4.8 Editorial Material

VCP/p97 modulates PtdIns3P production and autophagy initiation

期刊

AUTOPHAGY
卷 17, 期 4, 页码 1052-1053

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/15548627.2021.1898742

关键词

ATXN3; autophagy initiation; beclin 1; PI(3)P; PI3K; VCP; p97

资金

  1. AstraZeneca
  2. European Molecular Biology Organization [ALTF 1024-2016, ALTF 135-2016]
  3. Alzheimer's Research UK
  4. Tau Consortium
  5. UK Dementia Research Institute [UKDRI-2002]
  6. Swedish Natural Research Council [2016-06605]
  7. Swedish Research Council [2016-06605] Funding Source: Swedish Research Council

向作者/读者索取更多资源

VCP protein plays a role in promoting autophagosome biogenesis by regulating the levels of PtdIns3P, stabilizing autophagy-related proteins through interactions with ATXN3 and the PtdIns3K complex.
VCP/p97 is an essential multifunctional protein implicated in a plethora of intracellular quality control systems, and abnormal function of VCP is the underlying cause of several neurodegenerative disorders. We reported that VCP regulates the levels of the macroautophagy/autophagy-inducing lipid phosphatidylinositol-3-phosphate (PtdIns3P) by modulating the activity of the BECN1 (beclin 1)-containing phosphatidylinositol 3-kinase (PtdIns3K) complex. VCP stimulates the deubiquitinase activity of ATXN3 (ataxin 3) to stabilize BECN1 protein levels and also interacts with and promotes the assembly and kinase activity of the PtdIns3K complex. Acute inhibition of VCP activity impairs autophagy induction, demonstrated by a diminished PtdIns3P production and decreased recruitment of early autophagy markers WIPI2 and ATG16L1. Thus, VCP promotes autophagosome biogenesis, in addition to its previously described role in autophagosome maturation.

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