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

期刊

EXPERIMENTAL CELL RESEARCH
卷 303, 期 2, 页码 343-359

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ELSEVIER INC
DOI: 10.1016/j.yexcr.2004.10.001

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3T3-L1; Balb/c 14; dlk; Notch1; CSL/RBP-Jk/CBF-1; luciferase; yeast two-hybrid system

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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 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 Notch 1 activation, diminishes in confluent Balb/c14 cells transected 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. The-se 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. (C) 2004 Elsevier Inc. All rights reserved.

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