A TRiP RNAi screen to identify molecules necessary for Drosophila photoreceptor differentiation.

IF 2.2
Johnathan Rylee, Simpla Mahato, John Aldrich, Emma Bergh, Brandon Sizemore, Lauren E Feder, Shaun Grega, Kennedy Helms, Megan Maar, Steven G Britt, Andrew C Zelhof
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引用次数: 1

Abstract

Drosophila rhabdomeric terminal photoreceptor differentiation is an extended process taking several days to complete. Following ommatidial patterning by the morphogenetic furrow, photoreceptors are sequentially recruited and specified, and terminal differentiation begins. Key events of terminal differentiation include the establishment of apical and basolateral domains, rhabdomere and stalk formation, inter-rhabdomeral space formation, and expression of phototransduction machinery. While many key regulators of these processes have been identified, the complete network of transcription factors to downstream effector molecules necessary for regulating each of these major events remains incomplete. Here, we report an RNAi screen to identify additional molecules and cellular pathways required for photoreceptor terminal differentiation. First, we tested several eye-specific GAL4 drivers for correct spatial and temporal specificity and identified Pph13-GAL4 as the most appropriate GAL4 line for our screen. We screened lines available through the Transgenic RNAi Project and isolated lines that when combined with Pph13-GAL4 resulted in the loss of the deep pseudopupil, as a readout for abnormal differentiation. In the end, we screened 6,189 lines, representing 3,971 genes, and have identified 64 genes, illuminating potential new regulatory molecules and cellular pathways for the differentiation and organization of Drosophila rhabdomeric photoreceptors.

Abstract Image

Abstract Image

Abstract Image

利用TRiP RNAi筛选果蝇光感受器分化所需分子。
果蝇横纹肌末端光感受器分化是一个漫长的过程,需要数天才能完成。通过形态发生沟,光感受器依次被募集和指定,终末分化开始。终末分化的关键事件包括顶端和底外侧结构域的建立、横纹肌和茎的形成、横纹肌间隙的形成以及光导机制的表达。虽然已经确定了这些过程的许多关键调节因子,但调节这些主要事件所需的转录因子到下游效应分子的完整网络仍然不完整。在这里,我们报告了一个RNAi筛选,以确定光感受器末端分化所需的额外分子和细胞途径。首先,我们测试了几种眼睛特异性GAL4驱动程序,以确定正确的空间和时间特异性,并确定Pph13-GAL4是最适合我们屏幕的GAL4系。我们通过转基因RNAi项目筛选了可获得的细胞系,并分离了与Pph13-GAL4结合导致深层假瞳孔缺失的细胞系,作为异常分化的读数。最后,我们筛选了6189个细胞系,代表3971个基因,并鉴定了64个基因,揭示了果蝇横纹肌光感受器分化和组织的潜在新调控分子和细胞途径。
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