Zinc and Its Transporters in Epigenetics

被引:36
作者
Brito, Sofia [1 ]
Lee, Mi-Gi [2 ]
Bin, Bum-Ho [1 ]
Lee, Jong-Soo [1 ]
机构
[1] Ajou Univ, Dept Biol Sci, Suwon 16499, South Korea
[2] Gyeonggido Business & Sci Accelerator, Bioctr, Suwon 16229, South Korea
基金
新加坡国家研究基金会;
关键词
epigenetics; zinc; zinc transporter; DE-NOVO METHYLATION; DNA METHYLATION; HISTONE ACETYLTRANSFERASES; CRYSTAL-STRUCTURE; CATALYTIC DOMAIN; PROTEIN; METALLOTHIONEIN; ACETYLATION; BINDING; FAMILY;
D O I
10.14348/molcells.2020.0026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epigenetic events like DNA methylation and histone modification can alter heritable phenotypes. Zinc is required for the activity of various epigenetic enzymes, such as DNA methyltransferases (DNMTs), histone acetyltransferases (HATs), histone deacetylases (HDACs), and histone demethylases, which possess several zinc binding sites. Thus, the dysregulation of zinc homeostasis can lead to epigenetic alterations. Zinc homeostasis is regulated by Zinc Transporters (ZnTs), Zrt(-) and Irt-like proteins (ZIPs), and the zinc storage protein metallothionein (MT). Recent advances revealed that ZIPs modulate epigenetics. ZIP10 deficiency was found to result in reduced HATs, confirming its involvement in histone acetylation for rigid skin barrier formation. ZIP13 deficiency, which is associated with Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS), increases DNMT activity, leading to dysgenesis of dermis via improper gene expressions. However, the precise molecular mechanisms remain to be elucidated. Future molecular studies investigating the involvement of zinc and its transporters in epigenetics are warranted.
引用
收藏
页码:323 / 330
页数:8
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