RNA-Seq 数据分析显示了本体发生如何定义衰老。

IF 3.3 Q2 GERIATRICS & GERONTOLOGY
Frontiers in aging Pub Date : 2023-03-14 eCollection Date: 2023-01-01 DOI:10.3389/fragi.2023.1143334
Lev Salnikov, Saveli Goldberg, Heena Rijhwani, Yuran Shi, Eugene Pinsky
{"title":"RNA-Seq 数据分析显示了本体发生如何定义衰老。","authors":"Lev Salnikov, Saveli Goldberg, Heena Rijhwani, Yuran Shi, Eugene Pinsky","doi":"10.3389/fragi.2023.1143334","DOIUrl":null,"url":null,"abstract":"<p><p>This paper presents a global statistical analysis of the RNA-Seq results of the entire <i>Mus musculus</i> genome. We explain aging by a gradual redistribution of limited resources between two major tasks of the organism: its self-sustenance based on the function of the housekeeping gene group (HG) and functional differentiation provided by the integrative gene group (IntG). All known disorders associated with aging are the result of a deficiency in the repair processes provided by the cellular infrastructure. Understanding exactly how this deficiency arises is our primary goal. Analysis of RNA production data of 35,630 genes, from which 5,101 were identified as HG genes, showed that RNA production levels in the HG and IntG genes had statistically significant differences (<i>p</i>-value <0.0001) throughout the entire observation period. In the reproductive period of life, which has the lowest actual mortality risk for <i>Mus musculus</i>, changes in the age dynamics of RNA production occur. The statistically significant dynamics of the decrease of RNA production in the HG group in contrast to the IntG group was determined (<i>p</i>-value = 0.0045). The trend toward significant shift in the HG/IntG ratio occurs after the end of the reproductive period, coinciding with the beginning of the mortality rate increase in <i>Mus musculus</i> indirectly supports our hypothesis. The results demonstrate a different orientation of the impact of ontogenesis regulatory mechanisms on the groups of genes representing cell infrastructures and their organismal functions, making the chosen direction promising for further research and understanding the mechanisms of aging.</p>","PeriodicalId":73061,"journal":{"name":"Frontiers in aging","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2023-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046809/pdf/","citationCount":"0","resultStr":"{\"title\":\"The RNA-Seq data analysis shows how the ontogenesis defines aging.\",\"authors\":\"Lev Salnikov, Saveli Goldberg, Heena Rijhwani, Yuran Shi, Eugene Pinsky\",\"doi\":\"10.3389/fragi.2023.1143334\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This paper presents a global statistical analysis of the RNA-Seq results of the entire <i>Mus musculus</i> genome. We explain aging by a gradual redistribution of limited resources between two major tasks of the organism: its self-sustenance based on the function of the housekeeping gene group (HG) and functional differentiation provided by the integrative gene group (IntG). All known disorders associated with aging are the result of a deficiency in the repair processes provided by the cellular infrastructure. Understanding exactly how this deficiency arises is our primary goal. Analysis of RNA production data of 35,630 genes, from which 5,101 were identified as HG genes, showed that RNA production levels in the HG and IntG genes had statistically significant differences (<i>p</i>-value <0.0001) throughout the entire observation period. In the reproductive period of life, which has the lowest actual mortality risk for <i>Mus musculus</i>, changes in the age dynamics of RNA production occur. The statistically significant dynamics of the decrease of RNA production in the HG group in contrast to the IntG group was determined (<i>p</i>-value = 0.0045). The trend toward significant shift in the HG/IntG ratio occurs after the end of the reproductive period, coinciding with the beginning of the mortality rate increase in <i>Mus musculus</i> indirectly supports our hypothesis. The results demonstrate a different orientation of the impact of ontogenesis regulatory mechanisms on the groups of genes representing cell infrastructures and their organismal functions, making the chosen direction promising for further research and understanding the mechanisms of aging.</p>\",\"PeriodicalId\":73061,\"journal\":{\"name\":\"Frontiers in aging\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2023-03-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046809/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in aging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3389/fragi.2023.1143334\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"GERIATRICS & GERONTOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in aging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fragi.2023.1143334","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

本文对整个麝香鹿基因组的 RNA-Seq 结果进行了全局统计分析。我们对衰老的解释是,有限的资源在生物体的两大任务之间逐渐重新分配:基于看家基因组(HG)功能的自我维持和整合基因组(IntG)提供的功能分化。所有已知的与衰老相关的疾病都是细胞基础设施提供的修复过程不足的结果。了解这种缺陷是如何产生的是我们的首要目标。对 35,630 个基因(其中 5,101 个被确定为 HG 基因)的 RNA 生产数据进行分析后发现,HG 基因和 IntG 基因的 RNA 生产水平在统计学上有显著差异(P 值 麝香草,RNA 生产的年龄动态发生变化。与 IntG 组相比,HG 组 RNA 产量的下降动态具有统计学意义(p 值 = 0.0045)。HG/IntG 比率在生殖期结束后出现明显变化的趋势,与麝的死亡率开始上升相吻合,间接支持了我们的假设。研究结果表明,本体发生调控机制对代表细胞基础结构及其机体功能的基因组的影响具有不同的方向性,因此所选择的方向对进一步研究和理解衰老机制具有良好的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The RNA-Seq data analysis shows how the ontogenesis defines aging.

The RNA-Seq data analysis shows how the ontogenesis defines aging.

The RNA-Seq data analysis shows how the ontogenesis defines aging.

The RNA-Seq data analysis shows how the ontogenesis defines aging.

This paper presents a global statistical analysis of the RNA-Seq results of the entire Mus musculus genome. We explain aging by a gradual redistribution of limited resources between two major tasks of the organism: its self-sustenance based on the function of the housekeeping gene group (HG) and functional differentiation provided by the integrative gene group (IntG). All known disorders associated with aging are the result of a deficiency in the repair processes provided by the cellular infrastructure. Understanding exactly how this deficiency arises is our primary goal. Analysis of RNA production data of 35,630 genes, from which 5,101 were identified as HG genes, showed that RNA production levels in the HG and IntG genes had statistically significant differences (p-value <0.0001) throughout the entire observation period. In the reproductive period of life, which has the lowest actual mortality risk for Mus musculus, changes in the age dynamics of RNA production occur. The statistically significant dynamics of the decrease of RNA production in the HG group in contrast to the IntG group was determined (p-value = 0.0045). The trend toward significant shift in the HG/IntG ratio occurs after the end of the reproductive period, coinciding with the beginning of the mortality rate increase in Mus musculus indirectly supports our hypothesis. The results demonstrate a different orientation of the impact of ontogenesis regulatory mechanisms on the groups of genes representing cell infrastructures and their organismal functions, making the chosen direction promising for further research and understanding the mechanisms of aging.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.00
自引率
0.00%
发文量
0
审稿时长
13 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信