Dnmt1 regulates the myogenic lineage specification of muscle stem cells

被引:17
|
作者
Liu, Renjing [1 ,2 ,3 ]
Kim, Kun-Yong [1 ]
Jung, Yong-Wook [1 ,4 ]
Park, In-Hyun [1 ]
机构
[1] Yale Sch Med, Yale Stem Cell Ctr, Dept Genet, 10 Amistad,201B, New Haven, CT 06520 USA
[2] Univ Sydney, Centenary Inst, Agnes Ginges Lab Dis Aorta, Camperdown, NSW 2042, Australia
[3] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
[4] CHA Univ, Dept Obstet & Gynecol, CHA Gangnam Med Ctr, Seoul, South Korea
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
美国国家卫生研究院;
关键词
DNA METHYLTRANSFERASE GENE; METHYLATION PATTERNS; HEMATOPOIETIC STEM; SELF-RENEWAL; DIFFERENTIATION; HYPOMETHYLATION; MECHANISMS; EXPRESSION; MUTATIONS; INDUCTION;
D O I
10.1038/srep35355
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA methylation is an important epigenetic mark that regulates gene expression. Dnmt1 plays an important role in maintaining DNA methylation patterns on daughter DNA strands. Studies have shed light into the functional role of Dnmt1 regulation in the hematopoietic and epidermal systems. Here we show that Dnmt1 is required for myogenesis. Loss of Dnmt1 results in reduced expression of myogenic genes and defects in myogenic differentiation. We have utilized a conditional knockout mouse approach to examine the functional consequences of Dnmt1 depletion specifically in the developing muscle. These mice were born runted, with smaller body weights, and reduced ability to form myotubes in vitro. We show that expression of Id-1, a negative regulator of myogenesis, is enhanced in Dnmt1-deficient cultures, leading to enhanced transdifferentiation of myoblasts toward the osteogenic lineage. Thus, these studies demonstrate that Dnmt1 influences cellular identity and determines lineage fidelity.
引用
收藏
页数:9
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