生物
骨骼肌
C2C12型
基因剔除小鼠
内分泌学
心肌细胞
内科学
下调和上调
基因敲除
等位基因
基因表达
肌肉团
基因
肌发生
遗传学
医学
作者
Ling Liu,Shengnan Wang,Wenjie Tian,Cheng Xu,Chengjie Wei,Kai Cui,Lin Jiang,Dandan Wang
出处
期刊:Biology
[Multidisciplinary Digital Publishing Institute]
日期:2023-02-17
卷期号:12 (2): 325-325
被引量:5
标识
DOI:10.3390/biology12020325
摘要
ZBED6, a key transcription factor, plays an important role in skeletal muscle and organ growth. ZBED6 knockout (ZBED6-/-) leads to the upregulation of IGF2 in pig and mice muscle, thereby increasing muscle mass. However, the effects and mechanism of Zbed6 single-allele knockout (Zbed6+/-) on mice muscle remain unknown. Here, we reported that Zbed6+/- promotes muscle growth by a new potential target gene rather than Igf2 in mice muscle. Zbed6+/- mice showed markedly higher muscle mass (25%) and a markedly higher muscle weight ratio (18%) than wild-type (WT) mice, coinciding with a larger muscle fiber area (28%). Despite a significant increase in muscle growth, Zbed6+/- mice showed similar Igf2 expression with WT mice, indicating that a ZBED6-Igf2-independent regulatory pathway exists in Zbed6+/- mice muscle. RNA-seq of muscle between the Zbed6+/- and WT mice revealed two terms related to muscle growth. Overlapping the DEGs and C2C12 Chip-seq data of ZBED6 screened out a potential ZBED6 target gene Barx2, which may regulate muscle growth in Zbed6+/- mice. These results may open new research directions leading to a better understanding of the integral functions of ZBED6 and provide evidence of Zbed6+/- promoting muscle growth by regulating Barx2 in mice.
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