Hereditary neutropenia: dogs explain human neutrophil elastase mutations.

Abstract

Mutations in ELA2, the gene encoding neutrophil elastase (NE), cause the human diseases cyclic neutropenia (CN) and severe congenital neutropenia (SCN). Numerous mutations are known, but their lack of consistent biochemical effect has proven puzzling. The recent finding that mutation of AP3B1, which encodes the beta subunit of adaptor protein complex 3 (AP3), is the cause of canine CN suggests a model for the molecular basis of hereditary neutropenias, involving the mistrafficking of NE: AP3 recognizes NE as a cargo protein, and their interaction implies that NE is a transmembrane protein. Computerized algorithms predict two NE transmembrane domains. Most CN mutations fall within predicted transmembrane domains and lead to excessive deposition of NE in granules, whereas SCN mutations usually disrupt the AP3 recognition sequence, resulting in excessive transport to the plasma membrane.

• Authors: Marshall Horwitz, Kathleen F Benson, Zhijun Duan, Feng-Qian Li, Richard E Person
• Journal: Trends in molecular medicine (Trends Mol Med) Vol. 10 Issue 4 Pg. 163-70 (Apr 2004) ISSN: 1471-4914 [Print] England
• PMID: 15059607 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., Review)

Chemical References

• AP3B1 protein, human
• Adaptor Protein Complex 3
• Adaptor Protein Complex beta Subunits
• Membrane Transport Proteins
• Leukocyte Elastase

Topics

• Adaptor Protein Complex 3
• Adaptor Protein Complex beta Subunits
• Animals
• Cell Membrane (metabolism)
• Disease Models, Animal
• Dogs
• Humans
• Leukocyte Elastase (genetics, metabolism)
• Membrane Transport Proteins (genetics)
• Models, Biological
• Models, Molecular
• Mutation
• Neutropenia (genetics)
• Protein Conformation
• Protein Structure, Tertiary
• Protein Transport
• Time Factors