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PMID: 16890538 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Carbohydrate response element binding protein, ChREBP, a transcription factor coupling hepatic glucose utilization and lipid synthesis.

Cell metabolism ·Vol. 4 ·No. 2 ·2006-08-00 ·Pages 107-10

Uyeda K, Repa JJ

Abstract

The ability of an organism to sense and store nutrients is vital to survival. The liver is the major organ responsible for converting excess dietary carbohydrate to lipid for storage. An elegant molecular pathway has evolved that allows increased glucose flux into hepatocytes to generate a signaling molecule, xylulose 5-phosphate, that triggers rapid changes in glycolytic enzyme activities and nuclear import of a transcription factor, ChREBP, which coordinates the transcriptional regulation of enzymes that channel the glycolytic end-products into lipogenesis. Further understanding of this metabolic cascade should provide insights on conditions such as fatty liver, obesity, and the metabolic syndrome.

MeSH Terms
Animals Basic Helix-Loop-Helix Leucine Zipper Transcription Factors Glucose/metabolism Humans Lipids/biosynthesis Liver/metabolism Nuclear Proteins/chemistry,genetics,physiology Signal Transduction Transcription Factors/chemistry,genetics,physiology
Chemicals
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors Lipids Mlxipl protein, mouse Nuclear Proteins Transcription Factors Glucose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Uyeda Kosaku
Dallas Veterans Affairs Medical Center, Dallas, Texas 75390, USA. [email protected]
Repa Joyce J
Article Info
Journal
Cell metabolism
Abbr.
Cell Metab
ISSN
1550-4131
Published
2006-08-00
Pages
107-10
Language
English
Region
United States
NLM ID
101233170
Subset
IM
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