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

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作者
Job van Riet
Chinmoy Saha
Nikolaos Strepis
Rutger W. W. Brouwer
Elena S. Martens-Uzunova
Wesley S. van de Geer
Sigrid M. A. Swagemakers
Andrew Stubbs
Yassir Halimi
Sanne Voogd
Arif Mohammad Tanmoy
Malgorzata A. Komor
Youri Hoogstrate
Bart Janssen
Remond J. A. Fijneman
Yashar S. Niknafs
Arul M. Chinnaiyan
Wilfred F. J. van IJcken
Peter J. van der Spek
Guido Jenster
Rogier Louwen
机构
[1] University Medical Center Rotterdam,Department of Urology, Erasmus MC Cancer Institute
[2] University Medical Center Rotterdam,Cancer Computational Biology Center, Erasmus MC Cancer Institute
[3] University Medical Center Rotterdam,Department of Medical Oncology, Erasmus MC Cancer Institute
[4] Erasmus University Medical Center Rotterdam,Department of Medical Microbiology and Infectious Diseases
[5] Erasmus University Medical Center Rotterdam,Center for Biomics
[6] Erasmus University Medical Center Rotterdam,Clinical Bioinformatics, Department of Pathology
[7] Child Health Research Foundation,Translational Gastrointestinal Oncology, Department of Pathology
[8] Netherlands Cancer Institute,Oncoproteomics Laboratory, Department of Medical Oncology
[9] VU University Medical Center,Department of Neurology
[10] Erasmus University Medical Center Rotterdam,Michigan Center for Translational Pathology
[11] GenomeScan,undefined
[12] University of Michigan,undefined
来源
Communications Biology | / 5卷
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摘要
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.
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共 114 条
[1]  
Nakata A(1989)Unusual nucleotide arrangement with repeated sequences in the J. Bacteriol. 171 3553-3556
[2]  
Amemura M(1993) K-12 chromosome Mol. Microbiol. 10 1057-1065
[3]  
Makino K(1995)va. Nature of DNA polymorphism in the direct repeat cluster of Mol. Microbiol. 17 85-93
[4]  
Groenen PMA(2000); application for strain differentiation by a novel typing method Mol. Microbiol. 36 244-246
[5]  
Bunschoten AE(1998)Long stretches of short tandem repeats are present in the largest replicons of the Archaea Microbiol. Mol. Biol. Rev. 62 275-293
[6]  
van Soolingen D(2000) and J. Bacteriol. 182 2393-2401
[7]  
Errtbden JDA(2001) and could be involved in replicon partitioning Proc. Natl Acad. Sci. USA 98 7835-7840
[8]  
Mojica FJMM(2002)Biological significance of a family of regularly spaced repeats in the genomes of Archaea, Bacteria and mitochondria Mol. Microbiol. 43 1565-1575
[9]  
Ferrer C(2019)Short-sequence DNA repeats in prokaryotic genomes Mol. Cell 75 498-510.e5
[10]  
Juez G(2014)Genetic variation and evolutionary origin of the direct repeat locus of Microbiol. Mol. Biol. Rev. 78 74-88