• 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

人类基因组中的 CRISPR 在肿瘤组织附近的恶性和正常组织中表达水平不同。

CRISPRs in the human genome are differentially expressed between malignant and normal adjacent to tumor tissue.

机构信息

Department of Urology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, Netherlands.

Cancer Computational Biology Center, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, Netherlands.

出版信息

Commun Biol. 2022 Apr 8;5(1):338. doi: 10.1038/s42003-022-03249-4.

DOI:10.1038/s42003-022-03249-4
PMID:35396392
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8993844/
Abstract

Clustered Regularly Interspaced Short Palindromic Repeats (CRISPRs) have been identified in bacteria, archaea and mitochondria of plants, but not in eukaryotes. Here, we report the discovery of 12,572 putative CRISPRs randomly distributed across the human chromosomes, which we termed hCRISPRs. By using available transcriptome datasets, we demonstrate that hCRISPRs are distinctively expressed as small non-coding RNAs (sncRNAs) in cell lines and human tissues. Moreover, expression patterns thereof enabled us to distinguish normal from malignant tissues. In prostate cancer, we confirmed the differential hCRISPR expression between normal adjacent and malignant primary prostate tissue by RT-qPCR and demonstrate that the SHERLOCK and DETECTR dipstick tools are suitable to detect these sncRNAs. We anticipate that the discovery of CRISPRs in the human genome can be further exploited for diagnostic purposes in cancer and other medical conditions, which certainly will lead to the development of point-of-care tests based on the differential expression of the hCRISPRs.

摘要

已在细菌、古菌和植物的线粒体中鉴定出了成簇的规律间隔的短回文重复序列(CRISPRs),但在真核生物中尚未发现。在这里,我们报告了在人类染色体上随机分布的 12572 个推定的 CRISPR 的发现,我们将其称为 hCRISPR。通过使用现有的转录组数据集,我们证明 hCRISPR 作为细胞系和人体组织中的小非编码 RNA(sncRNA)表现出明显的表达。此外,它们的表达模式使我们能够区分正常组织和恶性组织。在前列腺癌中,我们通过 RT-qPCR 证实了正常相邻和恶性原发性前列腺组织之间 hCRISPR 的差异表达,并证明 SHERLOCK 和 DETECTR 棒式工具适合检测这些 sncRNA。我们预计,人类基因组中 CRISPR 的发现可以进一步用于癌症和其他医疗条件的诊断目的,这肯定会导致基于 hCRISPR 差异表达的即时检测的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/af05a1873d4f/42003_2022_3249_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/64be56c9e02a/42003_2022_3249_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/e468517b83f7/42003_2022_3249_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/36de0b76d3fb/42003_2022_3249_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/dcfe533e9938/42003_2022_3249_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/35d07748b4df/42003_2022_3249_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/cd2d0687228b/42003_2022_3249_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/af05a1873d4f/42003_2022_3249_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/64be56c9e02a/42003_2022_3249_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/e468517b83f7/42003_2022_3249_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/36de0b76d3fb/42003_2022_3249_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/dcfe533e9938/42003_2022_3249_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/35d07748b4df/42003_2022_3249_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/cd2d0687228b/42003_2022_3249_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b60/8993844/af05a1873d4f/42003_2022_3249_Fig7_HTML.jpg

相似文献

1
CRISPRs in the human genome are differentially expressed between malignant and normal adjacent to tumor tissue.人类基因组中的 CRISPR 在肿瘤组织附近的恶性和正常组织中表达水平不同。
Commun Biol. 2022 Apr 8;5(1):338. doi: 10.1038/s42003-022-03249-4.
2
Clarifying CRISPR: Why Repeats Identified in the Human Genome Should Not Be Considered CRISPRs.厘清 CRISPR:人类基因组中鉴定出的重复序列不应被视为 CRISPR 系统。
CRISPR J. 2023 Jun;6(3):216-221. doi: 10.1089/crispr.2022.0106. Epub 2023 Apr 11.
3
Clustered regularly interspaced short palindromic repeats (CRISPRs): the hallmark of an ingenious antiviral defense mechanism in prokaryotes.成簇规律间隔短回文重复序列(CRISPRs):原核生物中一种巧妙抗病毒防御机制的标志。
Biol Chem. 2011 Apr;392(4):277-89. doi: 10.1515/BC.2011.042. Epub 2011 Feb 7.
4
Development of a novel molecular detection method for clustered regularly interspaced short palindromic repeats (CRISPRs) in Taylorella organisms.泰勒氏菌属生物中规律成簇间隔短回文重复序列(CRISPRs)新型分子检测方法的开发
J Med Microbiol. 2015 Jul;64(7):782-787. doi: 10.1099/jmm.0.000079. Epub 2015 May 1.
5
CRISPRCasdb a successor of CRISPRdb containing CRISPR arrays and cas genes from complete genome sequences, and tools to download and query lists of repeats and spacers.CRISPRCasdb 是 CRISPRdb 的一个后继者,包含来自完整基因组序列的 CRISPR 阵列和 cas 基因,以及用于下载和查询重复序列和间隔区列表的工具。
Nucleic Acids Res. 2020 Jan 8;48(D1):D535-D544. doi: 10.1093/nar/gkz915.
6
History of CRISPR-Cas from Encounter with a Mysterious Repeated Sequence to Genome Editing Technology.CRISPR-Cas 的历史:从与神秘重复序列的偶然相遇到基因组编辑技术。
J Bacteriol. 2018 Mar 12;200(7). doi: 10.1128/JB.00580-17. Print 2018 Apr 1.
7
Small regulatory RNAs in Archaea.古菌中的小调控RNA。
RNA Biol. 2014;11(5):484-93. doi: 10.4161/rna.28452. Epub 2014 Mar 31.
8
Genome DNA Sequence Variation, Evolution, and Function in Bacteria and Archaea.细菌和古菌中的基因组DNA序列变异、进化与功能
Curr Issues Mol Biol. 2013;15:19-24. Epub 2012 Jul 6.
9
Diverse CRISPRs evolving in human microbiomes.人类微生物组中多样化的 CRISPR 系统。
PLoS Genet. 2012;8(6):e1002441. doi: 10.1371/journal.pgen.1002441. Epub 2012 Jun 13.
10
[Advances in clustered regularly interspaced short palindromic repeats--a review].[成簇规律间隔短回文重复序列的研究进展——综述]
Wei Sheng Wu Xue Bao. 2011 Aug;51(8):1007-13.

