TDP-43 suppresses tau expression via promoting its mRNA instability

Jianlan Gu(Nantong University), Feng Wu(Nantong University), Wen Xu(Nantong University), Jianhua Shi(Nantong University), Wen Hu(Nantong University), Nana Jin(Nantong University), Wei Qian(Nantong University), Xinglong Wang(Case Western Reserve University), Khalid Iqbal(New York State Office for People With Developmental Disabilities), Cheng-Xin Gong(Nantong University), Fei Liu(Nantong University)
Nucleic Acids Research
March 6, 2017
Cited by 76Open Access
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Abstract

In the brains of individuals with Alzheimer's disease (AD) and chronic traumatic encephalopathy, tau pathology is accompanied usually by intracellular aggregation of transactive response DNA-binding protein 43 (TDP-43). However, the role of TDP-43 in tau pathogenesis is not understood. Here, we investigated the role of TDP-43 in tau expression in vitro and in vivo. We found that TDP-43 suppressed tau expression by promoting its mRNA instability through the UG repeats of its 3΄-untranslated region (3΄-UTR). The C-terminal region of TDP-43 was required for this function. Neurodegenerative diseases-causing TDP-43 mutations affected tau mRNA instability differentially, in that some promoted and others did not significantly affect tau mRNA instability. The expression levels of tau and TDP-43 were inverse in the frontal cortex and the cerebellum. Accompanied with cytoplasmic accumulation of TDP-43, tau expression was elevated in TDP-43M337V transgenic mouse brains. The level of TDP-43, which is decreased in AD brains, was found to correlate negatively with the tau level in human brain. Our findings indicate that TDP-43 suppresses tau expression by promoting the instability of its mRNA. Down-regulation of TDP-43 may be involved in the tau pathology in AD and related neurodegenerative disorders.


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