Re-investigation and RNA sequencing-based identification of genes with placenta-specific imprinted expression

被引:94
作者
Okae, Hiroaki
Hiura, Hitoshi
Nishida, Yuichiro [2 ]
Funayama, Ryo [2 ]
Tanaka, Satoshi [3 ]
Chiba, Hatsune [4 ]
Yaegashi, Nobuo [5 ]
Nakayama, Keiko [2 ]
Sasaki, Hiroyuki [4 ]
Arima, Takahiro [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Informat Genet, Environm & Genome Res Ctr,Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Grad Sch Med, Div Cell Proliferat, United Ctr Adv Res & Translat Med, Sendai, Miyagi 9808575, Japan
[3] Univ Tokyo, Dept Anim Resource Sci Vet Med Sci, Lab Cellular Biochem, Tokyo 1138657, Japan
[4] Kyushu Univ, Med Inst Bioregulat, Dept Mol Genet, Fukuoka 8128582, Japan
[5] Tohoku Univ, Dept Obstet & Gynecol, Grad Sch Med, Sendai, Miyagi 9808574, Japan
基金
日本学术振兴会;
关键词
REPRESSIVE HISTONE METHYLATION; MOUSE PROXIMAL CHROMOSOME-6; ORIGIN ALLELIC EXPRESSION; EXTRAEMBRYONIC TISSUES; WIDE IDENTIFICATION; DNA METHYLATION; GROWTH-FACTOR; IN-VIVO; DOMAIN; INACTIVATION;
D O I
10.1093/hmg/ddr488
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
Within the vertebrate groups, only mammals are subject to a specialized epigenetic process termed genomic imprinting in which genes are preferentially expressed from one parental allele. Imprinted expression has been reported for >100 mouse genes and, for approximately one-quarter of these genes, the imprinted expression is specific to the placenta (or extraembryonic tissues). This seemingly placenta-specific imprinted expression has garnered much attention, as has the apparent lack of conserved imprinting between the human and mouse placenta. In this study, we used a novel approach to re-investigate the placenta-specific expression using embryo transfer and trophoblast stem cells. We analyzed 20 genes previously reported to show maternal allele-specific expression in the placenta, and only 8 genes were confirmed to be imprinted. Other genes were likely to be falsely identified as imprinted due to their relatively high expression in contaminating maternal cells. Next, we performed a genome-wide transcriptome assay and identified 133 and 955 candidate imprinted genes with paternal allele- and maternal allele-specific expression. Of those we analyzed in detail, 1/6 (Gab1) of the candidates for paternal allele-specific expression and only 1/269 (Ano1) candidates for maternal allele-specific expression were authentically imprinted genes. Imprinting of Ano1 and Gab1 was specific to the placenta and neither gene displayed allele-specific promoter DNA methylation. Imprinting of ANO1, but not GAB1, was conserved in the human placenta. Our findings impose a considerable revision of the current views of placental imprinting.
引用
收藏
页码:548 / 558
页数:11
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