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Class III phosphatidylinositol 3-kinase complex I subunit NRBF2/Atg38-from cell and structural biology to health and disease

期刊

AUTOPHAGY
卷 17, 期 12, 页码 3897-3907

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/15548627.2021.1872240

关键词

atg38; membranes; nrbf2; pik3c3; ptdins3p; vps34

资金

  1. Medical Research Council [MC_U105184308]
  2. MRC [MC_U105184308] Funding Source: UKRI

向作者/读者索取更多资源

Macroautophagy/autophagy is triggered by various starvation and stress conditions, and essential for autophagosome formation is the phospholipid phosphatidylinositol-3-phosphate. The PIK3C3/Vps34 complex I, which includes NRBF2/Atg38 as a fifth component, plays a crucial role in autophagy initiation. With the field expanding, different conclusions have been drawn in various topics, highlighting the need for further clarification in the future.
Macroautophagy/autophagy is triggered by various starvation and stress conditions. The phospholipid phosphatidylinositol-3-phosphate (PtdIns3P) is essential for the formation of the autophagosome both in yeast and mammals. The class III phosphatidylinositol 3-kinase, PIK3C3C in humans or Vps34 in yeast, produces PtdIns3P by phosphorylating the 3MODIFIER LETTER PRIME-OH position of phosphatidylinositol (PtdIns). In order to synthesize PtdIns3P for the initiation of autophagy, PIK3C3/Vps34 has a heterotetrameric core, the PIK3C3 complex I (hereafter complex I) composed of PIK3C3/Vps34, PIK3R4/Vps15, BECN1/Vps30, and ATG14/Atg14. A fifth component of complex I, NRBF2 in mammals and Atg38 in yeast, was found and has been characterized in the past decade. The field has been expanding from cell and structural biology to mouse model and cohort studies. Here I will summarize the structures and models of complex I binding NRBF2/Atg38, its intracellular roles, and its involvement in health and disease. Along with this expansion of the field, different conclusions have been drawn in several topics. I will clarify what has and has not been agreed, and what is to be clarified in the future.

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