Late endosomal microautophagy (Homo sapiens)

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84, 6, 722cytosollate endosome lumenUBC(1-76) UBC(457-532) misfolded CFTR HDAC6 UBB(153-228) UBC(381-456) RPS27A(1-76) UBC(229-304) UBB(1-76) PL UBB(153-228) UBC(609-684) HSPA8VPS28 Substrates forchaperone mediatedautophagyUBB(1-76) HDAC6 CHMP6 UBC(77-152) UBB(1-76) UBB(77-152) UBC(1-76) UBC(381-456) UBC(305-380) CHMP2B UBC(153-228) PolyUb-Misfolded cilia proteins UBB(153-228) PL:HSPA8:AutophagysubstrateUBC(533-608) Poly-vimentin UBC(229-304) CHMP4A VPS37B RNASE1 UBC(457-532) UBC(305-380) UBC(533-608) HDAC6 UBB(1-76) PolyUb-Misfolded PARK7 UBC(609-684) misfolded CFTR TSG101 UBC(77-152) HSPA8 Poly-vimentin UBC(533-608) CHMP4B Phosphorylated PLINs from lipid droplet surface UBC(77-152) PolyUb-Misfolded PARK7 PL:HSPA8:AutophagysubstrateVPS37A UBC(305-380) CHMP7 CHMP3 Phosphorylated PLINs from lipid droplet surface Poly-vimentin UBC(1-76) misfolded CFTR HBB UBB(77-152) UBA52(1-76) UBC(229-304) CHMP4C UBB(77-152) Phosphorylated PLINs from lipid droplet surface UBC(533-608) RNASE1 RNASE1 HSPA8 UBC(609-684) Poly-vimentin ESCRT-IHBB UBC(229-304) HBB UBB(77-152) PolyUb-Misfolded cilia proteins UBC(153-228) UBC(153-228) UBC(153-228) PLUBC(457-532) UBC(381-456) Phosphorylated PLINs from lipid droplet surface RPS27A(1-76) UBA52(1-76) UBC(609-684) misfolded CFTR CHMP2A VPS37D UBA52(1-76) UBAP1 PolyUb-Misfolded PARK7 UBA52(1-76) UBC(381-456) MVB12 RPS27A(1-76) RNASE1 HSPA8 boundautophagicsubstratesUBB(153-228) ESCRT-IIIPL UBC(77-152) PolyUb-Misfolded PARK7 UBC(305-380) PolyUb-Misfolded cilia proteins HDAC6 UBC(1-76) PolyUb-Misfolded cilia proteins RPS27A(1-76) VPS37C UBC(457-532) HBB HSPA8 1, 3, 5, 9


Description

Microautophagy (MI) is a non-selective autophagic pathway that involves internalisation of cytosolic cargo through invaginations of the lysosomal membrane. MI can be induced by nitrogen starvation and complements other related self-eating processes such as Macroautophagy (MA) and Chaperone Mediated Autophagy (CMA). MI can degrade cell organelles and bulk cytosolic proteins directly via the lysosome and late endosome. MI can also target substrates with KFERQ motifs with the help of HSPA8 (Li W W et al. 2012). View original pathway at Reactome.

Comments

Reactome-Converter 
Pathway is converted from Reactome ID: 9615710
Reactome-version 
Reactome version: 74
Reactome Author 
Reactome Author: Varusai, Thawfeek

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Ontology Terms

 

