Trs20, Trs23, Trs31 and Bet5 participate in autophagy through GTPase Ypt1 in Saccharomyces cerevisiae

Authors

  • Shenshen Zou College of Life Sciences, Key Laboratory of Agricultural Environmental Microbiology of Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095
  • Yan Liu College of Life Sciences, Key Laboratory of Agricultural Environmental Microbiology of Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095
  • Gaoyi Min College of Life Sciences, Key Laboratory of Agricultural Environmental Microbiology of Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095
  • Yongheng Liang College of Life Sciences, Key Laboratory of Agricultural Environmental Microbiology of Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095

Keywords:

autophagy, TRAPP, common TRAPP subunits, Ypt1, Ypt31

Abstract

TRAPP (transport protein particle) is a large, highly conserved, multi-subunit complex. Four types of TRAPP complexes (I, II, III and most recently IV) have been identified in Saccharomyces cerevisiae. Studies on the roles of TRAPP II, TRAPP III and TRAPP IV specific subunits (Trs130, Trs85 and Trs33) have demonstrated that TRAPP II, TRAPP III and TRAPP IV activate the small GTPases that regulate autophagy. Up to now, the roles of the common TRAPP subunits have been well studied in vesicle transport. However, the roles of the common TRAPP subunits and their relationship to Ypt/Rab GTPases in autophagy are not clear. In this paper, we examined Trs20, Trs23, Trs31, and Bet5 (the common TRAPP subunits), which are required for starvation-induced autophagy and the cytoplasm-to-vacuole targeting (Cvt) pathway. During autophagy, GFP-Atg8 accumulates as single or multiple dots and is not recruited into the pre-autophagosomal structures (PAS) in trs20ts, trs23ts, trs31ts and bet5ts mutant cells. Furthermore, these dots are linked to the endoplasmic reticulum in mutant cells. Additionally, overexpression of Ypt1, but not Ypt31, suppresses the autophagy defect in trs20ts, trs23ts, trs31ts and bet5ts mutant cells. Based on these results, we concluded that Trs20, Trs23, Trs31, and Bet5 are required for autophagy, and that these common TRAPP subunits regulate autophagy partially through GTPase Ypt1, but not Ypt31.

https://doi.org/10.2298/ABS170408030Z

Received: April 8, 2017; Revised: June 20, 2017; Accepted: July 29, 2017; Published online: August 28, 2017

How to cite this article: Zou S, Liu Y, Min G, Liang Y. Trs20, Trs23, Trs31 and Bet5 participate in autophagy through GTPase Ypt1 in Saccharomyces cerevisiae. Arch Biol Sci. 2018;70(1):109-18.

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Published

2018-03-13

How to Cite

1.
Zou S, Liu Y, Min G, Liang Y. Trs20, Trs23, Trs31 and Bet5 participate in autophagy through GTPase Ypt1 in Saccharomyces cerevisiae. Arch Biol Sci [Internet]. 2018Mar.13 [cited 2024Dec.22];70(1):109-18. Available from: https://serbiosoc.org.rs/arch/index.php/abs/article/view/1663

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