The structure and biological function of CREG

Gaby Ghobrial, Luiz Araujo, Felecia Jinwala, Shaohua Li, Leonard Y. Lee

Research output: Contribution to journalReview articlepeer-review

20 Scopus citations

Abstract

The cellular repressor of E1A-stimulated genes (CREG) is a 220 amino acid glycoprotein structurally similar to oxidoreductases. However, CREG does not have enzymatic activities because it cannot bind to the cofactor flavin mononucleotide. Although CREG can be secreted, it is mainly an intracellular protein localized in the endocytic-lysosomal compartment. It undergoes proteolytic maturation mediated by lysosomal cysteine proteases. Biochemical studies have demonstrated that CREG interacts with mannose-6-phosphate/insulin-like growth factor-2 receptor (M6P/IGF2R) and exocyst Sec8. CREG inhibits proliferation and induces differentiation and senescence when overexpressed in cultured cells. In Drosophila, RNAi-mediated knockdown of CREG causes developmental lethality at the pupal stage. In mice, global deletion of the CREG1 gene leads to early embryonic death. These findings establish an essential role for CREG in development. CREG1 haploinsufficient and liver-specific knockout mice are susceptible to high fat diet-induced obesity, hepatic steatosis and insulin resistance. The purpose of this review is to provide an overview of what we know about the biochemistry and biology of CREG and to discuss the important questions that remain to be addressed in the future.

Original languageEnglish (US)
Article number136
JournalFrontiers in Cell and Developmental Biology
Volume6
Issue numberOCT
DOIs
StatePublished - Oct 26 2018

All Science Journal Classification (ASJC) codes

  • Developmental Biology
  • Cell Biology

Keywords

  • CREG
  • Differentiation
  • Exocyst
  • Lysosome
  • Mannose-6-phosphate/insulin-like growth factor-2 receptor
  • Metabolism
  • Proliferation

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