TY - JOUR
T1 - Autophagy in protists
AU - Duszenko, Michael
AU - Ginger, Michael L.
AU - Brennand, Ana
AU - Gualdrón-López, Melisa
AU - Colombo, Maria Isabel
AU - Coombs, Graham H.
AU - Coppens, Isabelle
AU - Jayabalasingham, Bamini
AU - Langsley, Gordon
AU - De Castro, Solange Lisboa
AU - Menna-Barreto, Rubem
AU - Mottram, Jeremy C.
AU - Navarro, Miguel
AU - Rigden, Daniel J.
AU - Romano, Patricia S.
AU - Stoka, Veronika
AU - Turk, Boris
AU - Michels, Paul A.M.
PY - 2011/2/1
Y1 - 2011/2/1
N2 - Autophagy is the degradative process by which eukaryotic cells digest their own components using acid hydrolases within the lysosome. Originally thought to function almost exclusively in providing starving cells with nutrients taken from their own cellular constituents, autophagy is in fact involved in numerous cellular events including differentiation, turnover of macromolecules and organelles and defense against parasitic invaders. During the past 10-20 years, molecular components of the autophagic machinery have been discovered, revealing a complex interactome of proteins and lipids, which, in a concerted way, induce membrane formation to engulf cellular material and target it for lysosomal degradation. Here, our emphasis is autophagy in protists. We discuss experimental and genomic data indicating that the canonical autophagy machinery characterized in animals and fungi appeared prior to the radiation of major eukaryotic lineages. Moreover, we describe how comparative bioinformatics revealed that this canonical machinery has been subject to moderation, outright loss or elaboration on multiple occasions in protist lineages, most probably as a consequence of diverse lifestyle adaptations. We also review experimental studies illustrating how several pathogenic protists either utilize autophagy mechanisms or manipulate host-cell autophagy in order to establish or maintain infection within a host. The essentiality of autophagy for the pathogenicity of many parasites, and the unique features of some of the autophagy-related proteins involved, suggest possible new targets for drug discovery. Further studies of the molecular details of autophagy in protists will undoubtedly enhance our understanding of the diversity and complexity of this cellular phenomenon and the opportunities it offers as a drug target.
AB - Autophagy is the degradative process by which eukaryotic cells digest their own components using acid hydrolases within the lysosome. Originally thought to function almost exclusively in providing starving cells with nutrients taken from their own cellular constituents, autophagy is in fact involved in numerous cellular events including differentiation, turnover of macromolecules and organelles and defense against parasitic invaders. During the past 10-20 years, molecular components of the autophagic machinery have been discovered, revealing a complex interactome of proteins and lipids, which, in a concerted way, induce membrane formation to engulf cellular material and target it for lysosomal degradation. Here, our emphasis is autophagy in protists. We discuss experimental and genomic data indicating that the canonical autophagy machinery characterized in animals and fungi appeared prior to the radiation of major eukaryotic lineages. Moreover, we describe how comparative bioinformatics revealed that this canonical machinery has been subject to moderation, outright loss or elaboration on multiple occasions in protist lineages, most probably as a consequence of diverse lifestyle adaptations. We also review experimental studies illustrating how several pathogenic protists either utilize autophagy mechanisms or manipulate host-cell autophagy in order to establish or maintain infection within a host. The essentiality of autophagy for the pathogenicity of many parasites, and the unique features of some of the autophagy-related proteins involved, suggest possible new targets for drug discovery. Further studies of the molecular details of autophagy in protists will undoubtedly enhance our understanding of the diversity and complexity of this cellular phenomenon and the opportunities it offers as a drug target.
KW - Apicomplexa
KW - Autophagy
KW - Drug discovery
KW - Evolution
KW - Free-living protist
KW - Life-cycle differentiation
KW - Parasitic protist
KW - Pexophagy
KW - Trypanosomatidae
KW - Ubiquitination
UR - http://www.scopus.com/inward/record.url?scp=79551573171&partnerID=8YFLogxK
U2 - 10.4161/auto.7.2.13310
DO - 10.4161/auto.7.2.13310
M3 - Review article
C2 - 20962583
AN - SCOPUS:79551573171
VL - 7
SP - 127
EP - 158
JO - Autophagy
JF - Autophagy
SN - 1554-8627
IS - 2
ER -