Mitochondrial deoxyguanosine kinase (DGUOK) regulates NAD+ biogenesis independent of mitochondria complex I activity

Mitochondrial deoxyguanosine kinase (DGUOK) regulates NAD+ biogenesis independent of mitochondria complex I activity
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线粒体脱氧鸟苷激酶 (DGUOK) 独立于线粒体复合物 I 活性调节 NAD 生物合成

DOI:
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发表时间:
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影响因子:
4.7
通讯作者:
Jianwei Sun
Jianwei Sun
中科院分区:
医学3区
文献类型:
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作者:
Lei Sang;Ying-jie He;Jiaxin Kang;Hongyi Ye;Weiyu Bai;Xiao-dong Luo;Jianwei Sun

文献摘要

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Overexpression of DGUOK promotes mitochondria oxidative phosphorylation and lung adenocarcinoma progression. However, the role and mechanism of DGUOK in regulation of mitochondria function and lung cancer progression still poorly understood. Here we demonstrated that DGUOK regulated NAD+ biogenesis. Depletion of the DGUOK significantly decreased NAD+ level. Furthermore, knockout of the DGUOK considerably reduced expression of the NMNAT2, a key molecule controlling NAD+ synthesis, at both mRNA and protein levels. Ectopic expression of the NMNAT2 abrogated the effect of knockdown of DGUOK on NAD+. Notably, this regulation is independent of DGUOK -mediated mitochondria complex I activity. We also showed that NMNAT2 was highly expressed in lung adenocarcinoma and negatively correlated with the patient overall survival. Our study suggested that DGUOK regulates NAD+ in a NMNAT2 dependent manner and DGUOK-NMNAT2-NAD+ axis could be a potential therapeutic target in lung adenocarcinoma.