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Microarray analysis of miRNAs during hindgut development in rat embryos with ethylenethiourea-induced anorectal malformations

机译:乙烯硫脲诱导的肛门直肠畸形大鼠胚胎后肠发育过程中miRNA的微阵列分析

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摘要

Anorectal malformations (ARMs) are one of the most common congenital malformations of the digestive tract; however, the pathogenesis of this disease remains to be fully elucidated. MicroRNAs (miRNAs) are important in gastrointestinal development and may be involved in the pathogenesis of ARMs. The present study aimed to profile miRNAs and examine their potential functions in rats with ethylenethiourea (ETU)-induced ARMs. Pregnant Wistar rats (n=36) were divided randomly into ETU-treated and control groups. The rats in the ETU-treated group were gavage-fed 1% ETU (125 mg/kg) on gestational day 10 (GD10), whereas the control group rats received a corresponding dose of saline. Embryos were harvested by cesarean section on GD14, GD15 and GD16. Hindgut tissue was isolated from the fetuses for RNA extraction and microarray analysis, followed by bioinformatics analysis and reverse transcription-quantitative polymerase chain reaction (RT-qPCR) validation. Overall, 38 miRNAs were differentially expressed (all upregulated) on GD14, 49 (32 upregulated and 17 downregulated) on GD15, and 42 (all upregulated) on GD16 in the ARM group compared with the normal group. The top 18 miRNAs with |log2(fold change)| >4.25 were selected for further bioinformatics analysis. Among these miRNAs, five were differentially expressed at two time-points and were involved in ARM-associated signaling pathways. The RT-qPCR analysis revealed that three miRNA (miR), miR-125b-2-3p, miR-92a-2-5p and miR-99a-5p, were significantly differentially expressed in rats with ARMs compared with the normal group. In conclusion, the results suggested that the differential expression of miR-125b-2-3p, miR-92a-2-5p and miR-99a-5p during key time-points of anorectal formation in rats may have functions in the pathogenesis of ARM.
机译:肛门直肠畸形(ARMs)是消化道最常见的先天性畸形之一。然而,该病的发病机理仍有待充分阐明。 MicroRNA(miRNA)在胃肠道发育中很重要,可能与ARM的发病机制有关。本研究旨在分析miRNA并检查其在亚乙基硫脲(ETU)诱导的ARM大鼠中的潜在功能。将怀Wistar大鼠(n = 36)随机分为ETU治疗组和对照组。在妊娠第10天(GD10),以ETU治疗组的大鼠灌胃饲喂1%ETU(125 mg / kg),而对照组大鼠则接受相应剂量的生理盐水。通过剖腹产在GD14,GD15和GD16上收获胚胎。从胎儿中分离出后肠组织用于RNA提取和微阵列分析,然后进行生物信息学分析和逆转录定量聚合酶链反应(RT-qPCR)验证。总体而言,与正常组相比,ARM组在GD14上差异表达(全部上调)38个miRNA,在GD15上差异表达49个(全部上调32个,下调17个),在GD16上差异表达42个(全部上调)。 | log2(倍数变化)|的前18个miRNA选择> 4.25进行进一步的生物信息学分析。在这些miRNA中,有五个在两个时间点差异表达,并参与ARM相关的信号通路。 RT-qPCR分析显示,与正常组相比,在具有ARM的大鼠中三种miRNA(miR),miR-125b-2-3p,miR-92a-2-5p和miR-99a-5p显着差异表达。总之,结果表明在大鼠肛肠形成关键时间点,miR-125b-2-3p,miR-92a-2-5p和miR-99a-5p的差异表达可能与ARM的发病机制有关。 。

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