Spatiotemporal expression of Prdm genes during Xenopus development

被引:8
|
作者
Eguchi, Rieko [1 ]
Yoshigai, Emi [2 ]
Koga, Takamasa [2 ]
Kuhara, Satoru [1 ,2 ]
Tashiro, Kosuke [1 ,2 ]
机构
[1] Kyushu Univ, Grad Sch Syst Life Sci, Higashi Ku, Fukuoka, Fukuoka 8128581, Japan
[2] Kyushu Univ, Grad Sch Bioresource & Bioenvironm Sci, Higashi Ku, Fukuoka, Fukuoka 8128581, Japan
关键词
Epigenetics; Neural development; Prdm; Xenopus embryos; HISTONE ARGININE METHYLATION; CENTRAL-NERVOUS-SYSTEM; CELL PROLIFERATION; MOUSE DEVELOPMENT; METHYLTRANSFERASE; DIFFERENTIATION; HETEROCHROMATIN; MAINTENANCE; FAMILY; STEM;
D O I
10.1007/s10616-015-9846-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Epigenetic regulation is known to be important in embryonic development, cell differentiation and regulation of cancer cells. Molecular mechanisms of epigenetic modification have DNA methylation and histone tail modification such as acetylation, phosphorylation and ubiquitination. Until now, many kinds of enzymes that modify histone tail with various functional groups have been reported and regulate the epigenetic state of genes. Among them, Prdm genes were identified as histone methyltransferase. Prdm genes are characterized by an N-terminal PR/SET domain and C-terminal some zinc finger domains and therefore they are considered to have both DNA-binding ability and methylation activity. Among vertebrate, fifteen members are estimated to belong to Prdm genes family. Even though Prdm genes are thought to play important roles for cell fate determination and cell differentiation, there is an incomplete understanding of their expression and functions in early development. Here, we report that Prdm genes exhibit dynamic expression pattern in Xenopus embryogenesis. By whole mount in situ hybridization analysis, we show that Prdm genes are expressed in spatially localized manners in embryo and all of Prdm genes are expressed in neural cells in developing central nervous systems. Our study suggests that Prdm genes may be new candidates to function in neural cell differentiation.
引用
收藏
页码:711 / 719
页数:9
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