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首页> 外文期刊>Bulletin of the Korean Chemical Society >Identification of B52-dependent Gene Expression Signature and Alternative Splicing Using a D. melanogaster B52-null Mutant
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Identification of B52-dependent Gene Expression Signature and Alternative Splicing Using a D. melanogaster B52-null Mutant

机译:B.依赖的基因表达特征的鉴定和D. melanogaster B52-null突变体的选择性剪接

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SR proteins are essential splicing regulators and also modulate alternative splicing events, which function both as redundant and substrate-specific manner. The Drosophila B52/SRp55, a member of the SR protein family, is essential for the fly development in vivo, as deletion of B52 gene results in lethality of animals at the second instar larval stage. Identification of the splicing target genes of B52 thus should be crucial for the understanding of the specific developmental role of B52 in vivo. In this study, we performed whole-genome DNA microarray experiments with a B52- knock-out animal. Analysis of the microarray data not only provided the B52-dependent gene expression signature, but also revealed a larval-stage specific, alternative splicing target gene of B52. Our result thus provides a starting point to understand the essential function of B52 at the organismal level.
机译:SR蛋白是必不可少的剪接调节剂,还可以调节其他剪接事件,这些剪接事件既具有冗余功能,又具有特定于底物的功能。果蝇B52 / SRp55是SR蛋白家族的一员,对于体内果蝇的发育至关重要,因为B52基因的缺失导致第二龄幼虫阶段的动物致死性。因此,鉴定B52的剪接靶基因对于了解B52在体内的特定发育作用至关重要。在这项研究中,我们对B52基因敲除动物进行了全基因组DNA微阵列实验。对微阵列数据的分析不仅提供了B52依赖的基因表达特征,而且还揭示了B52的幼虫期特异性,可变剪接靶基因。因此,我们的结果提供了一个起点,以了解B52在机体水平上的基本功能。

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