NEDDylation promotes nuclear protein aggregation and protects the Ubiquitin Proteasome System upon proteotoxic stress.
NEDDylation promotes nuclear protein aggregation and protects the Ubiquitin Proteasome System upon proteotoxic stress.
复制标题
DOI:
10.1038/s41467-018-06365-0
复制
发表时间:
2018-10-22
影响因子:
16.6
通讯作者:
Xirodimas DP
中科院分区:
文献类型:
--
作者:
Maghames CM;Lobato-Gil S;Perrin A;Trauchessec H;Rodriguez MS;Urbach S;Marin P;Xirodimas DP
Spatial management of stress-induced protein aggregation is an integral part of the proteostasis network. Protein modification by the ubiquitin-like molecule NEDD8 increases upon proteotoxic stress and it is characterised by the formation of hybrid NEDD8/ubiquitin conjugates. However, the biological significance of this response is unclear. Combination of quantitative proteomics with biological analysis shows that, during proteotoxic stress, NEDDylation promotes nuclear protein aggregation, including ribosomal proteins as a major group. This correlates with protection of the nuclear Ubiquitin Proteasome System from stress-induced dysfunction. Correspondingly, we show that NEDD8 compromises ubiquitination and prevents targeting and processing of substrates by the proteasome. Moreover, we identify HUWE1 as a key E3-ligase that is specifically required for NEDDylation during proteotoxic stress. The study reveals a specific role for NEDD8 in nuclear protein aggregation upon stress and is consistent with the concept that transient aggregate formation is part of a defence mechanism against proteotoxicity. Protein NEDDylation increases upon proteotoxic stress but the function of this response remains to be elucidated. Here, the authors show that NEDDylation contributes to the cellular defence against proteotoxicity by promoting nuclear protein aggregation and protecting the ubiquitin proteasome system.
登录
查看更多内容
影响因子:
4.7
作者:
de Oliveira GA;Rangel LP;Costa DC;Silva JL
通讯作者:
Silva JL
DOI:
10.1083/jcb.143.7.1883
发表时间:
1998-12-28
期刊:
The Journal of cell biology
影响因子:
--
作者:
Johnston JA;Ward CL;Kopito RR
通讯作者:
Kopito RR
影响因子:
9.8
作者:
David DC;Ollikainen N;Trinidad JC;Cary MP;Burlingame AL;Kenyon C
通讯作者:
Kenyon C
影响因子:
8.6
作者:
Chojnacki M;Mansour W;Hameed DS;Singh RK;El Oualid F;Rosenzweig R;Nakasone MA;Yu Z;Glaser F;Kay LE;Fushman D;Ovaa H;Glickman MH
通讯作者:
Glickman MH
影响因子:
7.2
作者:
Chen, Bryan;Retzlaff, Marco;Frydman, Judith
通讯作者:
Frydman, Judith