Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene family

Genomics. 2004 Mar;83(3):445-53. doi: 10.1016/j.ygeno.2003.08.019.


Several mammalian sialidases have been cloned so far and here we describe the identification and expression of a new member of the human sialidase gene family. The NEU4 gene, identified by searching sequence databases for entries showing homologies to the human cytosolic sialidase NEU2, maps in 2q37 and encodes a 484-residue protein. The polypeptide contains all the typical sialidase amino acid motifs and, apart from an amino acid stretch that appears unique among mammalian sialidases, shows a high degree of homology for NEU2 and the plasma membrane-associated (NEU3) sialidases. RNA dot-blot analysis showed a low but wide expression pattern, with the highest level in liver. Transient transfection in COS7 cells allowed the detection of a sialidase activity toward the artificial substrate 4MU-NeuAc in the acidic range of pH. Immunofluorescence staining and Western blot analysis demonstrated the association of NEU4 with the inner cell membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • COS Cells
  • Cloning, Molecular*
  • Fluorescent Antibody Technique
  • Genetic Vectors
  • Humans
  • Mice
  • Molecular Sequence Data
  • Neuraminidase / genetics*
  • Neuraminidase / metabolism
  • Plasmids
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Transfection


  • Recombinant Proteins
  • NEU4 protein, human
  • Neu4 protein, mouse
  • Neuraminidase

Associated data

  • OMIM/256550