Microtubule-Rab5 mutual-influential system screening based on gene-regulatory networks map in Rab5 RNAi eye-degeneration model

IF 4.4 2区 生物学 Q2 CELL BIOLOGY Cellular signalling Pub Date : 2024-12-02 DOI:10.1016/j.cellsig.2024.111544
Yuyu Nan , Jingjing Lin , Zaiwa Wei , Yufeng Yang , Qinghua Li
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Abstract

Rabs are involved in neuronal development and protrusion formation. Existing studies support the notion that manipulation or mutation of Rab genes could lead to functional changes in neurons. However, whether Rabs gene-manipulation induced Drosophila eye-degeneration remains unknown. By down-regulating Rab5, but not Rab7, we first constructed a compound eye injury model in Drosophila. As the distribution, content, and even maturation of Rab5-positive endosomes are influenced by cytoskeletal proteins, like actin or tubulin-related proteins, the existence of a bidirectional regulatory relationship between Rab5 and the cytoskeleton remains unclear and worth researching. Through complete transcriptome sequencing combined immunofluorescence testing, we confirmed that down-regulation of Rab5 affected the increase of α-Tub84B (alternatively named TubA84B) but not γ-tubulin. Based on Weighted Gene Co-Expression Network Analysis (WGCNA) and multi-tissue screening verification, this study proposes that the apoptosis-related factors–Rab5–TubA84B have conserved regulatory functions with cooperative expression. Gene manipulation confirmed that apoptotic factors, especially rpr, strongly regulate Rab5, and may ultimately influence microtubule structure through complex routes, including the Rab5 variance and the intracellular configuration ratio of α-Tubulin to Glyceraldehyde-3-phosphate dehydrogenase.
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Rab5 RNAi眼变性模型中基于基因调控网络图谱的微管-Rab5互影响系统筛选
Rabs参与神经元的发育和突起的形成。现有的研究支持这样一种观点,即操纵或突变Rab基因可能导致神经元的功能改变。然而,Rabs基因操作是否导致果蝇眼睛变性仍然未知。通过下调Rab5而不下调Rab7,我们首次构建了果蝇复眼损伤模型。由于Rab5阳性核内体的分布、含量甚至成熟都受到细胞骨架蛋白(如肌动蛋白或微管蛋白相关蛋白)的影响,Rab5与细胞骨架之间是否存在双向调节关系尚不清楚,值得进一步研究。通过全转录组测序结合免疫荧光检测,我们证实Rab5的下调影响α-Tub84B(也称为TubA84B)的升高,但不影响γ-微管蛋白的升高。基于加权基因共表达网络分析(Weighted Gene Co-Expression Network Analysis, WGCNA)和多组织筛选验证,本研究提出凋亡相关因子- rab5 - tuba84b具有协同表达的保守调控功能。基因操作证实,凋亡因子,尤其是rpr,强烈调节Rab5,并可能最终通过复杂的途径影响微管结构,包括Rab5变异和α-微管蛋白与甘油醛-3-磷酸脱氢酶的胞内构型比。
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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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