Mechanisms of mammalian mitochondrial transcription

被引:27
作者
Bouda, Emilie [1 ]
Stapon, Anthony [1 ]
Garcia-Diaz, Miguel [1 ]
机构
[1] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
基金
美国国家科学基金会;
关键词
mitochondrial transcription; mitochondrial gene expression; POLRMT; TEFM; MTERF1; TFAM; TFB2M; mitochondrial RNA processing; TERMINATION FACTOR MTERF; ELEMENT-BINDING PROTEIN; HEAVY-STRAND PROMOTER; CCA-ADDING ENZYME; RNA-POLYMERASE; HUMAN MTDNA; HELA-CELLS; METHYLTRANSFERASE ACTIVITY; PGC-1-RELATED COACTIVATOR; PRECISE ASSIGNMENT;
D O I
10.1002/pro.3688
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
Numerous age-related human diseases have been associated with deficiencies in cellular energy production. Moreover, genetic alterations resulting in mitochondrial dysfunction are the cause of inheritable disorders commonly known as mitochondrial diseases. Many of these deficiencies have been directly or indirectly linked to deficits in mitochondrial gene expression. Transcription is an essential step in gene expression and elucidating the molecular mechanisms involved in this process is critical for understanding defects in energy production. For the past five decades, substantial efforts have been invested in the field of mitochondrial transcription. These efforts have led to the discovery of the main protein factors responsible for transcription as well as to a basic mechanistic understanding of the transcription process. They have also revealed various mechanisms of transcriptional regulation as well as the links that exist between the transcription process and downstream processes of RNA maturation. Here, we review the knowledge gathered in early mitochondrial transcription studies and focus on recent findings that shape our current understanding of mitochondrial transcription, posttranscriptional processing, as well as transcriptional regulation in mammalian systems.
引用
收藏
页码:1594 / 1605
页数:12
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