HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Interaction of Phospholipase A/Acyltransferase-3 with Pex19p: A POSSIBLE INVOLVEMENT IN THE DOWN-REGULATION OF PEROXISOMES.

Abstract
Phospholipase A/acyltransferase (PLA/AT)-3 (also known as H-rev107 or AdPLA) was originally isolated as a tumor suppressor and was later shown to have phospholipase A1/A2 activity. We have also found that the overexpression of PLA/AT-3 in mammalian cells results in specific disappearance of peroxisomes. However, its molecular mechanism remained unclear. In the present study, we first established a HEK293 cell line, which stably expresses a fluorescent peroxisome marker protein (DsRed2-Peroxi) and expresses PLA/AT-3 in a tetracycline-dependent manner. The treatment with tetracycline, as expected, caused disappearance of peroxisomes within 24 h, as revealed by diffuse signals of DsRed2-Peroxi and a remarkable decrease in a peroxisomal membrane protein, PMP70. A time-dependent decrease in ether-type lipid levels was also seen. Because the activation of LC3, a marker of autophagy, was not observed, the involvement of autophagy was unlikely. Among various peroxins responsible for peroxisome biogenesis, Pex19p functions as a chaperone protein for the transportation of peroxisomal membrane proteins. Immunoprecipitation analysis showed that PLA/AT-3 binds to Pex19p through its N-terminal proline-rich and C-terminal hydrophobic domains. The protein level and enzyme activity of PLA/AT-3 were increased by its coexpression with Pex19p. Moreover, PLA/AT-3 inhibited the binding of Pex19 to peroxisomal membrane proteins, such as Pex3p and Pex11βp. A catalytically inactive point mutant of PLA/AT-3 could bind to Pex19p but did not inhibit the chaperone activity of Pex19p. Altogether, these results suggest a novel regulatory mechanism for peroxisome biogenesis through the interaction between Pex19p and PLA/AT-3.
AuthorsToru Uyama, Katsuhisa Kawai, Nozomu Kono, Masahiro Watanabe, Kazuhito Tsuboi, Tomohito Inoue, Nobukazu Araki, Hiroyuki Arai, Natsuo Ueda
JournalThe Journal of biological chemistry (J Biol Chem) Vol. 290 Issue 28 Pg. 17520-34 (Jul 10 2015) ISSN: 1083-351X [Electronic] United States
PMID26018079 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2015 by The American Society for Biochemistry and Molecular Biology, Inc.
Chemical References
  • Lipoproteins
  • Membrane Proteins
  • PEX16 protein, human
  • Peroxins
  • Pex3 protein, human
  • Recombinant Proteins
  • Tumor Suppressor Proteins
  • PEX19 protein, human
  • PLAAT3 protein, human
  • Phospholipases A2, Calcium-Independent
Topics
  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • Down-Regulation
  • HEK293 Cells
  • Humans
  • Lipoproteins (chemistry, genetics, metabolism)
  • Membrane Proteins (chemistry, genetics, metabolism)
  • Models, Biological
  • Peroxins
  • Peroxisomes (metabolism)
  • Phospholipases A2, Calcium-Independent (chemistry, genetics, metabolism)
  • Protein Interaction Domains and Motifs
  • Recombinant Proteins (chemistry, genetics, metabolism)
  • Tumor Suppressor Proteins (chemistry, genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: