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首页> 外文期刊>G3: Genes, Genomes, Genetics >Identification of Genes Interacting with rnt-1 Through Large-Scale RNAi Screening in Caenorhabditis elegans
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Identification of Genes Interacting with rnt-1 Through Large-Scale RNAi Screening in Caenorhabditis elegans

机译:通过秀丽隐杆线虫的大规模RNAi筛选鉴定与rnt-1相互作用的基因。

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Although many critical roles of the RUNX family proteins have already been identified, little attention has been given to how these proteins interact with other factors. Elucidating RUNX protein interactions will help extend our understanding of their roles in normal development and tumorigenesis. In this study, we performed large-scale RNAi screening to identify genes that genetically interact with [rnt-1][1] , the sole homolog of RUNX protein in the nematode Caenorhabditis elegans . To this end, we took advantage of the fact that C. elegans can survive a severe loss of [RNT-1][2] function with only mild phenotypes, and we looked for genes that caused a synthetic phenotype in the [rnt-1][1] mutant background. We identified seven genes, three of which ( [cdk-8][3] , [cic-1][4] , and [sur-2][5] ) are involved in transcription, two of which ( [pgp-2][6] and [cct-5][7] ) are involved in stress response, and two of which ([D2045.7][8] and [W09D10.4][9]) are involved in signaling cascades, according to their functional gene ontology terms. We further confirmed that the CDK8-containing mediator complex genetically interacts with [RNT-1][2] by showing that knockdown of each component of the CDK8 mediator complex caused a synthetic phenotype, that is, the exploded intestine through the vulva (Eiv) phenotype, in the [rnt-1][1] mutant background. We also identified a putative target gene, [acs-4][10] , which is regulated by the [RNT-1][2] and CDK8 mediator complex. Our results strengthen the notion that the CDK8 mediator complex may also act together with RUNX proteins in mammals. [1]: http://www.wormbase.org/db/get?name=rnt-1;class=Gene [2]: http://www.wormbase.org/db/get?name=RNT-1;class=Gene [3]: http://www.wormbase.org/db/get?name=cdk-8;class=Gene [4]: http://www.wormbase.org/db/get?name=cic-1;class=Gene [5]: http://www.wormbase.org/db/get?name=sur-2;class=Gene [6]: http://www.wormbase.org/db/get?name=pgp-2;class=Gene [7]: http://www.wormbase.org/db/get?name=cct-5;class=Gene [8]: http://www.wormbase.org/db/get?name=D2045.7;class=Gene [9]: http://www.wormbase.org/db/get?name=W09D10.4;class=Gene [10]: http://www.wormbase.org/db/get?name=acs-4;class=Gene.
机译:尽管已经确定了RUNX家族蛋白的许多关键作用,但很少关注这些蛋白如何与其他因素相互作用。阐明RUNX蛋白相互作用将有助于扩展我们对它们在正常发育和肿瘤发生中作用的理解。在这项研究中,我们进行了大规模的RNAi筛选,以鉴定与[rnt-1] [1](线虫秀丽隐杆线虫中RUNX蛋白的唯一同源物)进行基因相互作用的基因。为此,我们利用了秀丽隐杆线虫只能在轻度表型的情况下存活[RNT-1] [2]功能的严重损失这一事实,并寻找在[rnt-1]中引起合成表型的基因] [1]突变背景。我们鉴定了七个基因,其中三个([cdk-8] [3],[cic-1] [4]和[sur-2] [5])参与转录,其中两个([pgp-2 ] [6]和[cct-5] [7])参与了压力响应,其中两个([D2045.7] [8]和[W09D10.4] [9])与信号级联有关。他们的功能基因本体论术语。我们进一步证实了包含CDK8的介体复合物与[RNT-1] [2]发生了遗传相互作用,这表明CDK8介体复合物的每个组成部分的敲除都导致了合成表型,即通过外阴的肠道爆炸(Eiv)表型,在[rnt-1] [1]突变背景中。我们还确定了推定的靶基因[acs-4] [10],该基因受[RNT-1] [2]和CDK8介体复合物的调控。我们的结果强化了CDK8介体复合物也可能与RUNX蛋白一起在哺乳动物中起作用的观念。 [1]:http://www.wormbase.org/db/get?name=rnt-1;class=Gene [2]:http://www.wormbase.org/db/get?name=RNT-1 ; class = Gene [3]:http://www.wormbase.org/db/get?name=cdk-8;class=Gene [4]:http://www.wormbase.org/db/get?name = cic-1; class = Gene [5]:http://www.wormbase.org/db/get?name = sur-2; class = Gene [6]:http://www.wormbase.org/db / get?name = pgp-2; class = Gene [7]:http://www.wormbase.org/db/get?name=cct-5;class=Gene [8]:http://www.wormbase .org / db / get?name = D2045.7; class =基因[9]:http://www.wormbase.org/db/get?name=W09D10.4;class=Gene [10]:http:// /www.wormbase.org/db/get?name=acs-4;class=Gene。

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