LEPREL1, a novel ER and Golgi resident member of the Leprecan family

Biochem Biophys Res Commun. 2004 Apr 30;317(2):342-51. doi: 10.1016/j.bbrc.2004.03.060.

Abstract

We have identified a novel protein, Leprecan-like 1 (LEPREL1), with profound similarity to the Leprecan family of proteoglycans. The genomic organization of the Leprecan gene family was found to be highly conserved. Expression analysis shows that LEPREL1 is expressed in most tissues as a 3.4 kb transcript encoding an 80 kDa protein. A LEPREL1 specific antibody stains many cell types including adipocytes and neuroendocrine cells of the gastrointestinal epithelium. Muscle tissue contains a specific 6.5 kb transcript and a 200 kDa protein. The 3.4 kb LEPREL1 transcript encodes a 708 amino acid protein containing a signal sequence, four tetratricopeptide repeats (TPRs), a leucine zipper, a P-loop, a prolyl 4-hydroxylase alpha domain (P4Halpha), and a C-terminal KDEL ER-retention motif. LEPREL1 is localized to the ER and Golgi network and over-expressing it affects normal protein disulfide isomerase staining patterns in the ER.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Line, Tumor
  • Endoplasmic Reticulum / metabolism*
  • Endoplasmic Reticulum / ultrastructure
  • Fibrosarcoma / genetics
  • Fibrosarcoma / metabolism*
  • Golgi Apparatus / metabolism*
  • Golgi Apparatus / ultrastructure
  • Humans
  • Membrane Glycoproteins / chemistry*
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Molecular Sequence Data
  • Organ Specificity
  • Prolyl Hydroxylases
  • Proteoglycans / chemistry*
  • Proteoglycans / genetics
  • Proteoglycans / metabolism*
  • Sequence Analysis, Protein*
  • Sequence Homology, Amino Acid*
  • Species Specificity
  • Tissue Distribution

Substances

  • Lepre1 protein, mouse
  • Membrane Glycoproteins
  • Proteoglycans
  • Prolyl Hydroxylases
  • P3H1 protein, human