HUMAN MITOCHONDRIAL TRANSCRIPTION FACTOR-A AND PROMOTER SPACING INTEGRITY ARE REQUIRED FOR TRANSCRIPTION INITIATION
被引:72
作者:
DAIRAGHI, DJ
论文数: 0引用数: 0
h-index: 0
机构:
STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305
DAIRAGHI, DJ
[1
]
SHADEL, GS
论文数: 0引用数: 0
h-index: 0
机构:
STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305
SHADEL, GS
[1
]
CLAYTON, DA
论文数: 0引用数: 0
h-index: 0
机构:
STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305
CLAYTON, DA
[1
]
机构:
[1] STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305
来源:
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
|
1995年
/
1271卷
/
01期
关键词:
TRANSCRIPTION;
TRANSCRIPTION FACTOR;
DNA BINDING PROTEIN;
D O I:
10.1016/0925-4439(95)00019-Z
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:
The two major promoters for transcription of the human mitochondrial genome are located near each other in the displacement-loop region of the molecule. Previous work has localized these promoters to regions of < 100 nucleotides each; the DNA sequence at the transcription start site is stringently required, as is the region from -10 to -40 base pairs upstream of each respective start site. Each upstream site is recognized and bound by human mitochondrial transcription factor A (h-mtTFA), an event previously shown to be important for transcriptional activation. We report here results using recombinant h-mtTFA that demonstrate the dependence of transcription initiation on h-mtTFA. In addition, altering the distance between the h-mtTFA binding site and the transcription start site greatly impairs transcription initiation efficiency. The decrease in transcription initiation efficiency was shown to be a consequence of altering the position of h-mtTFA binding as opposed to the strength of h-mtTFA binding, as judged by DNA footprinting ability. Analysis of a chimeric yeast-human promoter revealed that the yeast mtTFA homologue cannot substitute for the human protein, even when bound at an appropriate position upstream of the human transcription start site.