引用本文的文献

1
Clarifying CRISPR: Why Repeats Identified in the Human Genome Should Not Be Considered CRISPRs.厘清 CRISPR:人类基因组中鉴定出的重复序列不应被视为 CRISPR 系统。
CRISPR J. 2023 Jun;6(3):216-221. doi: 10.1089/crispr.2022.0106. Epub 2023 Apr 11.
2
A Compendium of AR Splice Variants in Metastatic Castration-Resistant Prostate Cancer.转移性去势抵抗性前列腺癌中的 AR 剪接变体概述。
Int J Mol Sci. 2023 Mar 22;24(6):6009. doi: 10.3390/ijms24066009.

本文引用的文献

1
Alternative functions of CRISPR-Cas systems in the evolutionary arms race.CRISPR-Cas 系统在进化军备竞赛中的替代功能。
Nat Rev Microbiol. 2022 Jun;20(6):351-364. doi: 10.1038/s41579-021-00663-z. Epub 2022 Jan 6.
2
Fusion transcripts and their genomic breakpoints in polyadenylated and ribosomal RNA-minus RNA sequencing data.多聚腺苷酸化和核糖体 RNA-减 RNA 测序数据中的融合转录本及其基因组断点。
Gigascience. 2021 Dec 9;10(12). doi: 10.1093/gigascience/giab080.
3
Transposon-associated TnpB is a programmable RNA-guided DNA endonuclease.
转座子相关的 TnpB 是一种可编程的 RNA 引导的 DNA 内切酶。
Nature. 2021 Nov;599(7886):692-696. doi: 10.1038/s41586-021-04058-1. Epub 2021 Oct 7.
4
The widespread IS200/IS605 transposon family encodes diverse programmable RNA-guided endonucleases.广泛存在的 IS200/IS605 转座子家族编码了多种可编程 RNA 指导的内切核酸酶。
Science. 2021 Oct;374(6563):57-65. doi: 10.1126/science.abj6856. Epub 2021 Sep 9.
5
CRISPRloci: comprehensive and accurate annotation of CRISPR-Cas systems.CRISPR 基因座:CRISPR-Cas 系统的全面准确注释。
Nucleic Acids Res. 2021 Jul 2;49(W1):W125-W130. doi: 10.1093/nar/gkab456.
6
CRISPRCasTyper: Automated Identification, Annotation, and Classification of CRISPR-Cas Loci.CRISPRCasTyper:CRISPR-Cas 基因座的自动识别、注释和分类。
CRISPR J. 2020 Dec;3(6):462-469. doi: 10.1089/crispr.2020.0059. Epub 2020 Dec 4.
7
Guide-free Cas9 from pathogenic bacteria causes severe damage to DNA.无向导 Cas9 源自致病性细菌,可导致 DNA 严重损伤。
Sci Adv. 2020 Jun 17;6(25):eaaz4849. doi: 10.1126/sciadv.aaz4849. eCollection 2020 Jun.
8
SHERLOCK: nucleic acid detection with CRISPR nucleases.利用 CRISPR 核酸酶进行核酸检测。
Nat Protoc. 2019 Oct;14(10):2986-3012. doi: 10.1038/s41596-019-0210-2. Epub 2019 Sep 23.
9
Molecular characterization of colorectal adenomas reveals POFUT1 as a candidate driver of tumor progression.结直肠腺瘤的分子特征分析揭示 POFUT1 是肿瘤进展的候选驱动基因。
Int J Cancer. 2020 Apr 1;146(7):1979-1992. doi: 10.1002/ijc.32627. Epub 2019 Aug 30.
10
Catalytically Active Cas9 Mediates Transcriptional Interference to Facilitate Bacterial Virulence.催化活性 Cas9 介导转录干扰以促进细菌毒力。
Mol Cell. 2019 Aug 8;75(3):498-510.e5. doi: 10.1016/j.molcel.2019.05.029. Epub 2019 Jun 27.