Mitochondrial DNA Transcription and Its Regulation: An Evolutionary Perspective

被引:147
作者
Barshad, Gilad [1 ]
Marom, Shani [1 ]
Cohen, Tal [1 ]
Mishmar, Dan [1 ]
机构
[1] Ben Gurion Univ Negev, Dept Life Sci, IL-8410501 Beer Sheva, Israel
基金
美国国家科学基金会; 以色列科学基金会;
关键词
ELEMENT-BINDING PROTEIN; HEAVY-STRAND PROMOTER; TERMINATION FACTOR MTERF; D-LOOP REGION; RIBOSOMAL-RNA; GENE-EXPRESSION; INITIATION SITES; HUMAN MTDNA; PGC-1-RELATED COACTIVATOR; PRECISE ASSIGNMENT;
D O I
10.1016/j.tig.2018.05.009
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The bacterial heritage of mitochondria, as well as its independent genome [mitochondrial DNA (mtDNA)] and polycistronic transcripts, led to the view that mitochondrial transcriptional regulation relies on an evolutionarily conserved, prokaryotic-like system that is separated from the rest of the cell. Indeed, mtDNA transcription was previously thought to be governed by a few dedicated direct regulators, namely, the mitochondrial RNA polymerase (POLRMT), two transcription factors (TFAM and TF2BM), one transcription elongation (TEFM), and one known transcription termination factor (mTERF1). Recent findings have, however, revealed that known nuclear gene expression regulators are also involved in mtDNA transcription and have identified novel transcriptional features consistent with adaptation of the mitochondria to the regulatory environment of the precursor of the eukaryotic cell. Finally, whereas mammals follow the human mtDNA transcription pattern, other organisms notably diverge in terms of mtDNA transcriptional regulation. Hence, mtDNA transcriptional regulation is likely more evolutionary diverse than once thought.
引用
收藏
页码:682 / 692
页数:11
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