Inositol lipids: From an archaeal origin to phosphatidylinositol 3,5-bisphosphate faults in human disease

Research output: Contribution to journalReview article

Authors

Colleges, School and Institutes

Abstract

The last couple of decades have seen an extraordinary transformation in our knowledge and understanding of the multifarious biological roles of inositol phospholipids. Herein, I briefly consider two topics. The first is the role that recently acquired biochemical and genomic information - especially from archaeons - has played in illuminating the possible evolutionary origins of the biological employment of inositol in lipids, and some questions that these studies raise about the 'classical' biosynthetic route to phosphatidylinositol. The second is the growing recognition of the importance in eukaryotic cells of phosphatidylinositol 3,5-bisphosphate. Phosphatidylinositol 3,5-bisphosphate only entered our phosphoinositide consciousness quite recently, but it is speedily gathering a plethora of roles in diverse cellular processes and diseases thereof. These include: control of endolysosomal vesicular trafficking and of the activity of ion channels and pumps in the endolysosomal compartment; control of constitutive and stimulated protein traffic to and from plasma membrane subdomains; control of the nutrient and stress-sensing target of rapamycin complex 1 pathway (TORC1); and regulation of key genes in some central metabolic pathways. I consider two topics. First, did inositol phospholipids originate in an archaeal ancestor of eukaryotes, and is their unexpected biosynthesis therein really unique? Second, what are the regulatory roles of PtdIns(3,5)P2 in eukaryotes? These seem to include influence over endolysosomal vesicular trafficking and ion homeostasis, plasma membrane protein trafficking, the TORC1 pathway and gene expression in central carbohydrate pathways.

Details

Original languageEnglish
Pages (from-to)6281-6294
Number of pages14
JournalFEBS Journal
Volume280
Issue number24
Publication statusPublished - 1 Dec 2013

Keywords

  • actinobacteria, endolysosome, Fab1, Vac14, vacuole acidification