Lippok B, Brennicke A, Wissinger B
Institut für Genbiologische Forschung, Berlin, Germany.
Mol Gen Genet. 1994 Apr;243(1):39-46. doi: 10.1007/BF00283874.
Introns a/b of the nad2 gene and b/c of the nad1 gene in Oenothera mitochondria were found to be closely related. Within a scaffold of conserved sequence regions, a 48 bp sequence element covering intron domain V and flanking nucleotides is identical in both group II introns. The third nucleotide of this element is edited in the nad2, but not in the nad1 intervening sequence. The C to U editing event compensates an nad2-specific nucleotide mismatch in the stem domain IV and thus improves secondary structure stability. This differential editing event indicates that the identical upstream 2 and downstream 45 nucleotides are not sufficient to specify this editing site. Comparison of adjacent exon editing patterns in spliced and unspliced transcripts shows a higher degree of editing in processed sequences, confirming that RNA editing is a posttranscriptional process in plant mitochondria.
月见草线粒体中nad2基因的内含子a/b和nad1基因的内含子b/c被发现密切相关。在保守序列区域的一个支架内,覆盖内含子结构域V和侧翼核苷酸的48个碱基对的序列元件在两个II类内含子中是相同的。该元件的第三个核苷酸在nad2中被编辑,但在nad1的间隔序列中未被编辑。C到U的编辑事件补偿了茎结构域IV中nad2特异性的核苷酸错配,从而提高了二级结构稳定性。这种差异编辑事件表明,相同的上游2个和下游45个核苷酸不足以指定这个编辑位点。对剪接和未剪接转录本中相邻外显子编辑模式的比较表明,加工后的序列中有更高程度的编辑,证实了RNA编辑是植物线粒体中的一个转录后过程。