• 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

探索发育性神经视网膜中二硫键断裂的起源和生理意义。

Exploring the Origin and Physiological Significance of DNA Double Strand Breaks in the Developing Neuroretina.

机构信息

3D Lab (Development, Differentiation and Degeneration), Centro de Investigaciones Biológicas Margarita Salas, CSIC, Ramiro de Maeztu 9, 28040 Madrid, Spain.

出版信息

Int J Mol Sci. 2022 Jun 9;23(12):6449. doi: 10.3390/ijms23126449.

DOI:10.3390/ijms23126449
PMID:35742893
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9224223/
Abstract

Genetic mosaicism is an intriguing physiological feature of the mammalian brain that generates altered genetic information and provides cellular, and prospectively functional, diversity in a manner similar to that of the immune system. However, both its origin and its physiological significance remain poorly characterized. Most, if not all, cases of somatic mosaicism require prior generation and repair of DNA double strand breaks (DSBs). The relationship between DSB generation, neurogenesis, and early neuronal cell death revealed by our studies in the developing retina provides new perspectives on the different mechanisms that contribute to DNA rearrangements in the developing brain. Here, we speculate on the physiological significance of these findings.

摘要

遗传嵌合是哺乳动物大脑的一个有趣的生理特征,它产生改变的遗传信息,并以类似于免疫系统的方式提供细胞和潜在的功能多样性。然而,其起源和生理意义仍未得到很好的描述。如果不是所有的话,大多数体细胞嵌合体都需要预先产生和修复 DNA 双链断裂 (DSB)。我们在发育中的视网膜中进行的研究揭示了 DSB 的产生、神经发生和早期神经元细胞死亡之间的关系,为导致发育中大脑 DNA 重排的不同机制提供了新的视角。在这里,我们推测这些发现的生理意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f2/9224223/c3d60a66df9d/ijms-23-06449-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f2/9224223/ce90ac35c545/ijms-23-06449-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f2/9224223/c3d60a66df9d/ijms-23-06449-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f2/9224223/ce90ac35c545/ijms-23-06449-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f2/9224223/c3d60a66df9d/ijms-23-06449-g002.jpg

相似文献

1
Exploring the Origin and Physiological Significance of DNA Double Strand Breaks in the Developing Neuroretina.探索发育性神经视网膜中二硫键断裂的起源和生理意义。
Int J Mol Sci. 2022 Jun 9;23(12):6449. doi: 10.3390/ijms23126449.
2
DNA double-strand breaks as drivers of neural genomic change, function, and disease.DNA 双链断裂作为神经基因组改变、功能和疾病的驱动因素。
DNA Repair (Amst). 2018 Nov;71:158-163. doi: 10.1016/j.dnarep.2018.08.019. Epub 2018 Aug 23.
3
Genomic rearrangements induced by unscheduled DNA double strand breaks in somatic mammalian cells.体细胞哺乳动物细胞中未计划的 DNA 双链断裂诱导的基因组重排。
FEBS J. 2017 Aug;284(15):2324-2344. doi: 10.1111/febs.14053. Epub 2017 Mar 22.
4
Imaging Flow Cytometry Quantifies Neural Genome Dynamics.成像流式细胞术定量分析神经基因组动力学。
Cytometry A. 2019 Aug;95(8):825-835. doi: 10.1002/cyto.a.23783. Epub 2019 May 7.
5
Ionizing radiation and genetic risks. XVII. Formation mechanisms underlying naturally occurring DNA deletions in the human genome and their potential relevance for bridging the gap between induced DNA double-strand breaks and deletions in irradiated germ cells.电离辐射与遗传风险。十七、人类基因组中自然发生的 DNA 缺失的形成机制及其在连接诱导的 DNA 双链断裂与照射生殖细胞中的缺失之间的潜在相关性。
Mutat Res. 2013 Oct-Dec;753(2):114-130. doi: 10.1016/j.mrrev.2013.07.003. Epub 2013 Aug 12.
6
The role of nonhomologous DNA end joining, conservative homologous recombination, and single-strand annealing in the cell cycle-dependent repair of DNA double-strand breaks induced by H(2)O(2) in mammalian cells.非同源DNA末端连接、保守同源重组和单链退火在哺乳动物细胞中由H₂O₂诱导的DNA双链断裂的细胞周期依赖性修复中的作用。
Radiat Res. 2008 Dec;170(6):784-93. doi: 10.1667/RR1375.1.
7
Radiation-induced genomic rearrangements formed by nonhomologous end-joining of DNA double-strand breaks.由DNA双链断裂的非同源末端连接形成的辐射诱导基因组重排。
Cancer Res. 2001 May 15;61(10):3886-93.
8
Ku regulates the non-homologous end joining pathway choice of DNA double-strand break repair in human somatic cells.Ku 调控人源体细胞 DNA 双链断裂修复的非同源末端连接途径选择。
PLoS Genet. 2010 Feb 26;6(2):e1000855. doi: 10.1371/journal.pgen.1000855.
9
One end to rule them all: Non-homologous end-joining and homologous recombination at DNA double-strand breaks.一以贯之:DNA 双链断裂处的非同源末端连接和同源重组。
Br J Radiol. 2020 Nov 1;93(1115):20191054. doi: 10.1259/bjr.20191054. Epub 2020 Feb 28.
10
DNA-PK promotes the survival of young neurons in the embryonic mouse retina.DNA-PK 促进胚胎期小鼠视网膜中年轻神经元的存活。
Cell Death Differ. 2010 Nov;17(11):1697-706. doi: 10.1038/cdd.2010.46. Epub 2010 May 7.

