SUMOylation of Krüppel-like transcription factor 5 acts as a molecular switch in transcriptional programs of lipid metabolism involving PPAR-delta

Nat Med. 2008 Jun;14(6):656-66. doi: 10.1038/nm1756. Epub 2008 May 25.

Abstract

Obesity and metabolic syndrome are increasingly recognized as major risk factors for cardiovascular disease. Herein we show that Krüppel-like transcription factor 5 (KLF5) is a crucial regulator of energy metabolism. Klf5(+/-) mice were resistant to high fat-induced obesity, hypercholesterolemia and glucose intolerance, despite consuming more food than wild-type mice. This may in part reflect their enhanced energy expenditure. Expression of the genes involved in lipid oxidation and energy uncoupling, including those encoding carnitine-palmitoyl transferase-1b (Cpt1b) and uncoupling proteins 2 and 3 (Ucp2 and Ucp3), was upregulated in the soleus muscles of Klf5(+/-) mice. Under basal conditions, KLF5 modified with small ubiquitin-related modifier (SUMO) proteins was associated with transcriptionally repressive regulatory complexes containing unliganded peroxisome proliferator-activated receptor-delta (PPAR-delta) and co-repressors and thus inhibited Cpt1b, Ucp2 and Ucp3 expression. Upon agonist stimulation of PPAR-delta, KLF5 was deSUMOylated, and became associated with transcriptional activation complexes containing both the liganded PPAR-delta and CREB binding protein (CBP). This activation complex increased the expression of Cpt1b, Ucp2 and Ucp3. Thus, SUMOylation seems to be a molecular switch affecting function of KLF5 and the transcriptional regulatory programs governing lipid metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Temperature
  • COS Cells
  • Cell Line
  • Chlorocebus aethiops
  • Cholesterol / blood
  • Crosses, Genetic
  • Genes, Reporter
  • Glucose Tolerance Test
  • Heterozygote
  • Kruppel-Like Transcription Factors / genetics
  • Kruppel-Like Transcription Factors / metabolism*
  • Leptin / blood
  • Lipid Metabolism*
  • Luciferases / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mutation
  • Myoblasts / cytology
  • Myoblasts / metabolism
  • Oxygen Consumption
  • PPAR delta / genetics
  • PPAR delta / metabolism*
  • Small Ubiquitin-Related Modifier Proteins / metabolism*
  • Transcription, Genetic*

Substances

  • Klf5 protein, mouse
  • Kruppel-Like Transcription Factors
  • Leptin
  • PPAR delta
  • Small Ubiquitin-Related Modifier Proteins
  • Cholesterol
  • Luciferases