Aloni Y, Attardi G
Proc Natl Acad Sci U S A. 1971 Aug;68(8):1757-61. doi: 10.1073/pnas.68.8.1757.
RNA.DNA hybridization experiments utilizing separated strands of HeLa mitochondrial DNA and mit-RNA from HeLa cells exposed to short pulses of [5-(3)H]uridine have shown that the labeled RNA hybridizes with both the light (L) and the heavy (H) strand, though to a different relative extent depending upon the labeling time. Thus, hybridization of pulse-labeled RNA is about equal with the two strands when the pulse is very short (1-5 min), and becomes more and more predominant with the H strand with increasing pulse length. Pulse-labeled fast-sedimenting mit-RNA forms RNase-resistant double-stranded structures up to more than 5 mum long when self-annealed or annealed with an excess of unlabeled mit-RNA. These observations and the previous evidence of complete transcription of the H strand strongly suggest that mit-DNA is transcribed in HeLa cells symmetrically over a considerable portion of its length, with the transcript of the L strand being rapidly degraded or otherwise removed from the mitochondrial fraction.
利用从暴露于短脉冲[5-(3)H]尿苷的海拉细胞中分离出的海拉线粒体DNA单链和线粒体RNA进行的RNA-DNA杂交实验表明,标记的RNA与轻链(L)和重链(H)均能杂交,不过根据标记时间的不同,相对杂交程度有所差异。因此,当脉冲时间非常短时(1-5分钟),脉冲标记的RNA与两条链的杂交程度大致相等,随着脉冲长度增加,与重链的杂交变得越来越占主导。脉冲标记的快速沉降线粒体RNA在自身退火或与过量未标记的线粒体RNA退火时,会形成长达5微米以上的抗核糖核酸酶双链结构。这些观察结果以及之前关于重链完全转录的证据有力地表明,线粒体DNA在海拉细胞中沿着其相当一部分长度进行对称转录,轻链转录本迅速降解或以其他方式从线粒体部分中去除。