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反义寡核苷酸介导的斑马鱼转录本敲低

Antisense Oligonucleotide-Mediated Transcript Knockdown in Zebrafish.

作者信息

Pauli Andrea, Montague Tessa G, Lennox Kim A, Behlke Mark A, Schier Alexander F

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, Masschusetts, United States of America.

Integrated DNA Technologies, Inc., Coralville, Iowa, United States of America.

出版信息

PLoS One. 2015 Oct 5;10(10):e0139504. doi: 10.1371/journal.pone.0139504. eCollection 2015.

Abstract

Antisense oligonucleotides (ASOs) are synthetic, single-strand RNA-DNA hybrids that induce catalytic degradation of complementary cellular RNAs via RNase H. ASOs are widely used as gene knockdown reagents in tissue culture and in Xenopus and mouse model systems. To test their effectiveness in zebrafish, we targeted 20 developmental genes and compared the morphological changes with mutant and morpholino (MO)-induced phenotypes. ASO-mediated transcript knockdown reproduced the published loss-of-function phenotypes for oep, chordin, dnd, ctnnb2, bmp7a, alk8, smad2 and smad5 in a dosage-sensitive manner. ASOs knocked down both maternal and zygotic transcripts, as well as the long noncoding RNA (lncRNA) MALAT1. ASOs were only effective within a narrow concentration range and were toxic at higher concentrations. Despite this drawback, quantitation of knockdown efficiency and the ability to degrade lncRNAs make ASOs a useful knockdown reagent in zebrafish.

摘要

反义寡核苷酸(ASOs)是一种合成的单链RNA-DNA杂交分子,可通过核糖核酸酶H诱导互补细胞RNA的催化降解。ASOs在组织培养以及非洲爪蟾和小鼠模型系统中被广泛用作基因敲低试剂。为了测试它们在斑马鱼中的有效性,我们靶向了20个发育基因,并将形态变化与突变体和吗啉代(MO)诱导的表型进行了比较。ASO介导的转录本敲低以剂量敏感的方式重现了已发表的oep、脊索蛋白、dnd、ctnnb2、bmp7a、alk8、smad2和smad5功能丧失表型。ASOs敲低了母源和zygotic转录本以及长链非编码RNA(lncRNA)MALAT1。ASOs仅在狭窄的浓度范围内有效,在较高浓度下具有毒性。尽管有这个缺点,但敲低效率的定量和降解lncRNAs的能力使ASOs成为斑马鱼中一种有用的敲低试剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1679/4593562/038ce62b55ad/pone.0139504.g001.jpg

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