• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基因表达重排表示生物状态的变化。

Gene expression rearrangements denoting changes in the biological state.

机构信息

University of Electronic Science and Technology, 610051, Chengdu, People's Republic of China.

Institute of Cybernetics, Mathematics and Physics, 10400, Havana, Cuba.

出版信息

Sci Rep. 2021 Apr 19;11(1):8470. doi: 10.1038/s41598-021-87764-0.

DOI:10.1038/s41598-021-87764-0
PMID:33875699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8055689/
Abstract

In many situations, the gene expression signature is a unique marker of the biological state. We study the modification of the gene expression distribution function when the biological state of a system experiences a change. This change may be the result of a selective pressure, as in the Long Term Evolution Experiment with E. Coli populations, or the progression to Alzheimer disease in aged brains, or the progression from a normal tissue to the cancer state. The first two cases seem to belong to a class of transitions, where the initial and final states are relatively close to each other, and the distribution function for the differential expressions is short ranged, with a tail of only a few dozens of strongly varying genes. In the latter case, cancer, the initial and final states are far apart and separated by a low-fitness barrier. The distribution function shows a very heavy tail, with thousands of silenced and over-expressed genes. We characterize the biological states by means of their principal component representations, and the expression distribution functions by their maximal and minimal differential expression values and the exponents of the Pareto laws describing the tails.

摘要

在许多情况下,基因表达特征是生物状态的独特标记。我们研究当系统的生物状态发生变化时,基因表达分布函数的变化。这种变化可能是选择压力的结果,如在大肠杆菌种群的长期进化实验中,或在老年大脑中阿尔茨海默病的进展中,或在正常组织向癌症状态的进展中。前两种情况似乎属于一类跃迁,其中初始状态和最终状态彼此相对接近,差异表达的分布函数具有短程性,只有少数几十个强烈变化的基因。在后一种情况下,即癌症中,初始状态和最终状态相距甚远,中间隔着一个低适应度的障碍。分布函数显示出非常重的尾部,有数千个沉默和过度表达的基因。我们通过主成分表示来描述生物状态,通过最大和最小差异表达值以及描述尾部的帕累托定律的指数来描述表达分布函数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/856d3467e47f/41598_2021_87764_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/92fc6ab3a00e/41598_2021_87764_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/34505099af51/41598_2021_87764_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/b83eb2d9c03e/41598_2021_87764_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/5490f1ea0911/41598_2021_87764_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/856d3467e47f/41598_2021_87764_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/92fc6ab3a00e/41598_2021_87764_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/34505099af51/41598_2021_87764_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/b83eb2d9c03e/41598_2021_87764_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/5490f1ea0911/41598_2021_87764_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/8055689/856d3467e47f/41598_2021_87764_Fig5_HTML.jpg

相似文献

1
Gene expression rearrangements denoting changes in the biological state.基因表达重排表示生物状态的变化。
Sci Rep. 2021 Apr 19;11(1):8470. doi: 10.1038/s41598-021-87764-0.
2
Brain transcriptome analysis reveals subtle effects on mitochondrial function and iron homeostasis of mutations in the SORL1 gene implicated in early onset familial Alzheimer's disease.脑转录组分析揭示了 SORL1 基因突变对线粒体功能和铁平衡的微妙影响,该基因突变与早发性家族性阿尔茨海默病有关。
Mol Brain. 2020 Oct 19;13(1):142. doi: 10.1186/s13041-020-00681-7.
3
Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease.对19个脑区的综合网络分析确定了阿尔茨海默病选择性区域易损性背后的分子特征和网络。
Genome Med. 2016 Nov 1;8(1):104. doi: 10.1186/s13073-016-0355-3.
4
Large chromosomal rearrangements during a long-term evolution experiment with Escherichia coli.在一项针对大肠杆菌的长期进化实验中出现的大型染色体重排。
mBio. 2014 Sep 9;5(5):e01377-14. doi: 10.1128/mBio.01377-14.
5
Mitochondrial DNA Rearrangement Spectrum in Brain Tissue of Alzheimer's Disease: Analysis of 13 Cases.阿尔茨海默病脑组织中的线粒体DNA重排谱:13例分析
PLoS One. 2016 Jun 14;11(6):e0154582. doi: 10.1371/journal.pone.0154582. eCollection 2016.
6
Neuronal gene expression in non-demented individuals with intermediate Alzheimer's Disease neuropathology.非痴呆的阿尔茨海默病病理学中间阶段个体的神经元基因表达。
Neurobiol Aging. 2010 Apr;31(4):549-66. doi: 10.1016/j.neurobiolaging.2008.05.013. Epub 2008 Jun 24.
7
Single cell gene expression profiling in Alzheimer's disease.阿尔茨海默病中的单细胞基因表达谱分析。
NeuroRx. 2006 Jul;3(3):302-18. doi: 10.1016/j.nurx.2006.05.007.
8
Whole transcriptome sequencing reveals gene expression and splicing differences in brain regions affected by Alzheimer's disease.全转录组测序揭示了受阿尔茨海默病影响的大脑区域的基因表达和剪接差异。
PLoS One. 2011 Jan 21;6(1):e16266. doi: 10.1371/journal.pone.0016266.
9
Altered neuronal gene expression in brain regions differentially affected by Alzheimer's disease: a reference data set.阿尔茨海默病不同程度影响的脑区中神经元基因表达的改变:一个参考数据集
Physiol Genomics. 2008 Apr 22;33(2):240-56. doi: 10.1152/physiolgenomics.00242.2007. Epub 2008 Feb 12.
10
Identification of expression patterns in the progression of disease stages by integration of transcriptomic data.通过整合转录组数据识别疾病阶段进展中的表达模式。
BMC Bioinformatics. 2016 Nov 22;17(Suppl 15):432. doi: 10.1186/s12859-016-1290-4.

