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Mammalian patatin domain containing proteins: a family with diverse lipolytic activities involved in multiple biological functions

Authors :
Petra C. Kienesberger
Monika Oberer
Achim Lass
Rudolf Zechner
Source :
Journal of Lipid Research, Vol 50, Iss , Pp S63-S68 (2009)
Publication Year :
2009
Publisher :
Elsevier, 2009.

Abstract

The human genome expresses nine patatin-like phospholipase domain containing proteins (PNPLA1–9). Members of this family share a protein domain discovered initially in patatin, the most abundant protein of the potato tuber. Patatin is a lipid hydrolase with an unusual folding topology that differs from classical lipases. Mammalian PNPLAs include lipid hydrolases with specificities for diverse substrates such as triacylglycerols, phospholipids, and retinol esters. Analysis of induced mutant mouse models and the clinical phenotype of patients with mutations revealed important insights into the physiological role of several members of the PNPLA family. This review aims to summarize current knowledge of PNPLA proteins and to document their emerging importance in lipid and energy homeostasis.

Details

Language :
English
ISSN :
00222275
Volume :
50
Issue :
S63-S68
Database :
Directory of Open Access Journals
Journal :
Journal of Lipid Research
Publication Type :
Academic Journal
Accession number :
edsdoj.f36259c59a5449f1bc77a6323cbc2cd6
Document Type :
article
Full Text :
https://doi.org/10.1194/jlr.R800082-JLR200