{"title":"Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent.","authors":"Genhua Zheng, Victor Ambros, Wen-Hong Li","doi":"10.1186/1758-907X-1-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Antisense reagents can serve as efficient and versatile tools for studying gene function by inhibiting nucleic acids in vivo. Antisense reagents have particular utility for the experimental manipulation of the activity of microRNAs (miRNAs), which are involved in the regulation of diverse developmental and physiological pathways in animals. Even in traditional genetic systems, such as the nematode Caenorhabditis elegans, antisense reagents can provide experimental strategies complementary to mutational approaches. Presently no antisense reagents are available for inhibiting miRNAs in the nematode C. elegans.</p><p><strong>Results: </strong>We have developed a new class of fluorescently labelled antisense reagents to inhibit miRNAs in developing worms. These reagents were synthesized by conjugating dextran with 2'-O-methyl oligoribonucleotide. The dextran-conjugated antisense reagents can be conveniently introduced into the germline of adult hermaphrodites and are transmitted to their progeny, where they efficiently and specifically inhibit a targeted miRNA in different tissues, including the hypodermis, the vulva and the nervous system. We show that these reagents can be used combinatorially to inhibit more than one miRNA in the same animal.</p><p><strong>Conclusion: </strong>This class of antisense reagents represents a new addition to the toolkit for studying miRNA in C. elegans. Combined with numerous mutants or reporter stains available, these reagents should provide a convenient approach to examine genetic interactions that involve miRNA, and may facilitate studying functions of miRNAs, especially ones whose deletion strains are difficult to generate.See related research article: http://jbiol.com/content/9/3/20.</p>","PeriodicalId":88703,"journal":{"name":"Silence","volume":"1 1","pages":"9"},"PeriodicalIF":0.0000,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864223/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Silence","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/1758-907X-1-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Antisense reagents can serve as efficient and versatile tools for studying gene function by inhibiting nucleic acids in vivo. Antisense reagents have particular utility for the experimental manipulation of the activity of microRNAs (miRNAs), which are involved in the regulation of diverse developmental and physiological pathways in animals. Even in traditional genetic systems, such as the nematode Caenorhabditis elegans, antisense reagents can provide experimental strategies complementary to mutational approaches. Presently no antisense reagents are available for inhibiting miRNAs in the nematode C. elegans.
Results: We have developed a new class of fluorescently labelled antisense reagents to inhibit miRNAs in developing worms. These reagents were synthesized by conjugating dextran with 2'-O-methyl oligoribonucleotide. The dextran-conjugated antisense reagents can be conveniently introduced into the germline of adult hermaphrodites and are transmitted to their progeny, where they efficiently and specifically inhibit a targeted miRNA in different tissues, including the hypodermis, the vulva and the nervous system. We show that these reagents can be used combinatorially to inhibit more than one miRNA in the same animal.
Conclusion: This class of antisense reagents represents a new addition to the toolkit for studying miRNA in C. elegans. Combined with numerous mutants or reporter stains available, these reagents should provide a convenient approach to examine genetic interactions that involve miRNA, and may facilitate studying functions of miRNAs, especially ones whose deletion strains are difficult to generate.See related research article: http://jbiol.com/content/9/3/20.
背景:反义试剂在体内通过抑制核酸来研究基因功能是一种高效、通用的工具。反义试剂在实验操作microRNAs (miRNAs)的活性方面具有特殊的用途,这些microRNAs参与调节动物的多种发育和生理途径。即使在传统的遗传系统中,如秀丽隐杆线虫,反义试剂也可以提供与突变方法互补的实验策略。目前还没有能够抑制秀丽隐杆线虫mirna的反义试剂。结果:我们开发了一类新的荧光标记反义试剂来抑制发育中的蠕虫的miRNAs。这些试剂是通过右旋糖酐与2'- o -甲基寡核苷酸偶联合成的。右旋糖酐偶联反义试剂可以方便地导入雌雄同体的生殖系并传递给其后代,从而有效地特异性抑制不同组织中的靶向miRNA,包括皮下组织、外阴和神经系统。我们表明,这些试剂可以组合使用,以抑制一个以上的miRNA在同一动物。结论:这类反义试剂为研究秀丽隐杆线虫miRNA提供了新的工具。结合大量的突变体或可用的报告染色剂,这些试剂应该提供一种方便的方法来检查涉及miRNA的遗传相互作用,并可能有助于研究miRNA的功能,特别是那些难以产生缺失菌株的miRNA。参见相关研究文章:http://jbiol.com/content/9/3/20。