Published February 15, 2005 | Version v1
Journal article

dlk acts as a negative regulator of Notch1 activation through interactions with specific EGF-like repeats

  • 1. Biochemistry and Molecular Biology Branch, Department of Inorganic Chemistry, Organic Chemistry and Biochemistry, Medical School/RCBR, Regional Center for Biomedical Research, University of Castilla-La Mancha, Campus of Albacete, Avda. Almansa s/n, 02006 Albacete (Spain)
  • 2. Laboratory of Immunobiology, Division of Monoclonal Antibodies, Center for Biologics Evaluation and Research, Food and Drug Administration, Rockville, MD 20852 (United States)

Description

The protein dlk, encoded by the Dlk1 gene, belongs to the Notch epidermal growth factor (EGF)-like family of receptors and ligands, which participate in cell fate decisions during development. The molecular mechanisms by which dlk regulates cell differentiation remain unknown. By using the yeast two-hybrid system, we found that dlk interacts with Notch1 in a specific manner. Moreover, by using luciferase as a reporter gene under the control of a CSL/RBP-Jk/CBF-1-dependent promoter in the dlk-negative, Notch1-positive Balb/c 14 cell line, we found that addition of synthetic dlk EGF-like peptides to the culture medium or forced expression of dlk decreases endogenous Notch activity. Furthermore, the expression of the gene Hes-1, a target for Notch1 activation, diminishes in confluent Balb/c14 cells transfected with an expression construct encoding for the extracellular EGF-like region of dlk. The expression of Dlk1 and Notch1 increases in 3T3-L1 cells maintained in a confluent state for several days, which is associated with a concomitant decrease in Hes-1 expression. On the other hand, the decrease of Dlk1 expression in 3T3-L1 cells by antisense cDNA transfection is associated with an increase in Hes-1 expression. These results suggest that dlk functionally interacts in vivo with Notch1, which may lead to the regulation of differentiation processes modulated by Notch1 activation and signaling, including adipogenesis

Additional details

Identifiers

DOI
10.1016/j.yexcr.2004.10.001;
PII
S0014-4827(04)00582-8;

Publishing Information

Journal Title
Experimental Cell Research
Journal Volume
303
Journal Issue
2
Journal Page Range
p. 343-359
ISSN
0014-4827
CODEN
ECREAL

Optional Information

Copyright
Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.