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追踪生物体死亡后基因转录本的动态变化。

Tracing the dynamics of gene transcripts after organismal death.

作者信息

Pozhitkov Alex E, Neme Rafik, Domazet-Lošo Tomislav, Leroux Brian G, Soni Shivani, Tautz Diethard, Noble Peter A

机构信息

Department of Oral Health Sciences, University of Washington, PO Box 357444, Seattle, WA 98195, USA.

Max Planck Institute for Evolutionary Biology, August-Thienemann-Strasse 2, 24306 Ploen, Germany.

出版信息

Open Biol. 2017 Jan;7(1). doi: 10.1098/rsob.160267.

Abstract

In life, genetic and epigenetic networks precisely coordinate the expression of genes-but in death, it is not known if gene expression diminishes gradually or abruptly stops or if specific genes and pathways are involved. We studied this by identifying mRNA transcripts that apparently increase in relative abundance after death, assessing their functions, and comparing their abundance profiles through postmortem time in two species, mouse and zebrafish. We found mRNA transcript profiles of 1063 genes became significantly more abundant after death of healthy adult animals in a time series spanning up to 96 h postmortem. Ordination plots revealed non-random patterns in the profiles by time. While most of these transcript levels increased within 0.5 h postmortem, some increased only at 24 and 48 h postmortem. Functional characterization of the most abundant transcripts revealed the following categories: stress, immunity, inflammation, apoptosis, transport, development, epigenetic regulation and cancer. The data suggest a step-wise shutdown occurs in organismal death that is manifested by the apparent increase of certain transcripts with various abundance maxima and durations.

摘要

在生命过程中,遗传和表观遗传网络精确地协调基因表达,但在死亡过程中,基因表达是逐渐减少、突然停止,还是涉及特定基因和信号通路,目前尚不清楚。我们通过鉴定死后相对丰度明显增加的mRNA转录本、评估其功能,并比较小鼠和斑马鱼这两个物种死后不同时间的丰度谱,对此进行了研究。我们发现,在长达96小时的死后时间序列中,健康成年动物死亡后,1063个基因的mRNA转录本谱变得明显更加丰富。排序图显示这些谱随时间呈现非随机模式。虽然这些转录本水平大多在死后0.5小时内增加,但有些仅在死后24小时和48小时增加。对最丰富转录本的功能表征揭示了以下类别:应激、免疫、炎症、凋亡、转运、发育、表观遗传调控和癌症。数据表明,机体死亡时会发生逐步关闭,表现为某些转录本明显增加,具有不同的丰度最大值和持续时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978a/5303275/7272601961df/rsob-7-160267-g1.jpg

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