Chang D D, Clayton D A
Proc Natl Acad Sci U S A. 1985 Jan;82(2):351-5. doi: 10.1073/pnas.82.2.351.
Individual promoters for transcription of each strand of human mtDNA are located near the origin of heavy-strand DNA replication in the displacement-loop region. Initiation of heavy-strand synthesis represents the first event in mtDNA replication. Analyses of the 5' and 3' map positions of displacement-loop nucleic acids from mitochondria of cultured human cells reveal a close correspondence between the 3' ends of RNA, whose 5' ends map at a unique site, and the 5' ends of DNA strands. The 5' ends of the RNA species all map at nucleotide position 407 in the genomic sequence, which corresponds exactly to the major 5' transcriptional start site, determined previously in vitro, that is contained within the light-strand promoter sequence. Displacement-loop heavy-strand DNAs map immediately adjacent to the 3' termini of these RNAs, and these transition points between RNA and DNA lie within short conserved sequence blocks in the template sequence. The simplest interpretation of these data is that replication is initiated at the major transcriptional promoter with subsequent precise cleavage of primary transcripts to provide the appropriate primer species.
人类线粒体DNA(mtDNA)每条链转录的个别启动子位于置换环区域重链DNA复制起点附近。重链合成的起始是mtDNA复制的首个事件。对培养的人类细胞线粒体置换环核酸的5'和3'图谱位置分析显示,RNA的3'末端(其5'末端位于一个独特位点)与DNA链的5'末端之间存在紧密对应关系。RNA种类的5'末端均位于基因组序列的核苷酸位置407处,这恰好对应于先前在体外确定的主要5'转录起始位点,该位点包含在轻链启动子序列内。置换环重链DNA紧邻这些RNA的3'末端定位,RNA与DNA之间的这些转换点位于模板序列中的短保守序列块内。对这些数据最简单的解释是,复制在主要转录启动子处起始,随后对初级转录本进行精确切割以提供合适的引物种类。