生物
脱甲基酶
再生(生物学)
热空气
Hox基因
心脏发育
RNA干扰
癌症研究
去甲基化
基因敲除
长非编码RNA
下调和上调
表观遗传学
DNA甲基化
细胞生物学
核糖核酸
内科学
基因表达
胚胎干细胞
基因
遗传学
医学
作者
Qiaoman Fei,Manman Qiu,Guanwei Fan,Bo Zhang,Qin Wang,Sipei Zhang,Shuying Wang,Bing Yang,Ling Zhang
标识
DOI:10.1089/dna.2021.0095
摘要
Previous studies have shown that lysine-specific demethylase 1 (LSD1) could regulate cell cycle progression through demethylation. The 3′domain of HOX transcript antisense RNA (Hotair) combined with the LSD1/CoREST/REST complex helps LSD1 target the corresponding gene. However, its role in mice's myocardial regeneration is still unclear. The heart from neonatal mice shows strong myocardial regeneration ability, but this ability disappears 7 days after birth. Our study shows that the myocardial tissue highly expresses Hotair and Lsd1 within 1 week after birth, consistent with the myocardial regeneration time window. Knockdown Lsd1 or Hotair expression by RNA interference could inhibit myocardial regeneration and cardiomyocyte proliferation. Our results suggest that Hotair-mediated demethylation of LSD1 may play an important role in myocardial regeneration in neonatal mice.
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