McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
BMC Genomics. 2012 Jan 17;13:26. doi: 10.1186/1471-2164-13-26.
Gene expression studies can be used to help identify disease-associated genes by comparing the levels of expressed transcripts between cases and controls, and to identify functional genetic variants (expression quantitative loci or eQTLs) by comparing expression levels between individuals with different genotypes. While many of these studies are performed in blood or lymphoblastoid cell lines due to tissue accessibility, the relevance of expression differences in tissues that are not the primary site of disease is unclear. Further, many eQTLs are tissue specific. Thus, there is a clear and compelling need to conduct gene expression studies in tissues that are specifically relevant to the disease of interest. One major technical concern about using autopsy-derived tissue is how representative it is of physiologic conditions, given the effect of postmortem interval on tissue degradation.
In this study, we monitored the gene expression of 13 tissue samples harvested from a rapid autopsy heart (non-failed heart) and 7 from a cardiac explant (failed heart) through 24 hours of autolysis. The 24 hour autopsy simulation was designed to reflect a typical autopsy scenario where a body may begin cooling to ambient temperature for ~12 hours, before transportation and storage in a refrigerated room in a morgue. In addition, we also simulated a scenario wherein the body was left at room temperature for up to 24 hours before being found. A small fraction (< 2.5%) of genes showed fluctuations in expression over the 24 hr period and largely belong to immune and signal response and energy metabolism-related processes. Global expression analysis suggests that RNA expression is reproducible over 24 hours of autolysis with 95% genes showing < 1.2 fold change. Comparing the rapid autopsy to the failed heart identified 480 differentially expressed genes, including several types of collagens, lumican (LUM), natriuretic peptide A (NPPA) and connective tissue growth factor (CTGF), which allows for the clear separation between failing and non-failing heart based on gene expression profiles.
Our results demonstrate that RNA from autopsy-derived tissue, even up to 24 hours of autolysis, can be used to identify biologically relevant expression pattern differences, thus serving as a practical source for gene expression experiments.
通过比较病例和对照之间表达转录本的水平,基因表达研究可用于帮助识别疾病相关基因,并通过比较不同基因型个体之间的表达水平来识别功能遗传变异(表达定量基因座或 eQTL)。由于组织可及性,许多此类研究是在血液或淋巴母细胞系中进行的,但在非疾病主要部位的组织中表达差异的相关性尚不清楚。此外,许多 eQTL 是组织特异性的。因此,迫切需要在与感兴趣的疾病特别相关的组织中进行基因表达研究。使用尸检组织的一个主要技术问题是,考虑到死后间隔时间对组织降解的影响,它在多大程度上代表生理条件。
在这项研究中,我们通过 24 小时自溶监测了 13 个快速尸检心脏(未衰竭心脏)和 7 个心脏外植体(衰竭心脏)组织样本的基因表达。24 小时尸检模拟旨在反映典型的尸检情况,即尸体可能开始冷却到环境温度约 12 小时,然后在停尸房的冷藏室中运输和储存。此外,我们还模拟了在发现尸体之前,将其放置在室温下长达 24 小时的情况。在 24 小时内,只有一小部分(<2.5%)基因的表达出现波动,主要属于免疫和信号反应以及能量代谢相关过程。全局表达分析表明,在 24 小时自溶过程中,RNA 表达具有重现性,95%的基因显示<1.2 倍变化。将快速尸检与衰竭心脏进行比较,确定了 480 个差异表达基因,包括几种类型的胶原蛋白、光氨酸(LUM)、利尿钠肽 A(NPPA)和结缔组织生长因子(CTGF),根据基因表达谱可以清楚地区分衰竭和非衰竭心脏。
我们的研究结果表明,即使在自溶 24 小时后,尸检组织的 RNA 仍可用于识别具有生物学意义的表达模式差异,因此可作为基因表达实验的实用来源。