A nucleolar protein, H19 opposite tumor suppressor (HOTS), is a tumor growth inhibitor encoded by a human imprinted H19 antisense transcript

被引:77
作者
Onyango, Patrick
Feinberg, Andrew P. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Ctr Epigenet, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
antisense RNA; DNA methylation; epigenetics; genomic; imprinting; BECKWITH-WIEDEMANN-SYNDROME; CHROMOSOME; 11P15; NONCODING RNA; GENE; METHYLATION; IGF2; EXPRESSION; DELETION; REGION; IDENTIFICATION;
D O I
10.1073/pnas.1110904108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The H19 gene, which localizes within a chromosomal region on human chromosome 11p15 that is commonly lost in Wilms tumor (WT), encodes an imprinted untranslated RNA. However, the biological significance of the H19 noncoding transcript remains unresolved because replacement of the RNA transcript with a neocassette has no obvious phenotypic effect. Here we show that the human H19 locus also encodes a maternally expressed, translated gene, antisense to the known H19 transcript, which is conserved in primates. This gene, termed HOTS for H19 opposite tumor suppressor, encodes a protein that localizes to the nucleus and nucleolus and that interacts with the human enhancer of rudimentary homolog (ERH) protein. WTs that show loss of heterozygosity of 11p15 or loss of imprinting of IGF2 also silence HOTS (7/7 and 10/10, respectively). Overexpression of HOTS inhibits Wilms, rhabdoid, rhabdomyosarcoma, and choriocarcinoma tumor cell growth, and silencing HOTS by RNAi increases in vitro colony formation and in vivo tumor growth. These results demonstrate that the human H19 locus harbors an imprinted gene encoding a tumor suppressor protein within the long-sought WT2 locus.
引用
收藏
页码:16759 / 16764
页数:6
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