引用本文的文献

1
Base excision repair and double strand break repair cooperate to modulate the formation of unrepaired double strand breaks in mouse brain.碱基切除修复和双链断裂修复合作调节小鼠大脑中未修复双链断裂的形成。
Nat Commun. 2024 Sep 4;15(1):7726. doi: 10.1038/s41467-024-51906-5.

本文引用的文献

1
Brain cell somatic gene recombination and its phylogenetic foundations.脑细胞体细胞基因重组及其系统发生基础。
J Biol Chem. 2020 Sep 4;295(36):12786-12795. doi: 10.1074/jbc.REV120.009192. Epub 2020 Jul 22.
2
The role of somatic mosaicism in brain disease.体细胞镶嵌现象在脑部疾病中的作用。
Curr Opin Genet Dev. 2020 Dec;65:84-90. doi: 10.1016/j.gde.2020.05.002. Epub 2020 Jul 1.
3
DNA Double Strand Breaks and Chromosomal Translocations Induced by DNA Topoisomerase II.DNA拓扑异构酶II诱导的DNA双链断裂和染色体易位
Front Mol Biosci. 2019 Dec 10;6:141. doi: 10.3389/fmolb.2019.00141. eCollection 2019.
4
RAG-2 deficiency results in fewer phosphorylated histone H2AX foci, but increased retinal ganglion cell death and altered axonal growth.RAG-2 缺乏导致更少的磷酸化组蛋白 H2AX 焦点,但增加了视网膜神经节细胞死亡和改变轴突生长。
Sci Rep. 2019 Dec 6;9(1):18486. doi: 10.1038/s41598-019-54873-w.
5
Quantitative Analysis of Ku70 and Ku80 mRNA Gene Expression in Melanoma Brain Metastases. Correlation with Immunohistochemistry and Hybridization.黑色素瘤脑转移中Ku70和Ku80 mRNA基因表达的定量分析。与免疫组织化学和杂交的相关性。
Cancer Genomics Proteomics. 2004 May-Jun;1(3):225-230. Epub 2004 May 1.
6
Somatic APP gene recombination in Alzheimer's disease and normal neurons.阿尔茨海默病和正常神经元中的体细胞 APP 基因重组。
Nature. 2018 Nov;563(7733):639-645. doi: 10.1038/s41586-018-0718-6. Epub 2018 Nov 21.
7
Submegabase copy number variations arise during cerebral cortical neurogenesis as revealed by single-cell whole-genome sequencing.单细胞全基因组测序揭示,亚兆碱基级别的拷贝数变异会在大脑皮质神经发生过程中产生。
Proc Natl Acad Sci U S A. 2018 Oct 16;115(42):10804-10809. doi: 10.1073/pnas.1812702115. Epub 2018 Sep 27.
8
DNA double-strand breaks as drivers of neural genomic change, function, and disease.DNA 双链断裂作为神经基因组改变、功能和疾病的驱动因素。
DNA Repair (Amst). 2018 Nov;71:158-163. doi: 10.1016/j.dnarep.2018.08.019. Epub 2018 Aug 23.
9
Genomic mosaicism in the developing and adult brain.发育中和成年大脑中的基因组镶嵌现象。
Dev Neurobiol. 2018 Nov;78(11):1026-1048. doi: 10.1002/dneu.22626. Epub 2018 Aug 1.
10
LINE-1 retrotransposons in healthy and diseased human brain.LINE-1 反转录转座子在健康和患病人类大脑中的分布。
Dev Neurobiol. 2018 May;78(5):434-455. doi: 10.1002/dneu.22567. Epub 2017 Dec 29.