Bibliography

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  1. Dice JF.; ''Peptide sequences that target cytosolic proteins for lysosomal proteolysis.''; PubMed Europe PMC Scholia
  2. Kaushik S, Cuervo AM.; ''Degradation of lipid droplet-associated proteins by chaperone-mediated autophagy facilitates lipolysis.''; PubMed Europe PMC Scholia
  3. Sahu R, Kaushik S, Clement CC, Cannizzo ES, Scharf B, Follenzi A, Potolicchio I, Nieves E, Cuervo AM, Santambrogio L.; ''Microautophagy of cytosolic proteins by late endosomes.''; PubMed Europe PMC Scholia
  4. Chiang HL, Terlecky SR, Plant CP, Dice JF.; ''A role for a 70-kilodalton heat shock protein in lysosomal degradation of intracellular proteins.''; PubMed Europe PMC Scholia
  5. de Souza RF, Aravind L.; ''UMA and MABP domains throw light on receptor endocytosis and selection of endosomal cargoes.''; PubMed Europe PMC Scholia
  6. Agromayor M, Soler N, Caballe A, Kueck T, Freund SM, Allen MD, Bycroft M, Perisic O, Ye Y, McDonald B, Scheel H, Hofmann K, Neil SJ, Martin-Serrano J, Williams RL.; ''The UBAP1 subunit of ESCRT-I interacts with ubiquitin via a SOUBA domain.''; PubMed Europe PMC Scholia
  7. Stefani F, Zhang L, Taylor S, Donovan J, Rollinson S, Doyotte A, Brownhill K, Bennion J, Pickering-Brown S, Woodman P.; ''UBAP1 is a component of an endosome-specific ESCRT-I complex that is essential for MVB sorting.''; PubMed Europe PMC Scholia
  8. Li WW, Li J, Bao JK.; ''Microautophagy: lesser-known self-eating.''; PubMed Europe PMC Scholia
  9. Morita E, Sandrin V, Alam SL, Eckert DM, Gygi SP, Sundquist WI.; ''Identification of human MVB12 proteins as ESCRT-I subunits that function in HIV budding.''; PubMed Europe PMC Scholia

History

CompareRevisionActionTimeUserComment
114704view16:18, 25 January 2021ReactomeTeamReactome version 75
113149view11:21, 2 November 2020ReactomeTeamReactome version 74
112787view17:44, 9 October 2020DeSlOntology Term : 'microautophagy pathway' added !
112742view16:14, 9 October 2020ReactomeTeamNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
CHMP2A ProteinO43633 (Uniprot-TrEMBL)
CHMP2B ProteinQ9UQN3 (Uniprot-TrEMBL)
CHMP3 ProteinQ9Y3E7 (Uniprot-TrEMBL)
CHMP4A ProteinQ9BY43 (Uniprot-TrEMBL)
CHMP4B ProteinQ9H444 (Uniprot-TrEMBL)
CHMP4C ProteinQ96CF2 (Uniprot-TrEMBL)
CHMP6 ProteinQ96FZ7 (Uniprot-TrEMBL)
CHMP7 ProteinQ8WUX9 (Uniprot-TrEMBL)
ESCRT-IIIComplexR-HSA-9631182 (Reactome)
ESCRT-IComplexR-HSA-184398 (Reactome)
HBB ProteinP68871 (Uniprot-TrEMBL)
HDAC6 ProteinQ9UBN7 (Uniprot-TrEMBL)
HSPA8 ProteinP11142 (Uniprot-TrEMBL)
HSPA8 bound

autophagic

substrates
ComplexR-HSA-9615717 (Reactome)
HSPA8ProteinP11142 (Uniprot-TrEMBL)
MVB12 R-HSA-8959998 (Reactome)
PL MetaboliteCHEBI:16247 (ChEBI)
PL:HSPA8:Autophagy substrateComplexR-HSA-9631070 (Reactome)
PL:HSPA8:Autophagy substrateComplexR-HSA-9631107 (Reactome)
PLMetaboliteCHEBI:16247 (ChEBI)
Phosphorylated PLINs from lipid droplet surface R-HSA-9613669 (Reactome)
Phosphorylated PLINs from lipid droplet surface R-HSA-9639399 (Reactome)
Poly-vimentin R-HSA-9646678 (Reactome)
Poly-vimentin R-HSA-9660015 (Reactome)
PolyUb-Misfolded PARK7 ProteinQ99497 (Uniprot-TrEMBL)
PolyUb-Misfolded cilia proteins R-HSA-9641108 (Reactome)
PolyUb-Misfolded cilia proteins R-HSA-9659976 (Reactome)
RNASE1 ProteinP07998 (Uniprot-TrEMBL)
RPS27A(1-76) ProteinP62979 (Uniprot-TrEMBL)
Substrates for

