Division of Molecular, Cellular, and Developmental Biology, University of Dundee, Dundee DD1 5EH, United Kingdom.
Centre for Regenerative Medicine, Institute for Regeneration and Repair, Institute for Stem Cell Research, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Genes Dev. 2024 Nov 27;38(21-24):952-964. doi: 10.1101/gad.352176.124.
The link between DNA methylation and neurodevelopmental disorders is well established. However, how DNA methylation is fine-tuned-ensuring precise gene expression and developmental fidelity-remains poorly understood. PROSER1, a known TET2 interactor, was recently linked to a severe neurodevelopmental disorder. Here, we demonstrate that PROSER1 interacts with all TET enzymes and stabilizes chromatin-bound TET-OGT-PROSER1-DBHS (TOPD) complexes, which regulate DNA demethylation and developmental gene expression. Surprisingly, we found that PROSER1 also sequesters TET enzymes, preventing widespread demethylation and transposable element derepression. Our findings identify PROSER1 as a key factor that both positively and negatively regulates DNA demethylation essential for mammalian neurodevelopment.
DNA 甲基化与神经发育障碍之间的联系已得到充分证实。然而,DNA 甲基化如何被精细调控,以确保精确的基因表达和发育保真度,仍知之甚少。PROSER1 是一种已知的 TET2 相互作用蛋白,最近与一种严重的神经发育障碍有关。在这里,我们证明 PROSER1 与所有 TET 酶相互作用,并稳定结合在染色质上的 TET-OGT-PROSER1-DBHS(TOPD)复合物,该复合物调节 DNA 去甲基化和发育基因表达。令人惊讶的是,我们发现 PROSER1 还可以隔离 TET 酶,防止广泛的去甲基化和转座元件去抑制。我们的研究结果表明,PROSER1 是一个关键因素,它既能正向又能负向调节 DNA 去甲基化,这对哺乳动物的神经发育至关重要。