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果蝇胚胎中微小RNA基因表达的空间调控。

Spatial regulation of microRNA gene expression in the Drosophila embryo.

作者信息

Biemar Frédéric, Zinzen Robert, Ronshaugen Matthew, Sementchenko Victor, Manak J Robert, Levine Michael S

机构信息

Division of Genetics and Development, Department of Molecular Cell Biology, Center for Integrative Genomics, University of California, Berkeley, CA 94720, USA.

出版信息

Proc Natl Acad Sci U S A. 2005 Nov 1;102(44):15907-11. doi: 10.1073/pnas.0507817102. Epub 2005 Oct 25.

Abstract

MicroRNAs (miRNAs) regulate posttranscriptional gene activity by binding to specific sequences in the 3' UTRs of target mRNAs. A number of metazoan miRNAs have been shown to exhibit tissue-specific patterns of expression. Here, we investigate the possibility that localized expression is mediated by tissue-specific enhancers, comparable to those seen for protein-coding genes. Two miRNA loci in Drosophila melanogaster are investigated, the mir-309-6 polycistron (8-miR) and the mir-1 gene. The 8-miR locus contains a cluster of eight distinct miRNAs that are transcribed in a common precursor RNA. The 8-miR primary transcript displays a dynamic pattern of expression in early embryos, including repression at the anterior and posterior poles. An 800-bp 5' enhancer was identified that recapitulates this complex pattern when attached to a RNA polymerase II core promoter fused to a lacZ-reporter gene. The miR-1 locus is specifically expressed in the mesoderm of gastrulating embryos. Bioinformatics methods were used to identify a mesoderm-specific enhancer located approximately 5 kb 5' of the miR-1 transcription unit. Evidence is presented that the 8-miR enhancer is regulated by the localized Huckebein repressor, whereas miR-1 is activated by Dorsal and Twist. These results provide evidence that restricted activities of the 8-miR and miR-1 miRNAs are mediated by classical tissue-specific enhancers.

摘要

微小RNA(miRNA)通过与靶标mRNA的3'非翻译区(UTR)中的特定序列结合来调节转录后基因活性。许多后生动物的miRNA已被证明呈现出组织特异性的表达模式。在这里,我们研究了局部表达是否由组织特异性增强子介导的可能性,这与蛋白质编码基因的情况类似。我们研究了黑腹果蝇中的两个miRNA基因座,即mir-309-6多顺反子(8-miR)和mir-1基因。8-miR基因座包含一组八个不同的miRNA,它们在一个共同的前体RNA中被转录。8-miR初级转录本在早期胚胎中呈现出动态的表达模式,包括在前极和后极的抑制。我们鉴定出一个800 bp的5'增强子,当它连接到与lacZ报告基因融合的RNA聚合酶II核心启动子时,能重现这种复杂的模式。mir-1基因座在原肠胚形成胚胎的中胚层中特异性表达。我们使用生物信息学方法鉴定出一个位于mir-1转录单元5'端约5 kb处的中胚层特异性增强子。有证据表明,8-miR增强子受局部化的Huckebein阻遏物调控,而mir-1则由背腹蛋白(Dorsal)和扭转蛋白(Twist)激活。这些结果提供了证据,表明8-miR和mir-1 miRNA的受限活性是由经典的组织特异性增强子介导的。

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