chaperone mediated

autophagy
ComplexR-HSA-9615715 (Reactome)
TSG101 ProteinQ99816 (Uniprot-TrEMBL)
UBA52(1-76) ProteinP62987 (Uniprot-TrEMBL)
UBAP1 ProteinQ9NZ09 (Uniprot-TrEMBL)
UBB(1-76) ProteinP0CG47 (Uniprot-TrEMBL)
UBB(153-228) ProteinP0CG47 (Uniprot-TrEMBL)
UBB(77-152) ProteinP0CG47 (Uniprot-TrEMBL)
UBC(1-76) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(153-228) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(229-304) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(305-380) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(381-456) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(457-532) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(533-608) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(609-684) ProteinP0CG48 (Uniprot-TrEMBL)
UBC(77-152) ProteinP0CG48 (Uniprot-TrEMBL)
VPS28 ProteinQ9UK41 (Uniprot-TrEMBL)
VPS37A ProteinQ8NEZ2 (Uniprot-TrEMBL)
VPS37B ProteinQ9H9H4 (Uniprot-TrEMBL)
VPS37C ProteinA5D8V6 (Uniprot-TrEMBL)
VPS37D ProteinQ86XT2 (Uniprot-TrEMBL)
misfolded CFTR ProteinP13569 (Uniprot-TrEMBL)

Annotated Interactions

View all...
SourceTargetTypeDatabase referenceComment
ESCRT-IArrowR-HSA-9631065 (Reactome)
ESCRT-IIIArrowR-HSA-9631065 (Reactome)
HSPA8 bound

autophagic

substrates
ArrowR-HSA-9615721 (Reactome)
HSPA8 bound

autophagic

substrates
R-HSA-9631068 (Reactome)
HSPA8R-HSA-9615721 (Reactome)
PL:HSPA8:Autophagy substrateArrowR-HSA-9631065 (Reactome)
PL:HSPA8:Autophagy substrateArrowR-HSA-9631068 (Reactome)
PL:HSPA8:Autophagy substrateR-HSA-9631065 (Reactome)
PLR-HSA-9631068 (Reactome)
R-HSA-9615721 (Reactome) Intracellular proteins are targeted for proteolytic degradation in the lysosome with the aid of chaperones. Heat shock cognate 71 kDa protein (HSPA8) acts as the constitutive chaperone that binds substrate proteins in the cytosol. HSPA8 recognizes a motif based on the charge of the amino acids (Chiang H et al. 1989, Dice JF et al. 1990). This allows the motif to have multiple sequence possibilities and also create a motif through post-translational modifications such as phosphorylation and acetylation. Once bound with HSPA8, the substrates are targeted to the lysosome or endosome.
R-HSA-9631065 (Reactome) In addition to bulk protein degradation, Microautophagy (MI) can also target KFERQ motif protein substrates similar to Chaperone Mediated Autophagy (CMA). However, MI is distinct from CMA in that it occurs during late endosomes/multivesicular bodies formation. Upon binding with Hspa8, substrates are transported from the cytosol to late endosomes. HSPA8 binds with the phospholipids on the late endosomal membrane. Subsequently, the substrate is transported into the lumen via endosomal sorting complexes required for transport (ESCRTI and ESCRTIII systems) (Sahu R et al. 2011). This event is represented as a black box since the precise molecular mechanism of the substrate transport into the endosomal lumen is unclear. Experiments confirming this event were performed in mouse.
R-HSA-9631068 (Reactome) Microautophagy (MI) can target KFERQ motif containing protein substrates to endosomal degradation. Upon binding with HSPA8, substrates are transported from the cytosol to late endosomes. Here, HSPA8 binds with the phospholipids on the late endosomal membrane. This interaction facilitates the vesicle-mediated transport of HSPA8:substrate complex into the late endosomes for degradation (Sahu R et al. 2011). Experiments confirming this interaction were performed in mouse cells.
Substrates for

chaperone mediated

autophagy
R-HSA-9615721 (Reactome)
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