help button home button Endocrine Society Molecular Endocrinology ENDO 08 Sessions Library
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by DeFranco, C.
Right arrow Articles by Wagner, J. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by DeFranco, C.
Right arrow Articles by Wagner, J. A.

Molecular Endocrinology, Vol 7, 365-379, Copyright © 1993 by Endocrine Society


ARTICLES

Nerve growth factor induces transcription of NGFIA through complex regulatory elements that are also sensitive to serum and phorbol 12- myristate 13-acetate

C DeFranco, DH Damon, M Endoh and JA Wagner
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts.

The expression of NGFIA (also known as egr1, zif268, TIS8, krox24, and d2) is rapidly and transiently increased by nerve growth factor (NGF) in PC12 cells. The 5'-region of this gene includes four serum response elements (SREs), a cAMP-like response element, an AP1-like response element, and an SP1-binding site. From deletion analysis of chloramphenicol acetyltransferase reporter constructs, we have established that the first 106 basepairs 5' of the transcriptional start site are sufficient for induction of NGFIA by NGF in PC12 cells; deletion beyond this point results in dramatically reduced induction of the gene. Using defined mutations in the NGFIA promoter and NGFIA- thymidine kinase hybrid promoters, we have defined three elements (SRE1, SRE2, and AP1-like) in the first 106 basepairs of upstream DNA, each of which contributes to induction of NGFIA by NGF. Cooperation by two of these elements (i.e. the two SREs or one SRE and the AP1-like element) is sufficient to confer transcriptional induction by NGF, but the combination of all three elements increased induction by NGF more effectively than a pair of elements. This suggests that the response of NGFIA to NGF is mediated by a cis-acting sequence that is composed of at least three distinct elements. An oligonucleotide composed of SRE1 and SRE2 that can confer the ability for NGF induction to heterologous promoter constructs complexes with proteins in PC12 cell nuclear extracts, but the protein-DNA complexes do not appear to be altered by NGF treatment, as measured by DNA mobility shift assays. We have also established that the regulatory region of NGFIA that mediates NGF induction also mediates the induction by serum and phorbol 12-myristate 13-acetate, suggesting that multiple signal transduction pathways must converge on these sequences to regulate the expression of this gene.


This article has been cited by other articles:


Home page
J. Neurosci.Home page
S. A. Pintchovski, C. L. Peebles, H. Joo Kim, E. Verdin, and S. Finkbeiner
The Serum Response Factor and a Putative Novel Transcription Factor Regulate Expression of the Immediate-Early Gene Arc/Arg3.1 in Neurons
J. Neurosci., February 4, 2009; 29(5): 1525 - 1537.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
F. Marampon, M. C. Casimiro, M. Fu, M. J. Powell, V. M. Popov, J. Lindsay, B. M. Zani, C. Ciccarelli, G. Watanabe, R. J. Lee, et al.
Nerve Growth Factor Regulation of Cyclin D1 in PC12 Cells through a p21RAS Extracellular Signal-regulated Kinase Pathway Requires Cooperative Interactions between Sp1 and Nuclear Factor-{kappa}B
Mol. Biol. Cell, June 1, 2008; 19(6): 2566 - 2578.
[Abstract] [Full Text] [PDF]


Home page
Mol Cancer ResHome page
G. R. Mora, K. R. Olivier, J. C. Cheville, R. F. Mitchell Jr., W. L. Lingle, and D. J. Tindall
The Cytoskeleton Differentially Localizes the Early Growth Response Gene-1 Protein in Cancer and Benign Cells of the Prostate
Mol. Cancer Res., February 1, 2004; 2(2): 115 - 128.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
H. Xi and G. J. Kersh
Induction of the Early Growth Response Gene 1 Promoter by TCR Agonists and Partial Agonists: Ligand Potency Is Related to Sustained Phosphorylation of Extracellular Signal-Related Kinase Substrates
J. Immunol., January 1, 2003; 170(1): 315 - 324.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
W. R. Duan, M. Ito, Y. Park, E. T. Maizels, M. Hunzicker-Dunn, and J. L. Jameson
GnRH Regulates Early Growth Response Protein 1 Transcription Through Multiple Promoter Elements
Mol. Endocrinol., February 1, 2002; 16(2): 221 - 233.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. Zentrich, S.-Y. Han, L. Pessoa-Brandao, L. Butterfield, and L. E. Heasley
Collaboration of JNKs and ERKs in Nerve Growth Factor Regulation of the Neurofilament Light Chain Promoter in PC12 Cells
J. Biol. Chem., February 1, 2002; 277(6): 4110 - 4118.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. Farias-Eisner, L. Vician, A. Silver, S. Reddy, S. A. Rabbani, and H. R. Herschman
The Urokinase Plasminogen Activator Receptor (UPAR) Is Preferentially Induced by Nerve Growth Factor in PC12 Pheochromocytoma Cells and Is Required for NGF-Driven Differentiation
J. Neurosci., January 1, 2000; 20(1): 230 - 239.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
S. Etienne-Manneville, N. Chaverot, A. D. Strosberg, and P.-O. Couraud
ICAM-1-Coupled Signaling Pathways in Astrocytes Converge to Cyclic AMP Response Element-Binding Protein Phosphorylation and TNF-{alpha} Secretion
J. Immunol., July 15, 1999; 163(2): 668 - 674.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. J. Townsend, P. Zhou, L. Qian, C. K. Bieszczad, C. H. Lowrey, A. Yen, and R. W. Craig
Regulation of MCL1 through a Serum Response Factor/Elk-1-mediated Mechanism Links Expression of a Viability-promoting Member of the BCL2 Family to the Induction of Hematopoietic Cell Differentiation
J. Biol. Chem., January 15, 1999; 274(3): 1801 - 1813.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. M. Cohen, S. R. Gullans, and W. W. Chin
Urea Inducibility of egr-1 in Murine Inner Medullary Collecting Duct Cells Is Mediated by the Serum Response Element and Adjacent Ets Motifs
J. Biol. Chem., May 31, 1996; 271(22): 12903 - 12908.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. C. Reddy, S. Hosono, and J. D. Licht
The Transcriptional Effect of WT1 Is Modulated by Choice of Expression Vector
J. Biol. Chem., December 15, 1995; 270(50): 29976 - 29982.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
N. A. Papanikolaou and E. L. Sabban
Ability of Egr1 to Activate Tyrosine Hydroxylase Transcription in PC12 Cells. CROSS-TALK WITH AP-1 FACTORS
J. Biol. Chem., August 25, 2000; 275(35): 26683 - 26689.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1993 by The Endocrine Society