SMURF1 mediates damaged lysosomal homeostasis by ubiquitinating PPP3CB to promote the activation of TFEB.

Qin Xia, Xuan Liu, Lu Zhong, Jun Qu, Lei Dong
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Abstract

The calcium-activated phosphatase PPP3/calcineurin dephosphorylates TFEB (transcription factor EB) to trigger its nuclear translocation and the activation of macroautophagic/autophagic targets. However, the detailed molecular mechanism regulating TFEB activation remains poorly understood. Here, we highlighted the importance of SMURF1 (SMAD specific E3 ubiquitin protein ligase 1) in the activation of TFEB for lysosomal homeostasis. SMURF1 deficiency prevents the calcium-triggered ubiquitination of the catalytic subunit of PPP3/calcineurin in a manner consistent with defective autophagic degradation of damaged lysosomes. Mechanically, PPP3CB/CNA2 plays a bridging role in the recruitment of SMURF1 by LGALS3 (galectin 3) upon lysosome damage. Importantly, PPP3CB increases the dissociation of the N-terminal tail (NT) and C-terminal carbohydrate-recognition domain (CRD) of LGALS3, which may promote the formation of open conformers in a PPP3CB dephosphorylation activity-dependent manner. In addition, PPP3CB is ubiquitinated at lysine 146 by the recruited SMURF1 in response to intracellular calcium stimulation. The K63-linked ubiquitination of PPP3CB enhances the recruitment of TFEB. Moreover, TFEB directly interacts with both PPP3CB and the regulatory subunit PPP3R1 which facilitate the conformational correction of TFEB for its activation for the transcription of TFEB-targeted genes. Altogether, our results highlighted a critical mechanism for the regulation of PPP3/calcineurin activity via its ubiquitin ligase SMURF1 in response to lysosomal membrane damage, which may account for a potential target for the treatment of stress-related diseases.Abbreviation AID: autoinhibitory domain; ATG: autophagy related; CD: catalytic domain; CRD: carbohydrate-recognition domain; CsA: cyclosporin A; DMSO: dimethyl sulfoxide; ESCRT: endosomal sorting complexes required for transport; GSK3B: glycogen synthase kinase 3 beta; LAMP1: lysosomal associated membrane protein 1; LGALS3: galectin 3; LLOMe: L-leucyl-L-leucine methyl ester; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; ML-SA1: mucolipin synthetic agonist 1; MTORC1: mechanistic target of rapamycin kinase complex 1; NT: N-terminal tail; PPP3CB: protein phosphatase 3 catalytic subunit beta; PPP3R1: protein phosphatase 3 regulatory subunit B, alpha; SMURF1: SMAD specific E3 ubiquitin protein ligase 1; SQSTM1/p62: sequestosome 1; TFEB: transcription factor EB; VCP/p97: valosin containing protein; YWHA/14-3-3: tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein.

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SMURF1 通过泛素化 PPP3CB 来促进 TFEB 的活化,从而介导受损溶酶体的稳态。
钙激活磷酸酶 PPP3/calcineurin 可使 TFEB(转录因子 EB)去磷酸化,从而引发其核转位并激活大自噬/自噬靶标。然而,调控 TFEB 激活的详细分子机制仍鲜为人知。在这里,我们强调了SMURF1(SMAD特异性E3泛素蛋白连接酶1)在激活TFEB促进溶酶体稳态中的重要性。SMURF1 缺乏会阻止钙触发的 PPP3/calcineurin 催化亚基泛素化,其方式与受损溶酶体的自噬降解缺陷一致。从机理上讲,PPP3CB/CNA2 在溶酶体损伤后 LGALS3(galectin 3)招募 SMURF1 的过程中起着桥接作用。重要的是,PPP3CB 增加了 LGALS3 的 N 端尾(NT)和 C 端碳水化合物识别域(CRD)的解离,这可能会以 PPP3CB 去磷酸化活性依赖的方式促进开放构象的形成。此外,PPP3CB 在赖氨酸 146 处被招募的 SMURF1 泛素化,以响应细胞内的钙刺激。PPP3CB 的 K63 链接泛素化增强了 TFEB 的招募。此外,TFEB 直接与 PPP3CB 和调控亚基 PPP3R1 相互作用,从而促进 TFEB 的构象校正,以激活 TFEB 靶向基因的转录。总之,我们的研究结果突显了溶酶体膜损伤时通过泛素连接酶 SMURF1 调节 PPP3/calcineurin 活性的关键机制,这可能是治疗应激相关疾病的潜在靶点。
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