Carausius morosus (Phasmatodea) Homologues of Human Genes with Elevated Expression in the Colon

M. Shelomi
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Abstract

Background: Preliminary testing of novel drugs for colorectal conditions must be performed on animal models, with invertebratemodels desirable for practical reasons. The insect excretory organs, the Malpighian tubules, have been cited as models for humanrenal disease research because they differentially express several genes homologous to those differentially expressed in humankidneys. Their role in excretion and homeostasis suggests that they could be models for human colorectal disease. The insect Carausiusmorosus (Phasmatodea) has been a model organism for decades. Regarding its potential use as a colorectal disease model,it has an advantage over other insects in that excretion in Phasmatodea is split between two organs: Malpighian tubules and thePhasmatodea-specific “appendices of the midgut”.Objectives: To find homologues of human colon genes expressed in the excretory tissues of C. morosus for potential use in drugtesting and other experiments requiring an animal model.Methods: Pre-existing transcriptomics data for the excretory system of the C. morosus were examined to find genes homologous tothose known to have elevated expression in the human colon. This was done with the goal of possibly determining the excretorytissues in which they are differentially expressed.Results: Exactly sixty transcripts from the excretory system transcriptome of C. morosus showed high sequence homology withhuman colon-specific genes, with a minimum e-value of 1e-50. Examples include solute carriers, myosin, bestrophin, carbonic anhydrase,and nitric oxide synthase. Several genes were identified with prognostic value for renal, pancreatic, endometrial, liver, skin,and urothelial cancers.Conclusions: C. morosus can be used as model insect for human medical research applications, including colorectal drug testing.
人类结肠中表达升高基因的同源性研究
背景:治疗结直肠疾病的新药的初步试验必须在动物模型上进行,由于实际原因,无脊椎动物模型是可取的。昆虫的排泄器官马氏小管被引用为人类肾脏疾病研究的模型,因为它们表达的几个基因与人类肾脏中表达的基因存在差异。它们在排泄和体内平衡中的作用表明它们可能是人类结直肠疾病的模型。昆虫Carausiusmorosus (Phasmatodea)几十年来一直是一种模式生物。考虑到它作为结直肠疾病模型的潜在用途,它比其他昆虫有一个优势,即Phasmatodea的排泄在两个器官之间分裂:Malpighian小管和Phasmatodea特有的“中肠阑尾”。目的:寻找在morosus C.排泄组织中表达的人类结肠基因的同源物,用于药物测试和其他需要动物模型的实验。方法:对morosus C.排泄系统已有的转录组学数据进行检查,寻找与已知在人类结肠中表达升高的基因同源的基因。这样做的目的可能是确定它们在哪些排泄组织中有差异表达。结果:morosus排泄系统转录组中有60个转录本与人类结肠特异性基因具有高度同源性,其e值最小为1e-50。例子包括溶质载体、肌球蛋白、肌球蛋白、碳酸酐酶和一氧化氮合酶。几个基因被确定为肾脏、胰腺、子宫内膜、肝脏、皮肤和尿路上皮癌的预后价值。结论:morosus可作为人体医学研究的模式昆虫,包括结肠直肠药物试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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