Epigenetic heterogeneity at imprinted loci in normal populations

被引:85
作者
Sakatani, T
Wei, M
Katoh, M
Okita, C
Wada, D
Mitsuya, K
Meguro, M
Ikeguchi, M
Ito, H
Tycko, B
Oshimura, M
机构
[1] Tottori Univ, Fac Med, Sch Life Sci, Dept Mol & Cell Genet, Tottori 6838503, Japan
[2] CREST, Program Japan Sci & Technol Corp, Yonago, Tottori, Japan
[3] Tottori Univ, Fac Med, Dept Pathol 1, Tottori 6838503, Japan
[4] Tottori Univ, Fac Med, Dept Surg 1, Tottori 6838503, Japan
[5] Columbia Univ, Coll Phys & Surg, Dept Pathol, New York, NY USA
[6] Columbia Univ, Coll Phys & Surg, Inst Canc Genet, New York, NY USA
关键词
epigenetic; genomic imprinting; IGF2; SNRPN; IMPT1;
D O I
10.1006/bbrc.2001.4916
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
Genomic imprinting is the phenomenon by which the two alleles of certain genes are differentially expressed according to their parental origin. Extensive analysis of allelic expression at multiple imprinted loci in a normal population has not performed so far. In the present study, we examined the allelic expression pattern of three imprinted genes in a panel of 262 Japanese normal individuals. We observed differences in the extent of maintenance of allele-specific expression of the three genes. The allelic expression of small nuclear ribonucleoprotein N (SNRPN) was stringently regulated while that of multimembrane-spanning polyspecific transporter-like gene 1 (IMPT1) showed a large degree of variation. Significant biallelic expression of insulin-like growth factor II (IGF2) was observed in about 10% of normal individuals. Our findings add to the accumulating evidence for variable allelic expression at multiple loci in a normal human population. This epigenetic heterogeneity can be a stable trait and potentially influence individual phenotypes. (C) 2001 Academic Press.
引用
收藏
页码:1124 / 1130
页数:7
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