K235 acetylation couples with PSPC1 to regulate the m6A demethylation activity of ALKBH5 and tumorigenesis
Xiaolan Zhang, Xinhui Chen, Binwu Xu, Min Chen, Song Zhu, Nan Meng, Jizhong Wang, Hui‐Fang Zhu, De Chen, Jinbao Liu, Guang‐Rong Yan
Abstract
Abstract N6-methyladenosine (m 6 A) modification plays important roles in bioprocesses and diseases. AlkB homolog 5 (ALKBH5) is one of two m 6 A demethylases. Here, we reveal that ALKBH5 is acetylated at lysine 235 (K235) by lysine acetyltransferase 8 and deacetylated by histone deacetylase 7. K235 acetylation strengthens the m 6 A demethylation activity of ALKBH5 by increasing its recognition of m 6 A on mRNA. RNA-binding protein paraspeckle component 1 (PSCP1) is a regulatory subunit of ALKBH5 and preferentially interacts with K235-acetylated ALKBH5 to recruit and facilitate the recognition of m 6 A mRNA by ALKBH5, thereby promoting m 6 A erasure. Mitogenic signals promote ALKBH5 K235 acetylation. K235 acetylation of ALKBH5 is upregulated in cancers and promotes tumorigenesis. Thus, our findings reveal that the m 6 A demethylation activity of ALKBH5 is orchestrated by its K235 acetylation and regulatory subunit PSPC1 and that K235 acetylation is necessary for the m 6 A demethylase activity and oncogenic roles of ALKBH5.