Human Mitochondrial Transcription Initiation Complexes Have Similar Topology on the Light and Heavy Strand Promoters

被引:18
作者
Morozov, Yaroslav I. [1 ]
Temiakov, Dmitry [1 ]
机构
[1] Rowan Univ, Sch Osteopath Med, Dept Cell Biol, Stratford, NJ 08084 USA
基金
美国国家卫生研究院;
关键词
mitochondrial DNA (mtDNA); promoter; protein cross-linking; RNA polymerase; transcription; transcription factor; LSP; TFAM; TFB2M; mtRNAP; RNA-POLYMERASE; REGULATORY ELEMENTS; DNA;
D O I
10.1074/jbc.C116.727966
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription is a highly regulated process in all domains of life. In human mitochondria, transcription of the circular genome involves only two promoters, called light strand promoter (LSP) and heavy strand promoter (HSP), located in the opposite DNA strands. Initiation of transcription occurs upon sequential assembly of an initiation complex that includes mitochondrial RNA polymerase (mtRNAP) and the initiation factors mitochondrial transcription factor A (TFAM) and TFB2M. It has been recently suggested that the transcription initiation factor TFAM binds to HSP and LSP in opposite directions, implying that the mechanisms of transcription initiation are drastically dissimilar at these promoters. In contrast, we found that binding of TFAM to HSP and the subsequent recruitment of mtRNAP results in a pre-initiation complex that is remarkably similar in topology and properties to that formed at the LSP promoter. Our data suggest that assembly of the pre-initiation complexes on LSP and HSP brings these transcription units in close proximity, providing an opportunity for regulatory proteins to simultaneously control transcription initiation in both mtDNA strands.
引用
收藏
页码:13432 / 13435
页数:4
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