the PEP α-, β′-, and β"-subunits were removed by targeted gene deletion from the plastid genome. We report here that deletion of each of these genes yielded photosynthetically defective plants that lack PEP activity while maintaining transcription specificity from NEP promoters. Therefore, rpoA, rpoB, rpoC1, and rpoC2 encode PEP subunits that are not essential components of the NEP transcription machinery. Furthermore, our data indicate that no functional copy of rpoA, rpoB, rpoC1, or rpoC2 that could complement the deleted plastid rpo genes exists outside the plastids.
机译:光合高等植物中的质体基因被至少两种RNA聚合酶转录。质体rpoA,rpoB,rpoC1和rpoC2基因编码质体编码质体RNA聚合酶(PEP)(一种类似大肠杆菌的核心酶)的亚基。第二种酶被称为核编码的质体RNA聚合酶(NEP),因为假定其亚基在核中编码。先前已经在缺乏PEP的烟草植物中鉴定了NEP的启动子,这是由于从质体基因组中有针对性地删除了rpoB(编码β亚基)。为了确定NEP和PEP是否共享任何必需的亚基,通过从质体基因组中靶向性删除基因,删除了编码PEPα-,β'-和β“-亚基的rpoA,rpoC1和rpoC2基因。我们在此报告该缺失这些基因中的每一个产生的光合缺陷植物缺乏PEP活性,同时又保持了NEP启动子的转录特异性。 rpoB,rpoC1和rpoC2编码PEP 不是NEP转录必需成分的亚基 机械。此外,我们的数据表明,没有任何功能副本 rpoA,rpoB,rpoC1或 rpoC2可以补充缺失的质体 rpo基因存在于质体之外。

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