Laboratory of Behavioral and Developmental Genetics, Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.
Centre for Functional Genomics, Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brooks University, Headington Campus, Oxford, United Kingdom.
PLoS Genet. 2022 Sep 12;18(9):e1010380. doi: 10.1371/journal.pgen.1010380. eCollection 2022 Sep.
Drosophila Insulin-Producing Cells (IPCs) are the main production site of the Drosophila Insulin-like peptides or dilps which have key roles in regulating growth, development, reproduction, lifespan and metabolism. To better understand the signalling pathways and transcriptional networks that are active in the IPCs we queried publicly available transcriptome data of over 180 highly inbred fly lines for dilp expression and used dilp expression as the input for a Genome-wide association study (GWAS). This resulted in the identification of variants in 125 genes that were associated with variation in dilp expression. The function of 57 of these genes in the IPCs was tested using an RNAi-based approach. We found that IPC-specific depletion of most genes resulted in differences in expression of one or more of the dilps. We then elaborated further on one of the candidate genes with the strongest effect on dilp expression, Homothorax, a transcription factor known for its role in eye development. We found that Homothorax and its binding partner Extradenticle are involved in regulating dilp2, -3 and -5 expression and that genetic depletion of both TFs shows phenotypes associated with reduced insulin signalling. Furthermore, we provide evidence that other transcription factors involved in eye development are also functional in the IPCs. In conclusion, we showed that this expression level-based GWAS approach identified genetic regulators implicated in IPC function and dilp expression.
果蝇胰岛素分泌细胞(IPCs)是果蝇胰岛素样肽或 dilps 的主要产生部位,它们在调节生长、发育、繁殖、寿命和代谢方面发挥着关键作用。为了更好地理解在 IPCs 中活跃的信号通路和转录网络,我们查询了超过 180 条高度近交系果蝇品系的公开转录组数据,以获取 dilp 表达情况,并将 dilp 表达作为全基因组关联研究(GWAS)的输入。这导致鉴定出 125 个基因中的变体与 dilp 表达的变异相关。我们使用基于 RNAi 的方法测试了这些基因中 57 个基因在 IPCs 中的功能。我们发现,IPC 特异性耗尽大多数基因会导致一个或多个 dilp 的表达差异。然后,我们进一步研究了候选基因中对 dilp 表达影响最强的一个基因,即 Homothorax,它是一种已知在眼睛发育中起作用的转录因子。我们发现 Homothorax 和其结合伴侣 Extradenticle 参与调节 dilp2、-3 和 -5 的表达,并且这两种 TF 的遗传耗竭都表现出与胰岛素信号降低相关的表型。此外,我们提供了证据表明,参与眼睛发育的其他转录因子在 IPCs 中也具有功能。总之,我们表明,这种基于表达水平的 GWAS 方法鉴定出了与 IPC 功能和 dilp 表达相关的遗传调节剂。