Hübschmann T, Börner T
Department of Biology (Genetics), Humboldt-University Berlin, Germany.
Plant Mol Biol. 1998 Feb;36(3):493-6. doi: 10.1023/a:1005924502336.
Transcription of plastid genes in higher plants is driven by two RNA polymerases. One is encoded in the chloroplast, the other is encoded in the nucleus. RNA synthesis in ribosome-deficient plastids is performed exclusively by the nuclear-encoded enzyme. In vitro capping was used to identify the transcriptional start sites of the genes clpP and rpl23 in ribosome-free plastids of the barley mutant albostrians. No transcript initiation was found at sequences similar to eubacterial promoters. Instead, transcription started near the motif 5'-YRTA-3', which is also conserved in mitochondrial promoters of higher plants. Our data suggest that the nuclear encoded RNA polymerase is active in mature chloroplasts and is the sole polymerase involved in transcription of rpl123.
高等植物中质体基因的转录由两种RNA聚合酶驱动。一种由叶绿体编码,另一种由细胞核编码。核糖体缺陷型质体中的RNA合成仅由核编码酶进行。体外加帽用于鉴定大麦突变体白条纹叶中无核糖体质体中clpP和rpl23基因的转录起始位点。在与真细菌启动子相似的序列中未发现转录起始。相反,转录在基序5'-YRTA-3'附近开始,该基序在高等植物的线粒体启动子中也保守。我们的数据表明,核编码的RNA聚合酶在成熟叶绿体中具有活性,并且是参与rpl123转录的唯一聚合酶。