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NEK10 interactome and depletion reveal new roles in mitochondria

Authors :
Camila de Castro Ferezin
Andressa Peres de Oliveira
Jörg Kobarg
Edmarcia Elisa de Souza
Carlos Frederico Martins Menck
Leonardo R. Silveira
Fernanda Luisa Basei
Valquiria Tiago dos Santos
Talita Diniz Melo-Hanchuk
Priscila Ferreira Slepicka
Davi Mendes
Tanes I. Lima
Source :
Proteome Science, Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual), Universidade de São Paulo (USP), instacron:USP, Proteome Science, Vol 18, Iss 1, Pp 1-17 (2020)
Publication Year :
2019

Abstract

BackgroundMembers of the family of NEK protein kinases (NIMA-related kinases) were described to have crucial roles in regulating different aspects of the cell cycle. NEK10 was reported to take part in the maintenance of the G2/M checkpoint after exposure to ultraviolet light. NEK1, NEK5, NEK2 and NEK4 proteins on the other hand have been linked to mitochondrial functions.MethodsHEK293T cells were transfected with FLAG empty vector or FLAG-NEK10 and treated or not with Zeocin. For proteomic analysis, proteins co-precipitated with the FLAG constructs were digested by trypsin, and then analyzed via LC-MS/MS. Proteomic data retrieved were next submitted to Integrated Interactome System analysis and differentially expressed proteins were attributed to Gene Ontology biological processes and assembled in protein networks by Cytoscape. For functional, cellular and molecular analyses two stable Nek10 silenced HeLa cell clones were established.ResultsHere, we discovered the following possible new NEK10 protein interactors, related to mitochondrial functions: SIRT3, ATAD3A, ATAD3B, and OAT. After zeocin treatment, the spectrum of mitochondrial interactors increased by the proteins: FKBP4, TXN, PFDN2, ATAD3B, MRPL12, ATP5J, DUT, YWHAE, CS, SIRT3, HSPA9, PDHB, GLUD1, DDX3X, and APEX1. We confirmed the interaction of NEK10 and GLUD1 by proximity ligation assay and confocal microscopy. Furthermore, we demonstrated that NEK10-depleted cells showed more fragmented mitochondria compared to the control cells. The knock down of NEK10 resulted further in changes in mitochondrial reactive oxygen species (ROS) levels, decreased citrate synthase activity, and culminated in inhibition of mitochondrial respiration, affecting particularly ATP-linked oxygen consumption rate and spare capacity. NEK10 depletion also decreased the ratio of mtDNA amplification, possibly due to DNA damage. However, the total mtDNA content increased, suggesting that NEK10 may be involved in the control of mtDNA content.ConclusionsTaken together these data place NEK10 as a novel regulatory player in mitochondrial homeostasis and energy metabolism.

Details

ISSN :
14775956
Volume :
18
Database :
OpenAIRE
Journal :
Proteome science
Accession number :
edsair.doi.dedup.....00a8bf4066bd6723e5fb182ec9c63c86