Mammalian transcription factor A is a core component of the mitochondrial transcription machinery

被引:148
作者
Shi, Yonghong [1 ,2 ]
Dierckx, Anke [3 ]
Wanrooij, Paulina H. [1 ,2 ]
Wanrooij, Sjoerd [1 ]
Larsson, Nils-Goran [2 ,4 ]
Wilhelmsson, L. Marcus [3 ]
Falkenberg, Maria [1 ]
Gustafsson, Claes M. [1 ]
机构
[1] Univ Gothenburg, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, Sweden
[2] Karolinska Inst, Div Metab Dis, S-17177 Stockholm, Sweden
[3] Chalmers Univ Technol, Dept Chem & Biol Engn Phys Chem, S-41296 Gothenburg, Sweden
[4] Max Planck Inst Biol Ageing, D-50931 Cologne, Germany
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
LIGHT-STRAND PROMOTER; RNA-POLYMERASE; YEAST MITOCHONDRIA; PRIMER FORMATION; DNA-REPLICATION; BASE ANALOG; IN-VITRO; FACTOR-A; PROTEIN; ACTIVATOR;
D O I
10.1073/pnas.1119738109
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
Transcription factor A (TFAM) functions as a DNA packaging factor in mammalian mitochondria. TFAM also binds sequence-specifically to sites immediately upstream of mitochondrial promoters, but there are conflicting data regarding its role as a core component of the mitochondrial transcription machinery. We here demonstrate that TFAM is required for transcription in mitochondrial extracts as well as in a reconstituted in vitro transcription system. The absolute requirement of TFAM can be relaxed by conditions that allow DNA breathing, i.e., low salt concentrations or negatively supercoiled DNA templates. The situation is thus very similar to that described in nuclear RNA polymerase II-dependent transcription, in which the free energy of supercoiling can circumvent the need for a subset of basal transcription factors at specific promoters. In agreement with these observations, we demonstrate that TFAM has the capacity to induce negative supercoils in DNA, and, using the recently developed nucleobase analog FRET-pair tC(O)-tC(nitro), we find that TFAM distorts significantly the DNA structure. Our findings differ from recent observations reporting that TFAM is not a core component of the mitochondrial transcription machinery. Instead, our findings support a model in which TFAM is absolutely required to recruit the transcription machinery during initiation of transcription.
引用
收藏
页码:16510 / 16515
页数:6
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