Genome-Wide Analysis Reveals Coating of the Mitochondrial Genome by TFAM

被引:37
|
作者
Wang, Yun E. [1 ]
Marinov, Georgi K. [1 ]
Wold, Barbara J. [1 ]
Chan, David C. [1 ,2 ]
机构
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
[2] CALTECH, Howard Hughes Med Inst, Pasadena, CA 91125 USA
来源
PLOS ONE | 2013年 / 8卷 / 08期
关键词
TRANSCRIPTION FACTOR-A; L-STRAND REPLICATION; DNA DAMAGE; CHIP-SEQ; OVEREXPRESSION; DYSFUNCTION; UPSTREAM; BINDING; ORIGIN; ACCUMULATION;
D O I
10.1371/journal.pone.0074513
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mitochondria contain a 16.6 kb circular genome encoding 13 proteins as well as mitochondrial tRNAs and rRNAs. Copies of the genome are organized into nucleoids containing both DNA and proteins, including the machinery required for mtDNA replication and transcription. The transcription factor TFAM is critical for initiation of transcription and replication of the genome, and is also thought to perform a packaging function. Although specific binding sites required for initiation of transcription have been identified in the D-loop, little is known about the characteristics of TFAM binding in its nonspecific packaging state. In addition, it is unclear whether TFAM also plays a role in the regulation of nuclear gene expression. Here we investigate these questions by using ChIP-seq to directly localize TFAM binding to DNA in human cells. Our results demonstrate that TFAM uniformly coats the whole mitochondrial genome, with no evidence of robust TFAM binding to the nuclear genome. Our study represents the first high-resolution assessment of TFAM binding on a genome-wide scale in human cells.
引用
收藏
页数:10
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