4.5 Article

Effects of Ten-Eleven Translocation-2 (Tet2) on myogenic differentiation of chicken myoblasts

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cbpb.2020.110540

Keywords

DNA demethylation; Histone demethylation; MRFs; Myoblast differentiation; Tet2

Funding

  1. Fundamental Research Funds for the Central Universities [KYZ201724]
  2. National Natural Science Foundation of China [31402074]

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Tet2 plays a crucial role in chicken myogenesis by regulating the demethylation of genomic DNA and histones to control the expression of MRFs, thus contributing to myoblast differentiation. The expression of Tet2 is significantly elevated during myoblast differentiation, leading to an increase in 5hmC levels and a decrease in H3K9me2 and H3K27me3 levels. Knockdown of Tet2 inhibits the formation of multinucleated myotubes and reduces pivotal MRFs expression.
Skeletal muscle development is an orchestrated progress that is primarily regulated by tempomspatial expression of myogenic regulatory factors (MRFs). Recent studies demonstrated that DNA demethylation also exerted a critical role in myogenesis. However, the function of Tet2 in the regulation of chicken myogenesis still remains unknown. In the present study, the role of Tet2 in regulating myogenic differentiation was determined by using a model of primary myoblasts from chickens. The expression of Tet2 was significantly elevated during myoblast differentiation. Meanwhile, the level of 5hmC in genomic DNA was increased, but H3K9me2 and H3K27me3 were markedly reduced following differentiation. Knockdown of Tet2 significantly inhibited the formation of multinucleated myotubes, which was accompanied by a reduction of relevant pivotal MRFs. Moreover, the level of 5hmC decreased sharply in Tet2 knockdown myoblasts. Attenuated differentiated myoblasts that resulted from reduced Tet2 also demonstrated an increased level of H3K9me2 and H3K27me3. Collectively, these results indicated that Tet2 played an essential role during myogenesis, which affected demethylation of genomic DNA and histone to regulate expression of MRFs and therefore, contributed to myoblast differentiation.

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