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通过全基因组RNAi鉴定的Notch转录活性调节剂。

Modifiers of notch transcriptional activity identified by genome-wide RNAi.

作者信息

Mourikis Philippos, Lake Robert J, Firnhaber Christopher B, DeDecker Brian S

机构信息

Stem Cells & Development, Department of Developmental Biology, Pasteur Institute, CNRS URA 2578, Paris, France.

出版信息

BMC Dev Biol. 2010 Oct 19;10:107. doi: 10.1186/1471-213X-10-107.

Abstract

BACKGROUND

The Notch signaling pathway regulates a diverse array of developmental processes, and aberrant Notch signaling can lead to diseases, including cancer. To obtain a more comprehensive understanding of the genetic network that integrates into Notch signaling, we performed a genome-wide RNAi screen in Drosophila cell culture to identify genes that modify Notch-dependent transcription.

RESULTS

Employing complementary data analyses, we found 399 putative modifiers: 189 promoting and 210 antagonizing Notch activated transcription. These modifiers included several known Notch interactors, validating the robustness of the assay. Many novel modifiers were also identified, covering a range of cellular localizations from the extracellular matrix to the nucleus, as well as a large number of proteins with unknown function. Chromatin-modifying proteins represent a major class of genes identified, including histone deacetylase and demethylase complex components and other chromatin modifying, remodeling and replacement factors. A protein-protein interaction map of the Notch-dependent transcription modifiers revealed that a large number of the identified proteins interact physically with these core chromatin components.

CONCLUSIONS

The genome-wide RNAi screen identified many genes that can modulate Notch transcriptional output. A protein interaction map of the identified genes highlighted a network of chromatin-modifying enzymes and remodelers that regulate Notch transcription. Our results open new avenues to explore the mechanisms of Notch signal regulation and the integration of this pathway into diverse cellular processes.

摘要

背景

Notch信号通路调控多种发育过程,Notch信号异常可导致包括癌症在内的多种疾病。为了更全面地了解整合到Notch信号中的遗传网络,我们在果蝇细胞培养中进行了全基因组RNA干扰筛选,以鉴定可调节Notch依赖性转录的基因。

结果

通过互补数据分析,我们发现了399个假定的调节因子:189个促进Notch激活转录,210个拮抗Notch激活转录。这些调节因子包括几个已知的Notch相互作用蛋白,验证了该检测方法的稳健性。还鉴定出许多新的调节因子,涵盖从细胞外基质到细胞核的一系列细胞定位,以及大量功能未知的蛋白质。染色质修饰蛋白是鉴定出的主要基因类别,包括组蛋白脱乙酰酶和去甲基酶复合物成分以及其他染色质修饰、重塑和置换因子。Notch依赖性转录调节因子的蛋白质-蛋白质相互作用图谱显示,大量鉴定出的蛋白质与这些核心染色质成分存在物理相互作用。

结论

全基因组RNA干扰筛选鉴定出许多可调节Notch转录输出的基因。鉴定出的基因的蛋白质相互作用图谱突出了一个由染色质修饰酶和重塑因子组成的网络,该网络调节Notch转录。我们的结果为探索Notch信号调节机制以及该信号通路如何整合到不同细胞过程中开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a65/2976970/d7bfc37432f1/1471-213X-10-107-1.jpg

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