The integration of autophagy and cellular trafficking pathways via RAB GAPs.
Andreas Kern, Ivan Dikic, Christian Behl
Author Information
Andreas Kern: a Institute for Pathobiochemistry; University Medical Center of the Johannes Gutenberg University ; Mainz , Germany.
Ivan Dikic: b Buchmann Institute for Molecular Life Sciences; Goethe University Frankfurt ; Frankfurt am Main , Germany.
Christian Behl: a Institute for Pathobiochemistry; University Medical Center of the Johannes Gutenberg University ; Mainz , Germany.
中文译文
English
Macroautophagy is a conserved degradative pathway in which a double-membrane compartment sequesters cytoplasmic cargo and delivers the contents to lysosomes for degradation. Efficient formation and maturation of autophagic vesicles, so-called phagophores that are precursors to autophagosomes, and their subsequent trafficking to lysosomes relies on the activity of small RAB GTPases, which are essential factors of cellular vesicle transport systems. The activity of RAB GTPases is coordinated by upstream factors, which include guanine nucleotide exchange factors (RAB GEFs) and RAB GTPase activating proteins (RAB GAPs). A role in macroautophagy regulation for different TRE2-BUB2-CDC16 (TBC) domain-containing RAB GAPs has been established. Recently, however, a positive modulation of macroautophagy has also been demonstrated for the TBC domain-free RAB3GAP1/2, adding to the family of RAB GAPs that coordinate macroautophagy and additional cellular trafficking pathways.
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250241/European Research Council
Animals
Autophagy
GTPase-Activating Proteins
Guanine Nucleotide Exchange Factors
Humans
Lysosomes
Protein Transport
rab GTP-Binding Proteins
GTPase-Activating Proteins
Guanine Nucleotide Exchange Factors
rab GTP-Binding Proteins