Giese A, Thalheim C, Brennicke A, Binder S
Allgemeine Botanik, Universität Ulm, Ulm, Germany.
Mol Gen Genet. 1996 Sep 25;252(4):429-36. doi: 10.1007/BF02173008.
Transcription initiation sites for the mitochondrial 18S rRNA genes in the dicot plants Arabidopsis thaliana, potato and pea were identified by a combination of in vitro capping, primer extension and S-1 analyses. These promoters contain a nonanucleotide motif and an AT-rich sequence similar to many mRNA and tRNA promoters in dicot mitochondria. In Arabidopsis and potato, active promoters are located within 120 nucleotides upstream of the 18S rRNA genes, as in Oenothera. The nucleotide sequence in the corresponding region in pea mitochondria is well conserved, but is not used as promoter in this plant. Instead a novel promoter sequence is used that lies several hundred nucleotides upstream. These results show that rRNAs can be transcribed from the same promoter types as mRNAs and tRNAs in plant mitochondria. However, the sequence features presently attributed to plant mitochondrial promoters-the conserved nonanucleotide and the upstream AT-rich box-do not allow to deduce the presence of an active promoter from genomic sequence data alone.
通过体外加帽、引物延伸和S-1分析相结合的方法,确定了双子叶植物拟南芥、马铃薯和豌豆中线粒体18S rRNA基因的转录起始位点。这些启动子含有一个九核苷酸基序和一个富含AT的序列,类似于双子叶植物线粒体中的许多mRNA和tRNA启动子。在拟南芥和马铃薯中,活性启动子位于18S rRNA基因上游120个核苷酸内,如同月见草属植物一样。豌豆线粒体相应区域的核苷酸序列保守性良好,但在该植物中不被用作启动子。相反,使用了位于上游数百个核苷酸处的一个新的启动子序列。这些结果表明,在植物线粒体中,rRNA可以与mRNA和tRNA从相同类型的启动子转录而来。然而,目前归因于植物线粒体启动子的序列特征——保守的九核苷酸和上游富含AT的框——并不能仅从基因组序列数据推断出活性启动子的存在。