Identification of JAK/STAT pathway regulators-Insights from RNAi screens

被引:23
作者
Mueller, Patrick [2 ]
Boutros, Michael [3 ]
Zeidler, Martin P. [1 ]
机构
[1] Univ Sheffield, Dept Biomed Sci, Ctr Dev & Biomed Genet, Sheffield S10 2TN, S Yorkshire, England
[2] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[3] German Canc Res Ctr, D-69120 Heidelberg, Germany
基金
英国医学研究理事会;
关键词
RNAi; Genome-wide screen; Cell culture; Luciferase reporter; Drosophila;
D O I
10.1016/j.semcdb.2008.06.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
While many core JAK/STAT pathway components have been discovered in Drosophila via classical genetic approaches, the identification of pathway regulators has been more challenging. Recently two cell-based RNAi screens for JAK/STAT pathway regulators have been undertaken using libraries of double-stranded RNAs targeting a large proportion of the predicted Drosophila transcriptome. While both screens identified multiple regulators, only relatively few loci are common to both data sets. Here we compare the two screens and discuss these differences. Although many factors are likely to be contributory, differences in the assay design are of key importance. Low levels of stimulation favouring the identification of negative pathway regulators and high levels of stimulation favouring the identification of positively acting factors. Ultimately, the results from both screens are likely to be largely complementary and have identified a range of novel candidate regulators of JAK/STAT pathway activity as a starting point for new research directions in the future. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:360 / 369
页数:10
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