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DNA Microarray Analysis of the Mouse Adrenal Gland for the Detection of Hypothermia Biomarkers: Potential Usefulness for Forensic Investigation

机译:小鼠肾上腺的DNA芯片分析以检测体温过低的生物标志物:法医调查的潜在用途

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摘要

We analyzed the adrenal gland transcriptome of mice killed by hypothermia using DNA microarray technology. A total of 4051 significantly expressed genes were identified; 2015 genes were upregulated and 2036 were downregulated. The FBJ osteosarcoma oncogene was the most upregulated, whereas stearoyl coenzyme A desaturase 3 was the most downregulated. Validation by quantitative polymerase chain reaction revealed that results obtained by both methods were consistent. In the gene set analysis, significant variations were found in nine pathways, and we suggest that transforming growth factor β and tumor necrosis factor α would be involved in the pathogenesis of hypothermia. Gene functional category analysis demonstrated the most overexpressed categories in upregulated and downregulated genes were cellular process in biological process, binding in molecular function, and cell and cell part in cellular component. The present study demonstrated acute adrenal responses in hypothermia, and we suggest that understanding adrenal mRNA expression would be useful for hypothermia diagnosis. Furthermore, the present microarray data may also facilitate development of immunohistochemical analysis of human cases. In forensic practice, the combination of macroscopic and microscopic observations with molecular biological analyses would be conducive to more accurate diagnosis of hypothermia. Although this study is aimed at forensic practice, the present data regarding more than 20,000 genes of the adrenal gland would be beneficial to inform future clinical hypothermia research. From the viewpoint of adrenal gene activity, they could contribute to elucidating the pathophysiology of hypothermia.
机译:我们使用DNA芯片技术分析了低温致死小鼠的肾上腺转录组。总共鉴定了4051个显着表达的基因; 2015年基因被上调,而2036年被下调。 FBJ骨肉瘤癌基因被上调最多,而硬脂酰辅酶A去饱和酶3被下调最多。通过定量聚合酶链反应的验证显示,通过两种方法获得的结果是一致的。在基因组分析中,在九种途径中发现了显着差异,我们建议转化生长因子β和肿瘤坏死因子α参与体温过低的发病机理。基因功能类别分析表明,在上调和下调的基因中表达最多的类别是生物过程中的细胞过程,分子功能中的结合以及细胞成分中的细胞和细胞部分。本研究显示了低温时的急性肾上腺反应,我们建议了解肾上腺mRNA的表达将有助于低温诊断。此外,当前的微阵列数据还可以促进人类病例的免疫组织化学分析的发展。在法医实践中,将宏观和微观观察与分子生物学分析相结合将有助于更准确地诊断体温过低。尽管这项研究的目的是法医实践,但有关肾上腺20,000多个基因的当前数据将有益于为未来的临床体温过低研究提供信息。从肾上腺基因活性的观点来看,它们可能有助于阐明体温过低的病理生理。

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