 |
|||||
|
|||||
|
|||||
|
|||||
|
|||||
Previous Article | Next Article
The Journal of Neuroscience, May 15, 2001, 21(10):3350-3359
The Neuronal Microtubule-Associated Protein 1B Is under Homeoprotein Transcriptional Control
María Luz Montesinos1, Isabelle Foucher1, Marcus Conradt1, Gaëll Mainguy1, Laurence Robel1, Alain Prochiantz1, and Michel Volovitch1, 2 1 Centre Nationale de la Recherche Scientifique Unité Mixte de Recherche 8542, Ecole Normale Supérieure, 75230 Paris, Cedex 05 France, and 2 University Paris 7, Unité de Formation et de Recherche de Biologie, 75005 Paris, France
To identify genes regulated by homeoprotein transcription factors in postnatal neurons, the DNA-binding domain (homeodomain) of Engrailed homeoprotein was internalized into rat cerebellum neurons. The internalized homeodomain (EnHD) acts as a competitive inhibitor of Engrailed and of several homeoproteins (Mainguy et al., 2000). Analysis by differential display revealed that microtubule-associated protein 1B (MAP1B) mRNA is upregulated by EnHD. This upregulation does not require protein synthesis, suggesting a direct effect of the homeodomain on MAP1B transcription. The promoter region of MAP1B was cut into several subdomains, and each subdomain was tested for its ability to bind Engrailed and EnHD and to associate with Engrailed-containing cerebellum nuclear extracts. In addition, the activity, and regulation by Engrailed, of each subdomain and of the entire promoter were evaluated in vivo by electroporation in the chick embryo neural tube. These experiments demonstrate that MAP1B promoter is regulated by Engrailed in vivo. Moreover, they show that one promoter domain that contains all ATTA homeoprotein cognate binding sites common to the rat and human genes is an essential element of this regulation. It is thus proposed that MAP1B, a cytoskeleton protein involved in neuronal growth and regeneration, is under homeoprotein transcriptional regulation.
Key words: neuronal morphogenesis; cytoskeleton; MAP1B; transcriptional targets; homeoproteins; engrailed; in vivo electroporation; differential display
Copyright © 2001 Society for Neuroscience 0270-6474/01/21103350-10$05.00/0
This article has been cited by other articles:
L. Zhao, L. Ku, Y. Chen, M. Xia, P. LoPresti, and Y. Feng
QKI Binds MAP1B mRNA and Enhances MAP1B Expression during Oligodendrocyte Development
Mol. Biol. Cell, October 1, 2006; 17(10): 4179 - 4186.
[Abstract] [Full Text] [PDF]
C. Southwood, C. He, J. Garbern, J. Kamholz, E. Arroyo, and A. Gow
CNS Myelin Paranodes Require Nkx6-2 Homeoprotein Transcriptional Activity for Normal Structure
J. Neurosci., December 15, 2004; 24(50): 11215 - 11225.
[Abstract] [Full Text] [PDF]
R. Lu, H. Wang, Z. Liang, L. Ku, W. T. O'Donnell, W. Li, S. T. Warren, and Y. Feng
The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development
PNAS, October 19, 2004; 101(42): 15201 - 15206.
[Abstract] [Full Text] [PDF]
I. Foucher, M. L. Montesinos, M. Volovitch, A. Prochiantz, and A. Trembleau
Joint regulation of the MAP1B promoter by HNF3{beta}/Foxa2 and Engrailed is the result of a highly conserved mechanism for direct interaction of homeoproteins and Fox transcription factors
Development, May 1, 2003; 130(9): 1867 - 1876.
[Abstract] [Full Text] [PDF]
A. Nakayama, H. Murakami, N. Maeyama, N. Yamashiro, A. Sakakibara, N. Mori, and M. Takahashi
Role for RFX Transcription Factors in Non-neuronal Cell-specific Inactivation of the Microtubule-associated Protein MAP1A Promoter
J. Biol. Chem., January 3, 2003; 278(1): 233 - 240.
[Abstract] [Full Text] [PDF]
I. Foucher, M. Volovitch, M. Frain, J. J. Kim, J.-C. Souberbielle, L. Gan, T. G. Unterman, A. Prochiantz, and A. Trembleau
Hoxa5 overexpression correlates with IGFBP1 upregulation and postnatal dwarfism: evidence for an interaction between Hoxa5 and Forkhead box transcription factors
Development, September 1, 2002; 129(17): 4065 - 4074.
[Abstract] [Full Text] [PDF]
|
|
|
|
 |
|