Identification and characterisation of a new human glucose-6-phosphatase isoform

FEBS Lett. 2003 Sep 11;551(1-3):159-64. doi: 10.1016/s0014-5793(03)00903-7.

Abstract

The liver endoplasmic reticulum glucose-6-phosphatase catalytic subunit (G6PC1) catalyses glucose 6-phosphate hydrolysis during gluconeogenesis and glycogenolysis. The highest glucose-6-phosphatase activities are found in the liver and the kidney; there have been many reports of glucose 6-phosphate hydrolysis in other tissues. We cloned a new G6Pase isoform (G6PC3) from human brain encoded by a six-exon gene (chromosome 17q21). G6PC3 protein was able to hydrolyse glucose 6-phosphate in transfected Chinese hamster ovary cells. The optimal pH for glucose 6-phosphate hydrolysis was lower and the K(m) higher relative to G6PC1. G6PC3 preferentially hydrolyzed other substrates including pNPP and 2-deoxy-glucose-6-phosphate compared to the liver enzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CHO Cells
  • Cloning, Molecular
  • Cricetinae
  • Gene Components
  • Glucose-6-Phosphatase / chemistry
  • Glucose-6-Phosphatase / genetics*
  • Glucose-6-Phosphatase / metabolism*
  • Humans
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Molecular Sequence Data
  • RNA, Messenger / metabolism
  • Sequence Alignment
  • Sequence Analysis, Protein
  • Substrate Specificity
  • Tissue Distribution

Substances

  • Isoenzymes
  • RNA, Messenger
  • Glucose-6-Phosphatase