RNF2 is recruited by WASH to ubiquitinate AMBRA1 leading to downregulation of autophagy

被引:81
|
作者
Xia, Pengyan [1 ,2 ]
Wang, Shuo [1 ]
Huang, Guanling [1 ,2 ]
Du, Ying [1 ]
Zhu, Pingping [1 ]
Li, Man [1 ,2 ]
Fan, Zusen [1 ]
机构
[1] Chinese Acad Sci, Inst Biophys, Key Lab Infect & Immun CAS, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
WASH; RNF2; AMBRA1; polyubiquitination; the BECN1-PIK3C3 complex; INHIBITS AUTOPHAGY; HISTONE H2A; PROTEINS; COMPLEX; LIGASE; UBIQUITYLATION; BECLIN-1; UVRAG; SUPPRESSION; BIOGENESIS;
D O I
10.1038/cr.2014.85
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
WASH (Wiskott-Aldrich syndrome protein (WASP) and SCAR homolog) was identified to function in endosomal sorting via Arp2/3 activation. We previously demonstrated that WASH is a new interactor of BECN1 and present in the BECN1-PIK3C3 complex with AMBRA1. The AMBRA1-DDB1-CUL4A complex is an E3 ligase for K63-linked ubiquitination of BECN1, which is required for starvation-induced autophagy. WASH suppresses autophagy by inhibition of BECN1 ubiquitination. However, how AMBRA1 is regulated during autophagy remains elusive. Here, we found that RNF2 associates with AMBRA1 to act as an E3 ligase to ubiquitinate AMBRA1 via K48 linkage. RNF2 mediates ubiquitination of AMBRA1 at lysine 45. Notably, RNF2 deficiency enhances autophagy induction. Upon autophagy induction, RNF2 potentiates AMBRA1 degradation with the help of WASH. WASH deficiency impairs the association of RNF2 with AMBRA1 to impede AMBRA1 degradation. Our findings reveal another novel layer of regulation of autophagy through WASH recruitment of RNF2 for AMBRA1 degradation leading to downregulation of autophagy.
引用
收藏
页码:943 / 958
页数:16
相关论文
共 50 条
  • [21] The autophagy regulators Ambra1 and Beclin 1 are required for adult neurogenesis in the brain subventricular zone
    Yazdankhah, M.
    Farioli-Vecchioli, S.
    Tonchev, A. B.
    Stoykova, A.
    Cecconi, F.
    CELL DEATH & DISEASE, 2014, 5 : e1403 - e1403
  • [22] Repression of the Autophagy Gene AMBRA1 in the Developing Neuroepithelium Is a Novel Mechanism Underlying Diabetic Embryopathy
    Chen, X.
    BIRTH DEFECTS RESEARCH, 2018, 110 (09): : 761 - 761
  • [23] RhoBTB3 Functions as a Novel Regulator of Autophagy by Suppressing AMBRA1 Stability
    Kim, Kyungho
    Kim, Dong-Gun
    Kim, Youn-Jae
    CELLS, 2024, 13 (19)
  • [24] The autophagy protein Ambra1 regulates gene expression by supporting novel transcriptional complexes
    Schoenherr, Christina
    Byron, Adam
    Griffith, Billie
    Loftus, Alexander
    Wills, Jimi C.
    Munro, Alison F.
    von Kriegsheim, Alex
    Frame, Margaret C.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2020, 295 (34) : 12045 - 12057
  • [25] Unleashing the Ambra1-Beclin 1 complex from dynein chains Ulk1 sets Ambra1 free to induce autophagy
    Fimia, Gian Maria
    Di Bartolomeo, Sabrina
    Piacentini, Mauro
    Cecconi, Francesco
    AUTOPHAGY, 2011, 7 (01) : 115 - 117
  • [26] AMBRA1 Interplay with Cullin E3 Ubiquitin Ligases Regulates Autophagy Dynamics
    Antonioli, Manuela
    Albiero, Federica
    Nazio, Francesca
    Vescovo, Tiziana
    Perdomo, Ariel Basulto
    Corazzari, Marco
    Marsella, Claudia
    Piselli, Pierluca
    Gretzmeier, Christine
    Dengjel, Joern
    Cecconi, Francesco
    Piacentini, Mauro
    Fimia, Gian Maria
    DEVELOPMENTAL CELL, 2014, 31 (06) : 734 - 746
  • [27] Ambra1 modulates starvation-induced autophagy through AMPK signaling pathway in cardiomyocytes
    Shi, Conghong
    Wu, Jing
    Fu, Min
    Zhang, Baohong
    Wang, Juan
    Yang, Xi
    Chi, Yunpeng
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2014, 452 (03) : 308 - 314
  • [28] Melanoma secretion of TGFβ2 mediates epidermal AMBRA1 and Claudin1 downregulation, loss of epidermal integrity and tumour ulceration
    Cosgarea, I.
    Mc Connell, A.
    Tang, D.
    Greenwood, A.
    Ellis, R.
    Lovat, P.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2019, 139 (09) : S299 - S299
  • [29] Mutations in AMBRA1 aggravate β-thalassemia by impairing autophagy-mediated clearance of free α-globin
    Long, Yong
    Zhang, Qianqian
    Ling, Ling
    Zhuang, Yuan
    Wei, Xiaolei
    Huang, Haoyang
    Lu, Zhanping
    Huang, Yushan
    Chen, Xianming
    Ye, Yuhua
    Feng, Xiaoqin
    Zhang, Haokun
    Huang, Binbin
    Huang, Yueyan
    Liang, Yidan
    Fang, Mingyan
    Nakamura, Yukio
    Lin, Bin
    Zhang, Xinhua
    Lu, Daru
    Jin, Xin
    Xu, Xiangmin
    BLOOD, 2025, 145 (10) : 1074 - 1088
  • [30] A PRC1–RNF2 knockout punch for cancer
    Janneke G. C. Peeters
    Michel DuPage
    Nature Cancer, 2021, 2 : 996 - 997