Evolutionary duplication of a hepatic control region in the human apolipoprotein E gene locus. Identification of a second region that confers high level and liver-specific expression of the human apolipoprotein E gene in transgenic mice

J Biol Chem. 1995 Nov 3;270(44):26278-81. doi: 10.1074/jbc.270.44.26278.

Abstract

We have identified a second hepatic control region (HCR-2) in the human apolipoprotein (apo) E gene locus that confers liver expression of the human apoE gene in transgenic mice. This HCR-2 sequence is located 27 kilobases downstream of the apoE gene and 10 kilobases downstream of the previously described liver-specific enhancer (HCR-1). Nucleotide sequence analysis of the HCR-2 region revealed a sequence that shares 85% identity to the functional 319-base pair domain of HCR-1. To test its activity, transgenic mice were prepared with a fusion construct containing a human apoE gene fragment, which is not normally expressed in the liver, ligated to a 632-base pair region containing the HCR-2 sequence. This construct resulted in high levels of liver-specific apoE transgene expression, indicating that HCR-2 can function as a hepatic enhancer and has an activity similar to that of HCR-1. Hence, these findings suggest that there are at least two hepatic control regions, HCR-1 and HCR-2, capable of controlling the liver expression of this human apolipoprotein gene locus.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Apolipoproteins E / genetics*
  • Base Sequence
  • Biological Evolution*
  • Cloning, Molecular
  • Consensus Sequence
  • Gene Expression Regulation*
  • Genome, Human
  • Hominidae / genetics*
  • Humans
  • Liver / metabolism*
  • Mice
  • Mice, Transgenic
  • Molecular Sequence Data
  • Multigene Family*
  • Organ Specificity
  • RNA, Messenger / analysis
  • RNA, Messenger / biosynthesis
  • Regulatory Sequences, Nucleic Acid*
  • Restriction Mapping
  • Sequence Homology, Nucleic Acid

Substances

  • Apolipoproteins E
  • RNA, Messenger