Noncoding RNA gene silencing through genomic integration of RNA destabilizing elements using zinc finger nucleases

被引:132
作者
Gutschner, Tony [1 ,2 ]
Baas, Marion [1 ,2 ]
Diederichs, Sven [1 ,2 ]
机构
[1] German Canc Res Ctr, Helmholtz Univ Grp Mol RNA Biol & Canc, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Inst Pathol, D-69120 Heidelberg, Germany
关键词
CHROMATIN; CELLS; CLEAVAGE;
D O I
10.1101/gr.122358.111
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
Zinc finger nucleases (ZFNs) allow site-specific manipulation of the genome. So far, the use of ZFNs to create gene knockouts has been restricted to protein-coding genes. However, non-protein-encoding RNAs (ncRNA) play important roles in the cell, although the functions of most ncRNAs are unknown. Here, we describe a ZFN-based method suited for the silencing of protein-coding and noncoding genes. This method relies on the ZFN-mediated integration of RNA destabilizing elements into the human genome, e. g., poly(A) signals functioning as termination elements and destabilizing downstream sequences. The biallelic integration of poly(A) signals into the gene locus of the long ncRNA MALAT1 resulted in a 1000-fold decrease of RNA expression. Thus, this approach is more specific and 300 times more efficient than RNA interference techniques. The opportunity to create a variety of loss-of-function tumor model cell lines in different cancer backgrounds will promote future functional analyses of important long noncoding RNA transcripts.
引用
收藏
页码:1944 / 1954
页数:11
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