Stress modulates Ahi1-dependent nuclear localization of ten-eleven translocation protein 2. Issue 22 (3rd July 2021)

• Record Type: Journal Article
• Authors: Zhang, Qian; Hu, Qicheng; Wang, Junjie; Miao, Zhigang; Li, Ziyi; Zhao, Yuwen; Wan, Bo; Allen, Emily G; Sun, Miao; Jin, Peng; Xu, Xingshun
• Is Part Of: Human molecular genetics. Volume 30:Issue 22(2021)
• Page Start: 2149
• Page End: 2160
• Publication Date: 2021-07-03
• Subjects: Human molecular genetics -- Periodicals; Human chromosome abnormalities -- Periodicals; 572.8
• DOI: 10.1093/hmg/ddab179
• Languages: English
• ISSNs: 0964-6906

Abstract

Abstract: Major depression disorder is one of the most common psychiatric diseases. Recent evidence supports that environmental stress affects gene expression and promotes the pathological process of depression through epigenetic mechanisms. Three ten-eleven translocation (Tet) enzymes are epigenetic regulators of gene expression that promote 5-hydroxymethylcytosine (5hmC) modification of genes. Here, we show that the loss of Tet2 can induce depression-like phenotypes in mice. Paradoxically, using the paradigms of chronic stress, such as chronic mild stress and chronic social defeat stress, we found that depressive behaviors were associated with increased Tet2 expression but decreased global 5hmC level in hippocampus. We examined the genome-wide 5hmC profile in the hippocampus of Tet2 knockout mice and identified 651 dynamically hydroxymethylated regions, some of which overlapped with known depression-associated loci. We further showed that chronic stress could induce the abnormal nuclear translocation of Tet2 protein from cytosol. Through Tet2 immunoprecipitation and mass spectrum analyses, we identified a cellular trafficking protein, Abelson helper integration site-1 (Ahi1), which could interact with Tet2 protein. Ahi1 knockout or knockdown caused the accumulation of Tet2 in cytosol. The reduction of Ahi1 protein under chronic stress explained the abnormal Ahi1-dependent nuclear translocation of Tet2. These findings together provide the evidence for a critical role of modulating Tet2 nuclear translocation in regulating stress response.