The State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, College of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Key Laboratory of Photobiology, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Cell Mol Life Sci. 2021 Jan;78(1):129-141. doi: 10.1007/s00018-020-03594-9. Epub 2020 Jul 8.
AlkB homologs (ALKBH) are a family of specific demethylases that depend on Fe and α-ketoglutarate to catalyze demethylation on different substrates, including ssDNA, dsDNA, mRNA, tRNA, and proteins. Previous studies have made great progress in determining the sequence, structure, and molecular mechanism of the ALKBH family. Here, we first review the multi-substrate selectivity of the ALKBH demethylase family from the perspective of sequence and structural evolution. The construction of the phylogenetic tree and the comparison of key loops and non-homologous domains indicate that the paralogs with close evolutionary relationship have similar domain compositions. The structures show that the lack and variations of four key loops change the shape of clefts to cause the differences in substrate affinity, and non-homologous domains may be related to the compatibility of multiple substrates. We anticipate that the new insights into selectivity determinants of the ALKBH family are useful for understanding the demethylation mechanisms.
ALKB 同系物 (ALKBH) 是一类特异性去甲基酶,依赖于 Fe 和 α-酮戊二酸来催化不同底物的去甲基化,包括 ssDNA、dsDNA、mRNA、tRNA 和蛋白质。先前的研究在确定 ALKBH 家族的序列、结构和分子机制方面取得了很大进展。在这里,我们首先从序列和结构演化的角度回顾了 ALKBH 去甲基酶家族的多底物选择性。系统发生树的构建和关键环和非同源结构域的比较表明,进化关系密切的旁系同源物具有相似的结构域组成。结构表明,四个关键环的缺失和变化改变了裂隙的形状,导致底物亲和力的差异,而非同源结构域可能与多种底物的兼容性有关。我们预计,对 ALKBH 家族选择性决定因素的新认识将有助于理解去甲基化机制。