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天然和人工设计的微小RNA在人细胞中表达时均可抑制同源mRNA的表达。

Both natural and designed micro RNAs can inhibit the expression of cognate mRNAs when expressed in human cells.

作者信息

Zeng Yan, Wagner Eric J, Cullen Bryan R

机构信息

Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Mol Cell. 2002 Jun;9(6):1327-33. doi: 10.1016/s1097-2765(02)00541-5.

Abstract

Animal cells have recently been shown to express a range of approximately 22 nucleotide noncoding RNAs termed micro RNAs (miRNAs). Here, we show that the human mir-30 miRNA can be excised from irrelevant, endogenously transcribed mRNAs encompassing the predicted 71 nucleotide mir-30 precursor. Expression of the mir-30 miRNA specifically blocked the translation in human cells of an mRNA containing artificial mir-30 target sites. Similarly, designed miRNAs were also excised from transcripts encompassing artificial miRNA precursors and could inhibit the expression of mRNAs containing a complementary target site. These data indicate that novel miRNAs can be readily produced in vivo and can be designed to specifically inactivate the expression of selected target genes in human cells.

摘要

最近研究表明,动物细胞能表达一系列长度约为22个核苷酸的非编码RNA,称为微小RNA(miRNA)。在此,我们发现人类mir-30 miRNA可从无关的内源性转录mRNA中切除,这些mRNA包含预测的71个核苷酸的mir-30前体。mir-30 miRNA的表达特异性地阻断了含有人工mir-30靶位点的mRNA在人类细胞中的翻译。同样,设计的miRNA也可从包含人工miRNA前体的转录本中切除,并能抑制含有互补靶位点的mRNA的表达。这些数据表明,新型miRNA可在体内轻易产生,并且可设计用于特异性地使人类细胞中选定靶基因的表达失活。

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