Mol. Cells 2008; 25(2): 211-215
Published online January 1, 1970
© The Korean Society for Molecular and Cellular Biology
To gain a better understanding of the methylation imprinting changes associated with heat stress in early development, we used bisulfite sequencing and bisulfite restriction analysis to examine the DNA methylation status of imprinted genes in early embryos (blastocysts). The paternal imprinted genes, H19 and Igf-2r, had lower methylation levels in heat-stressed embryos than in control embryos, whereas the maternal imprinted genes, Peg3 and Peg1, had similar methylation pattern in heat-stressed embryos and in control embryos. Our results indicate that heat stress may induce aberrant methylation imprinting, which results in developmental failure of mouse embryos, and that the effects of heat shock on methylation imprinting may be gene-specific.
Keywords Heat Stress, Methylation Imprinting, Mouse Embryos
Mol. Cells 2008; 25(2): 211-215
Published online April 30, 2008
Copyright © The Korean Society for Molecular and Cellular Biology.
Jia-Qiao Zhu, Jing-He Liu, Xing-Wei Liang, Bao-Zeng Xu, Yi Hou, Xing-Xu Zhao and Qing-Yuan Sun
To gain a better understanding of the methylation imprinting changes associated with heat stress in early development, we used bisulfite sequencing and bisulfite restriction analysis to examine the DNA methylation status of imprinted genes in early embryos (blastocysts). The paternal imprinted genes, H19 and Igf-2r, had lower methylation levels in heat-stressed embryos than in control embryos, whereas the maternal imprinted genes, Peg3 and Peg1, had similar methylation pattern in heat-stressed embryos and in control embryos. Our results indicate that heat stress may induce aberrant methylation imprinting, which results in developmental failure of mouse embryos, and that the effects of heat shock on methylation imprinting may be gene-specific.
Keywords: Heat Stress, Methylation Imprinting, Mouse Embryos
Su Jin Jang, Sung Hae Shin, Sung Tae Yee, Baek Hwang, Kyung Hoan Im, Ky Young Park
Mol. Cells 2005; 20(1): 136-141