Abstract: Previous studies have indicated important roles for NIMA-related kinase 1 (NEK1) in modulating DNA damage checkpoints and DNA repair capacity. To broadly assess the contributions of NEK1 to genotoxic stress and mitochondrial functions, we characterised several relevant phenotypes of NEK1 CRISPR knockout (KO) and wild-type (WT) HAP1 cells. Our studies revealed that NEK1 KO cells resulted in increased apoptosis and hypersensitivity to the alkylator methyl methanesulfonate, the radiomimetic bleomycin and UVC light, yet increased resistance to the crosslinker cisplatin. Mitochondrial functionalities were also altered in NEK1 KO cells, with phenotypes of reduced mitophagy, increased total mitochondria, elevated levels of reactive oxygen species, impaired complex I activity and higher amounts of mitochondrial DNA damage. RNA-seq transcriptome analysis coupled with quantitative real-time PCR studies comparing NEK1 KO cells with NEK1 overexpressing cells revealed that the expression of genes involved in DNA repair pathways, such as base excision repair, nucleotide excision repair and double-strand break repair, are altered in a way that might influence genotoxin resistance. Together, our studies underline and further support that NEK1 serves as a hub signalling kinase in response to DNA damage, modulating DNA repair capacity, mitochondrial activity and cell fate determination. ; Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2016/02040-8, 2017/21067-7, 2017/03489-1, 2014/15982-6]; Coordenacao de Aperfeicoamento do Pessoal de Ensino Superior (CAPES) (Brasiia, DF,Brazil) Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [01]; Conselho Nacional de Pesquisa e Desenvolvimento (CNPq) (Brasiia, DF, Brazil)Conselho Nacional de Desenvolvimento Cientifico e (FAPDF) [308868/2018-8, 302534/2017-2]; Intramural Research Program of Tecnologico (CNPQ)Fundacao de Apoio a Pesquisa do Distrito Federal; the National Institute on Aging, National Institutes of Health United States Department of Health & ...
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