Calcium and growth factor pathways of c-fos transcriptional activation require distinct upstream regulatory sequences
Calcium and growth factor pathways of c-fos transcriptional activation require distinct upstream regulatory sequences
复制标题
c-fos转录激活的钙和生长因子途径需要不同的上游调控序列
DOI:
10.1128/mcb.8.7.2787-2796.1988
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发表时间:
1988
影响因子:
5.3
通讯作者:
Michael E. Greenberg
中科院分区:
文献类型:
--
作者:
M. Sheng;Scott T. Dougan;Grant McFadden;Michael E. Greenberg
Transcription of the c-fos proto-oncogene is rapidly induced in the rat pheochromocytoma PC12 cell line by a wide variety of stimuli, including polypeptide growth factors, phorbol esters, and calcium ion fluxes. We have mapped the upstream sequence requirements for this activation in PC12 cells by analysis of promoter deletion mutants in a transient expression assay. Two distinct pathways of c-fos induction are defined that differ in their requirement for cis-acting DNA sequences. Calcium activation of c-fos transcription is dependent on a DNA element located approximately 60 base pairs upstream of the transcription start site. This region is highly conserved between human, mouse, and chicken c-fos genes and contains a sequence that resembles the consensus for a cyclic AMP response element. The dyad symmetry element at position -300, which is necessary for serum responsiveness of c-fos, appears to be unimportant for calcium activation of the gene. The dyad symmetry element is, however, an essential cis-acting sequence for c-fos inducibility by nerve growth factor, epidermal growth factor, fibroblast growth factor, and the phorbol ester 12-O-tetradecanoyl phorbol-13-acetate. Studies in vivo and in vitro with various mutants of the dyad symmetry element indicate that c-fos activation by polypeptide growth factors and 12-O-tetradecanoyl activation by polypeptide growth factors and 12-O-tetradecanoyl phorbol-13-acetate is mediated by a common transcription factor, and that this factor is identical to the previously described serum response factor. In vitro DNA-binding assays suggest that the quantity of serum response factor-binding activity remains unchanged during c-fos transcriptional activation.
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DOI:
10.1016/s0021-9258(17)38689-1
发表时间:
1985-11
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
M. Greenberg;L. Greene;E. Ziff
通讯作者:
M. Greenberg;L. Greene;E. Ziff
DOI:
10.1073/pnas.83.18.6682
发表时间:
1986-09-01
影响因子:
11.1
作者:
MONTMINY, MR;SEVARINO, KA;GOODMAN, RH
通讯作者:
GOODMAN, RH
影响因子:
8
作者:
Kujubu,DA;Lim,RW;Varnum,BC;Herschman,HR
通讯作者:
Herschman,HR
影响因子:
56.9
作者:
GREENBERG, ME;ZIFF, EB;GREENE, LA
通讯作者:
GREENE, LA
DOI:
10.1073/pnas.81.23.7476
发表时间:
1984-01-01
期刊:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES
影响因子:
--
作者:
ELDER, PK;SCHMIDT, LJ;GETZ, MJ
通讯作者:
GETZ, MJ