GSTDTAP  > 地球科学
DOI10.1126/science.aah7111
CRISPRi-based genome-scale identification of functional long noncoding RNA loci in human cells
Liu, S. John1,2; Horlbeck, Max A.3,4,5,6; Cho, Seung Woo9; Birk, Harjus S.1,2; Malatesta, Martina1,2; He, Daniel1,2; Attenello, Frank J.1,2; Villalta, Jacqueline E.3,4,5,6; Cho, Min Y.3,4,5,6; Chen, Yuwen3,4,5,6; Mandegar, Mohammad A.3; Olvera, Michael P.3; Gilbert, Luke A.3,4,5,6; Conklin, Bruce R.3,7,8; Chang, Howard Y.9; Weissman, Jonathan S.3,4,5,6; Lim, Daniel A.1,2,10
2017-01-06
发表期刊SCIENCE
ISSN0036-8075
EISSN1095-9203
出版年2017
卷号355期号:6320
文章类型Article
语种英语
国家USA
英文摘要

The human genome produces thousands of long noncoding RNAs (lncRNAs)-transcripts >200 nucleotides long that do not encode proteins. Although critical roles in normal biology and disease have been revealed for a subset of lncRNAs, the function of the vast majority remains untested. We developed a CRISPR interference (CRISPRi) platform targeting 16,401 lncRNA loci in seven diverse cell lines, including six transformed cell lines and human induced pluripotent stem cells (iPSCs). Large-scale screening identified 499 lncRNA loci required for robust cellular growth, of which 89% showed growth-modifying function exclusively in one cell type. We further found that lncRNA knockdown can perturb complex transcriptional networks in a cell type-specific manner. These data underscore the functional importance and cell type specificity of many lncRNAs.


领域地球科学 ; 气候变化 ; 资源环境
收录类别SCI-E
WOS记录号WOS:000391739900002
WOS关键词GENE-EXPRESSION ; STEM-CELLS ; DIFFERENTIATION ; TRANSCRIPTION ; EVOLUTION ; CANCER ; LNCRNA ; INTERFERENCE ; ACTIVATION ; ENHANCERS
WOS类目Multidisciplinary Sciences
WOS研究方向Science & Technology - Other Topics
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文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/195154
专题地球科学
资源环境科学
气候变化
作者单位1.Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA;
2.Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA;
3.Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA;
4.Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA;
5.Univ Calif San Francisco, Calif Inst Quantitat Biomed Res, San Francisco, CA 94143 USA;
6.Univ Calif San Francisco, Ctr RNA Syst Biol, San Francisco, CA 94143 USA;
7.Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA;
8.Gladstone Inst Cardiovasc Dis, San Francisco, CA USA;
9.Stanford Univ, Ctr Personal Dynam Regulomes, Stanford, CA 94305 USA;
10.San Francisco VA Med Ctr, San Francisco, CA USA
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Liu, S. John,Horlbeck, Max A.,Cho, Seung Woo,et al. CRISPRi-based genome-scale identification of functional long noncoding RNA loci in human cells[J]. SCIENCE,2017,355(6320).
APA Liu, S. John.,Horlbeck, Max A..,Cho, Seung Woo.,Birk, Harjus S..,Malatesta, Martina.,...&Lim, Daniel A..(2017).CRISPRi-based genome-scale identification of functional long noncoding RNA loci in human cells.SCIENCE,355(6320).
MLA Liu, S. John,et al."CRISPRi-based genome-scale identification of functional long noncoding RNA loci in human cells".SCIENCE 355.6320(2017).
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