表观遗传学
脱甲基酶
铁转运蛋白
缺铁
生物
组蛋白
海西定
甲基转移酶
生物化学
甲基化
内科学
医学
基因
免疫学
炎症
贫血
作者
Bashar Farida,Kasimu Ghandi Ibrahim,Bilyaminu Abubakar,Ibrahim Malami,Muhammad Bashir Bello,Murtala Bello Abubakar,Abdullahi Y. Abbas,Mustapha Umar Imam
标识
DOI:10.1016/j.jtemb.2023.127203
摘要
Iron deficiency is a common micronutrient deficiency associated with metabolic changes in the levels of iron regulatory proteins, hepcidin and ferroportin. Studies have associated dysregulation of iron homeostasis to other secondary and life-threatening diseases including anaemia, neurodegeneration and metabolic diseases. Iron deficiency plays a critical role in epigenetic regulation by affecting the Fe2+/α-ketoglutarate-dependent demethylating enzymes, Ten Eleven Translocase 1-3 (TET 1-3) and Jumonji-C (JmjC) histone demethylase, which are involved in epigenetic erasure of the methylation marks on both DNA and histone tails, respectively. In this review, studies involving epigenetic effects of iron deficiency associated with dysregulation of TET 1-3 and JmjC histone demethylase enzyme activities on hepcidin/ferroportin axis are discussed.
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