Switzer Rebecca L, Hartman Zach J, Hewett Geoffrey R, Carroll Clara F
Department of Chemistry, Bucknell University, Lewisburg, PA 17837, USA.
Department of Biology, Bucknell University, Lewisburg, PA 17837, USA.
DNA (Basel). 2023 Sep;3(3):119-133. doi: 10.3390/dna3030010. Epub 2023 Jul 13.
DNA methyltransferase 1 (DNMT1) is the enzyme primarily responsible for propagation of the methylation pattern in cells. Mutations in DNMT1 have been linked to the development of adult-onset neurodegenerative disorders; these disease-associated mutations occur in the regulatory replication foci-targeting sequence (RFTS) domain of the protein. The RFTS domain is an endogenous inhibitor of DNMT1 activity that binds to the active site and prevents DNA binding. Here, we examine the impact of the disease-associated mutation A554V on normal RFTS-mediated inhibition of DNMT1. Wild-type and mutant proteins were expressed and purified to homogeneity for biochemical characterization. The mutation increased DNA binding affinity ~8-fold. In addition, the mutant enzyme exhibited increased DNA methylation activity. Circular dichroism (CD) spectroscopy revealed that the mutation does not significantly impact the secondary structure or relative thermal stability of the isolated RFTS domain. However, the mutation resulted in changes in the CD spectrum in the context of the larger protein; a decrease in relative thermal stability was also observed. Collectively, this evidence suggests that A554V disrupts normal RFTS-mediated autoinhibition of DNMT1, resulting in a hyperactive mutant enzyme. While the disease-associated mutation does not significantly impact the isolated RFTS domain, the mutation results in a weakening of the interdomain stabilizing interactions generating a more open, active conformation of DNMT1. Hyperactive mutant DNMT1 could be responsible for the increased DNA methylation observed in affected individuals.
DNA甲基转移酶1(DNMT1)是主要负责在细胞中传播甲基化模式的酶。DNMT1中的突变与成年期神经退行性疾病的发生有关;这些与疾病相关的突变发生在该蛋白的调节性复制灶靶向序列(RFTS)结构域中。RFTS结构域是DNMT1活性的内源性抑制剂,它与活性位点结合并阻止DNA结合。在这里,我们研究了与疾病相关的突变A554V对正常RFTS介导的DNMT1抑制作用的影响。表达并纯化野生型和突变型蛋白至均一性以进行生化特性分析。该突变使DNA结合亲和力增加了约8倍。此外,突变酶表现出增加的DNA甲基化活性。圆二色性(CD)光谱显示,该突变对分离的RFTS结构域的二级结构或相对热稳定性没有显著影响。然而,在较大蛋白质的背景下,该突变导致CD光谱发生变化;还观察到相对热稳定性降低。总体而言,这些证据表明A554V破坏了正常RFTS介导的DNMT1自抑制作用,导致产生一种活性过高的突变酶。虽然与疾病相关的突变对分离的RFTS结构域没有显著影响,但该突变导致结构域间稳定相互作用减弱,从而产生一种更开放、活性更高的DNMT1构象。活性过高的突变型DNMT1可能是导致受影响个体中观察到的DNA甲基化增加的原因。