Promoter-specific insulin-like growth factor 2 gene imprinting in human fetal liver and hepatoblastoma

被引:0
|
作者
Yun, K
Jinno, Y
Sohda, T
Niikawa, N
Ikeda, T
机构
[1] Univ Otago, Sch Med, Dept Pathol, Canc Res Lab, Dunedin, New Zealand
[2] Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 852, Japan
[3] Fukuoka Univ, Sch Med, Dept Internal Med 1, Fukuoka 81480, Japan
[4] Nagasaki Univ, Sch Med, Dept Pathol 1, Nagasaki 852, Japan
来源
JOURNAL OF PATHOLOGY | 1998年 / 185卷 / 01期
关键词
genomic imprinting; IGF2; H19; promoter usage; RT-PCR; in situ hybridization; fetal liver; hepatoblastoma;
D O I
10.1002/(SICI)1096-9896(199805)185:1<91::AID-PATH44>3.0.CO;2-K
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Insulin-like growth factor 2 (IGF2) gene imprinting has been demonstrated to be promoter-specific, in that expression from the P1 promoter is biallelic whereas that from the P2-P4 promoters is monoallelic, In the present study, in order to investigate IGF2 gene imprinting status at the cellular level, allelic analysis was performed of IGF2 gene expression transcribed from the P1 and P3 promoters, using reverse transcription polymerase chain reaction (RT-PCR) on human fetal liver and hepatoblastoma. In situ hybridization was also undertaken, to obtain information about the cellular localization of transcripts expressed from the P1 and P3 promoters. The results indicated that transcripts expressed from the P1 and P3 promoters co-localized in the same fetal or neoplastic hepatocytes, These data should provide information regarding the molecular basis of genomic imprinting, suggesting that an imprint recognized for the differential expression may be strictly local and localized downstream of the IGF2 P1 promoter. (C) 1998 John Wiley & Sons, Ltd.
引用
收藏
页码:91 / 98
页数:8
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