引用本文的文献

1
A bird's eye view to the homeostatic, Alzheimer and Glioblastoma attractors.对稳态、阿尔茨海默病和胶质母细胞瘤吸引子的鸟瞰。
Heliyon. 2025 Feb 4;11(4):e42445. doi: 10.1016/j.heliyon.2025.e42445. eCollection 2025 Feb 28.
2
On the gene expression landscape of cancer.癌症的基因表达图谱。
PLoS One. 2023 Feb 21;18(2):e0277786. doi: 10.1371/journal.pone.0277786. eCollection 2023.
3
Estimating the number of available states for normal and tumor tissues in gene expression space.估计基因表达空间中正常组织和肿瘤组织的可用状态数量。

本文引用的文献

1
On the gene expression landscape of cancer.癌症的基因表达图谱。
PLoS One. 2023 Feb 21;18(2):e0277786. doi: 10.1371/journal.pone.0277786. eCollection 2023.
2
Estimating the number of available states for normal and tumor tissues in gene expression space.估计基因表达空间中正常组织和肿瘤组织的可用状态数量。
Biophys Rep (N Y). 2022 Mar 30;2(2):100053. doi: 10.1016/j.bpr.2022.100053. eCollection 2022 Jun 8.
3
Mutations as Levy flights.突变作为 Levy 飞行。
Biophys Rep (N Y). 2022 Mar 30;2(2):100053. doi: 10.1016/j.bpr.2022.100053. eCollection 2022 Jun 8.
4
A one-dimensional parameter-free model for carcinogenesis in gene expression space.在基因表达空间中致癌作用的一维无参数模型。
Sci Rep. 2022 Mar 19;12(1):4748. doi: 10.1038/s41598-022-08502-8.
Sci Rep. 2021 May 10;11(1):9889. doi: 10.1038/s41598-021-88012-1.
4
Single-cell transcriptome profiling of an adult human cell atlas of 15 major organs.人类 15 大主要器官单细胞转录组图谱绘制。
Genome Biol. 2020 Dec 7;21(1):294. doi: 10.1186/s13059-020-02210-0.
5
Construction of a human cell landscape at single-cell level.在单细胞水平构建人类细胞图谱。
Nature. 2020 May;581(7808):303-309. doi: 10.1038/s41586-020-2157-4. Epub 2020 Mar 25.
6
Revisiting the tumorigenesis timeline with a data-driven generative model.基于数据驱动的生成模型重探肿瘤发生时间线。
Proc Natl Acad Sci U S A. 2020 Jan 14;117(2):857-864. doi: 10.1073/pnas.1914589117. Epub 2019 Dec 27.
7
Epigenetic dysregulation of enhancers in neurons is associated with Alzheimer's disease pathology and cognitive symptoms.神经元中增强子的表观遗传失调与阿尔茨海默病病理和认知症状有关。
Nat Commun. 2019 May 21;10(1):2246. doi: 10.1038/s41467-019-10101-7.
8
Neuropathological and transcriptomic characteristics of the aged brain.老年人大脑的神经病理学和转录组学特征。
Elife. 2017 Nov 9;6:e31126. doi: 10.7554/eLife.31126.
9
Stem cell divisions, somatic mutations, cancer etiology, and cancer prevention.干细胞分裂、体细胞突变、癌症病因学与癌症预防。
Science. 2017 Mar 24;355(6331):1330-1334. doi: 10.1126/science.aaf9011.
10
Diagnosis of cancer as an emergency: a critical review of current evidence.将癌症诊断视为紧急情况:对当前证据的批判性回顾。
Nat Rev Clin Oncol. 2017 Jan;14(1):45-56. doi: 10.1038/nrclinonc.2016.155. Epub 2016 Oct 11.