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THE TRANSCRIPTION FACTOR, EGR-1, IS RAPIDLY MODULATED IN RESPONSE TO RETINOIC ACID IN P19 EMBRYONAL CARCINOMA-CELLS
被引:41
作者
:
EDWARDS, SA
论文数:
0
引用数:
0
h-index:
0
机构:
LA JOLLA CANC RES FDN,10901 N TORREY PINES RD,LA JOLLA,CA 92037
EDWARDS, SA
DARLAND, T
论文数:
0
引用数:
0
h-index:
0
机构:
LA JOLLA CANC RES FDN,10901 N TORREY PINES RD,LA JOLLA,CA 92037
DARLAND, T
SOSNOWSKI, R
论文数:
0
引用数:
0
h-index:
0
机构:
LA JOLLA CANC RES FDN,10901 N TORREY PINES RD,LA JOLLA,CA 92037
SOSNOWSKI, R
SAMUELS, M
论文数:
0
引用数:
0
h-index:
0
机构:
LA JOLLA CANC RES FDN,10901 N TORREY PINES RD,LA JOLLA,CA 92037
SAMUELS, M
ADAMSON, ED
论文数:
0
引用数:
0
h-index:
0
机构:
LA JOLLA CANC RES FDN,10901 N TORREY PINES RD,LA JOLLA,CA 92037
ADAMSON, ED
机构
:
[1]
LA JOLLA CANC RES FDN,10901 N TORREY PINES RD,LA JOLLA,CA 92037
[2]
UNIV CALIF SAN DIEGO,CTR CANC,LA JOLLA,CA 92037
来源
:
DEVELOPMENTAL BIOLOGY
|
1991年
/ 148卷
/ 01期
关键词
:
D O I
:
10.1016/0012-1606(91)90327-Y
中图分类号
:
Q [生物科学];
学科分类号
:
07 ;
0710 ;
09 ;
摘要
:
The pluripotent murine embryonal carcinoma cell line, P19, differentiates along at least three main pathways under the inductive influence of retinoic acid (RA). The events most critical to the establishment of a particular differentiation pathway must occur early since P19 cells are committed to differentiation pathways after 30 min of exposure to RA (M. W. McBurney, personal communication and our unpublished results). We have, therefore, looked for genes that are induced (or repressed) within 30 min of RA addition and find that Egr-1 is one of these genes. Egr-1 is a transcription factor of the zinc-finger class and is known to transactivate genes after binding to specific oligonucleotide sequences. We describe here the extremely rapid and transient increase of Egr-1 transcript and protein levels in P19 cells after RA addition. Stable induction of Egr-1 transcripts occurred in the presence of protein synthesis inhibitors. Simultaneous addition of RA and cycloheximide did not result in an additive effect. The mechanism of induction with either drug appears to involve relief of a block to transcriptional elongation. The response was more rapid at high RA concentrations and this suggests that the Egr-1 transcription factor could play a role in initiation of differentiation pathways of P19 EC cells. © 1991.
引用
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页码:165 / 173
页数:9
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共 47 条
[1]
PRODUCT OF THE CELLULAR ONCOGENE, C-FOS, OBSERVED IN MOUSE AND HUMAN-TISSUES USING AN ANTIBODY TO A SYNTHETIC PEPTIDE
ADAMSON, ED
论文数:
0
引用数:
0
h-index:
0
ADAMSON, ED
MEEK, J
论文数:
0
引用数:
0
h-index:
0
MEEK, J
EDWARDS, SA
论文数:
0
引用数:
0
h-index:
0
EDWARDS, SA
[J].
EMBO JOURNAL,
1985,
4
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-
947
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COMPLEXITY OF THE EARLY GENETIC RESPONSE TO GROWTH-FACTORS IN MOUSE FIBROBLASTS
ALMENDRAL, JM
论文数:
0
引用数:
0
h-index:
0
机构:
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
ALMENDRAL, JM
SOMMER, D
论文数:
0
引用数:
0
h-index:
0
机构:
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
SOMMER, D
MACDONALDBRAVO, H
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0
引用数:
0
h-index:
0
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EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
MACDONALDBRAVO, H
BURCKHARDT, J
论文数:
0
引用数:
0
h-index:
0
机构:
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
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PERERA, J
论文数:
0
引用数:
0
h-index:
0
机构:
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
PERERA, J
BRAVO, R
论文数:
0
引用数:
0
h-index:
0
机构:
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
EUROPEAN MOLEC BIOL LAB, D-6900 HEIDELBERG, GERMANY
BRAVO, R
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CELL-DENSITY AND CELL-CYCLE EFFECTS ON RETINOIC ACID-INDUCED EMBRYONAL CARCINOMA CELL-DIFFERENTIATION
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BERG, RW
MCBURNEY, MW
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HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV MED ONCOL,BOSTON,MA 02115
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KRAL, A
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CAO, XM
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0
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0
h-index:
0
机构:
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CAO, XM
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0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
KOSKI, RA
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机构:
UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
GASHLER, A
MCKIERNAN, M
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机构:
UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
MCKIERNAN, M
MORRIS, CF
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机构:
UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
MORRIS, CF
GAFFNEY, R
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机构:
UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
GAFFNEY, R
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引用数:
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h-index:
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机构:
UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
HAY, RV
SUKHATME, VP
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0
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UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
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0
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0
h-index:
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机构:
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ROCKEFELLER UNIV,CELL BIOL LAB,NEW YORK,NY 10021
CHEN, TA
ALLFREY, VG
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0
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0
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: 5252
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CHRISTY, BA
论文数:
0
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0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT MOLEC BIOL & GENET,BALTIMORE,MD 21205
JOHNS HOPKINS UNIV,SCH MED,DEPT MOLEC BIOL & GENET,BALTIMORE,MD 21205
CHRISTY, BA
LAU, LF
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT MOLEC BIOL & GENET,BALTIMORE,MD 21205
JOHNS HOPKINS UNIV,SCH MED,DEPT MOLEC BIOL & GENET,BALTIMORE,MD 21205
LAU, LF
NATHANS, D
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT MOLEC BIOL & GENET,BALTIMORE,MD 21205
JOHNS HOPKINS UNIV,SCH MED,DEPT MOLEC BIOL & GENET,BALTIMORE,MD 21205
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