Deficiency of carbohydrate response element-binding protein (ChREBP) reduces lipogenesis as well as glycolysis.

Abstract:

:The liver provides for long-term energy needs of the body by converting excess carbohydrate into fat for storage. Insulin is one factor that promotes hepatic lipogenesis, but there is increasing evidence that glucose also contributes to the coordinated regulation of carbohydrate and fat metabolism in liver by mechanisms that are independent of insulin. In this study, we show that the transcription factor, carbohydrate response element-binding protein (ChREBP), is required both for basal and carbohydrate-induced expression of several liver enzymes essential for coordinated control of glucose metabolism, fatty acid, and the synthesis of fatty acids and triglycerides in vivo.

authors

Iizuka K,Bruick RK,Liang G,Horton JD,Uyeda K

doi

10.1073/pnas.0401516101

keywords:

subject

Has Abstract

pub_date

2004-05-11 00:00:00

pages

7281-6

issue

19

eissn

0027-8424

issn

1091-6490

pii

0401516101

journal_volume

101

pub_type

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