Department of Biological Sciences, Delaware State University, Dover, DE, USA.
Forensic Science Program, Physical Sciences Department, Alabama State University, Montgomery, AL, USA.
Gene. 2020 Mar 20;731:144349. doi: 10.1016/j.gene.2020.144349. Epub 2020 Jan 11.
Gene expression is the process by which DNA is decoded to produce a functional transcript. The collection of all transcripts is referred to as the transcriptome and has extensively been used to evaluate differentially expressed genes in a certain cell or tissue type. In response to internal or external stimuli, the transcriptome is greatly regulated by epigenetic changes. Many studies have elucidated that antemortem gene expression (transcriptome) may be linked to an array of disease etiologies as well as potential targets for drug discovery; on the other hand, a number of studies have utilized postmortem gene expression (thanatotranscriptome) patterns to determine cause and time of death. The "transcriptome after death" involves the study of mRNA transcripts occurring in human tissues after death (thanatos, Greek for death). While antemortem gene expression can provide a wide range of important information about the host, the determination of the communication of genes after a human dies has recently been explored. After death a plethora of genes are regulated via activation versus repression as well as diverse regulatory factors such as the absence or presence of stimulated feedback. Even postmortem transcriptional regulation contains many more cellular constituents and is massively more complicated. The rates of degradation of mRNA transcripts vary depending on the types of postmortem tissues and their combinatorial gene expression signatures. mRNA molecules have been shown to persist for extended time frames; nevertheless, they are highly susceptible to degradation, with half-lives of selected mRNAs varying between minutes to weeks for specifically induced genes. Furthermore, postmortem genetic studies may be used to improve organ transplantation techniques. This review is the first of its kind to fully explore both gene expression and mRNA stability after death and the trove of information that can be provided about phenotypical characteristics of specific genes postmortem.
基因表达是 DNA 被解码以产生功能性转录本的过程。所有转录本的集合被称为转录组,广泛用于评估特定细胞或组织类型中差异表达的基因。转录组受到表观遗传变化的极大调节,以响应内部或外部刺激。许多研究已经阐明,生前基因表达(转录组)可能与一系列疾病病因以及药物发现的潜在靶点有关;另一方面,许多研究利用死后基因表达(尸检转录组)模式来确定死因和死亡时间。“死后转录组”涉及研究人类组织在死后发生的 mRNA 转录本(thanatos,希腊语为死亡)。虽然生前基因表达可以提供宿主的广泛重要信息,但人类死后基因的通讯测定最近已被探索。死亡后,大量基因通过激活与抑制以及各种调节因子(如刺激反馈的有无)进行调节。即使是死后转录调控也包含更多的细胞成分,并且更加复杂。mRNA 转录本的降解率取决于死后组织的类型及其组合基因表达特征。mRNA 分子已被证明可以持续很长时间;然而,它们极易降解,特定诱导基因的选定 mRNA 的半衰期在几分钟到几周之间变化。此外,死后遗传研究可用于改进器官移植技术。这是首次全面探索死后基因表达和 mRNA 稳定性以及死后特定基因表型特征可提供的大量信息的综述。