Epigenetic regulation of thyroid hormone-induced adult intestinal stem cell development during anuran metamorphosis

被引:28
作者
Sun, Guihong [1 ]
Fu, Liezhen [2 ]
Shi, Yun-Bo [2 ]
机构
[1] Wuhan Univ, Sch Basic Med Sci, Wuhan 430072, Peoples R China
[2] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Mol Morphogenesis, PCRM, NIH, Bethesda, MD 20892 USA
基金
中国国家自然科学基金;
关键词
Thyroid hormone receptor; Stem cell; Metamorphosis; Xenopus laevis and tropicalis; Histone methylation; Histone acetylation; Intestine; RECEPTOR-MEDIATED TRANSCRIPTION; ARGININE METHYLTRANSFERASE 1; EFFECTOR NUCLEASES TALENS; TARGETED GENE DISRUPTION; XENOPUS-LAEVIS; AMPHIBIAN METAMORPHOSIS; HISTONE H3; POSTEMBRYONIC DEVELOPMENT; COREPRESSOR COMPLEX; CO-REPRESSOR;
D O I
10.1186/2045-3701-4-73
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epigenetic modifications of histones are emerging as key factors in gene regulation by diverse transcription factors. Their roles during vertebrate development and pathogenesis are less clear. The causative effect of thyroid hormone (T3) on amphibian metamorphosis and the ability to manipulate this process for molecular and genetic studies have led to the demonstration that T3 receptor (TR) is necessary and sufficient for Xenopus metamorphosis, a process that resembles the postembryonic development (around birth) in mammals. Importantly, analyses during metamorphosis have provided some of the first in vivo evidence for the involvement of histone modifications in gene regulation by TR during vertebrate development. Furthermore, expression and functional studies suggest that various histone modifying epigenetic enzymes likely participate in multiple steps during the formation of adult intestinal stem cells during metamorphosis. The similarity between intestinal remodeling and the maturation of the mammalian intestine around birth when T3 levels are high suggests conserved roles for the epigenetic enzymes in mammalian adult intestinal stem cell development and/ or proliferation.
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页数:8
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