Eun Hye Lee, Mingyoung Jeong, Kwangmin Park, Dong Geon Lee, Eun Ju Lee, Haneul Lee, Ah Yeoung Kim, Jae Won Ahn, Hyun Jun Woo, Sunghyun Kim, Jaewon Lim, Jungho Kim
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MicroRNAs (miRNAs or miRs) are small non-coding RNAs that remain relatively stable in the cell nucleus even after death-related changes occur. <b>Objective</b>: This study developed a molecular beacon probe for mmu-miR-133a-5p and assessed its use in mouse muscle tissue at temperatures of 4 °C and 21 °C to estimate the PMI. <b>Methods:</b> A total of 36 healthy adult male BALB/c mice were divided into 9 PMI time points (0, 2, 6, 8, and 10 days) with 3 mice per time point, and they were exposed to 4 °C and 21 °C. Next, the expression pattern of mmu-miR-133a in the skeletal muscle tissue over a 10-day PMI period was analyzed using the developed molecular beacon probe. <b>Results:</b> The molecular beacon (MB) probe was designed for optimal thermodynamic stability with a hairpin structure that opened in the presence of mmu-miR-133a-5p, thus separating the fluorophore from the quencher and resulting in a strong fluorescence signal at 495 nm. Fluorescence intensity increased with mmu-miR-133a-5p concentration from 1 ng/μL to 1000 ng/μL and exhibited a strong correlation (R<sup>2</sup> = 0.9966) and a detection limit of 1 ng/μL. Subsequently, the expression level of mmu-miR-133a-5p was observed to be stable in mouse skeletal muscle tissue at both 4 °C and 21 °C. <b>Conclusions:</b> This user-friendly assay can complete measurements in just 30 min after RNA extraction and is suitable for point-of-care testing, and it possesses the potential to improve existing complex and time-consuming methods for PMI estimation.</p>","PeriodicalId":19271,"journal":{"name":"Non-Coding RNA","volume":"10 6","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11676884/pdf/","citationCount":"0","resultStr":"{\"title\":\"Detection of miR-133a-5p Using a Molecular Beacon Probe for Investigating Postmortem Intervals.\",\"authors\":\"Eun Hye Lee, Mingyoung Jeong, Kwangmin Park, Dong Geon Lee, Eun Ju Lee, Haneul Lee, Ah Yeoung Kim, Jae Won Ahn, Hyun Jun Woo, Sunghyun Kim, Jaewon Lim, Jungho Kim\",\"doi\":\"10.3390/ncrna10060058\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Background:</b> When a body is discovered at a crime or murder scene, it is crucial to examine the body and estimate its postmortem interval (PMI). 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引用次数: 0
摘要
背景:当在犯罪或谋杀现场发现尸体时,对尸体进行检查并估计其死后间隔(PMI)是至关重要的。准确估计PMI对于识别嫌疑人和提供破案线索至关重要。MicroRNAs (miRNAs或miRs)是一种小的非编码rna,即使在死亡相关的变化发生后,也能在细胞核中保持相对稳定。目的:本研究开发了一种针对mum - mir -133a-5p的分子信标探针,并评估了其在4°C和21°C温度下在小鼠肌肉组织中的应用,以估计PMI。方法:选取健康成年雄性BALB/c小鼠36只,分为9个PMI时间点(0、2、6、8、10天),每个时间点3只,分别暴露于4℃和21℃环境。接下来,使用开发的分子信标探针分析10天PMI期间骨骼肌组织中mum - mir -133a的表达模式。结果:设计的分子信标(MB)探针具有最佳的热力学稳定性,其发夹结构在mmu-miR-133a-5p存在下打开,从而将荧光团从猝灭剂中分离出来,并在495 nm处产生强荧光信号。荧光强度随mmu- mir - 133p -5p浓度从1 ng/μL增加到1000 ng/μL,呈强相关(R2 = 0.9966),检出限为1 ng/μL。随后,我们观察到mmu-miR-133a-5p在小鼠骨骼肌组织中在4°C和21°C下的表达水平是稳定的。结论:这种用户友好的检测方法可以在RNA提取后30分钟内完成测量,适用于即时检测,并且具有改进现有复杂且耗时的PMI估计方法的潜力。
Detection of miR-133a-5p Using a Molecular Beacon Probe for Investigating Postmortem Intervals.
Background: When a body is discovered at a crime or murder scene, it is crucial to examine the body and estimate its postmortem interval (PMI). Accurate estimation of PMI is vital for identifying suspects and providing clues to resolve the case. MicroRNAs (miRNAs or miRs) are small non-coding RNAs that remain relatively stable in the cell nucleus even after death-related changes occur. Objective: This study developed a molecular beacon probe for mmu-miR-133a-5p and assessed its use in mouse muscle tissue at temperatures of 4 °C and 21 °C to estimate the PMI. Methods: A total of 36 healthy adult male BALB/c mice were divided into 9 PMI time points (0, 2, 6, 8, and 10 days) with 3 mice per time point, and they were exposed to 4 °C and 21 °C. Next, the expression pattern of mmu-miR-133a in the skeletal muscle tissue over a 10-day PMI period was analyzed using the developed molecular beacon probe. Results: The molecular beacon (MB) probe was designed for optimal thermodynamic stability with a hairpin structure that opened in the presence of mmu-miR-133a-5p, thus separating the fluorophore from the quencher and resulting in a strong fluorescence signal at 495 nm. Fluorescence intensity increased with mmu-miR-133a-5p concentration from 1 ng/μL to 1000 ng/μL and exhibited a strong correlation (R2 = 0.9966) and a detection limit of 1 ng/μL. Subsequently, the expression level of mmu-miR-133a-5p was observed to be stable in mouse skeletal muscle tissue at both 4 °C and 21 °C. Conclusions: This user-friendly assay can complete measurements in just 30 min after RNA extraction and is suitable for point-of-care testing, and it possesses the potential to improve existing complex and time-consuming methods for PMI estimation.
Non-Coding RNABiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
6.70
自引率
4.70%
发文量
74
审稿时长
10 weeks
期刊介绍:
Functional studies dealing with identification, structure-function relationships or biological activity of: small regulatory RNAs (miRNAs, siRNAs and piRNAs) associated with the RNA interference pathway small nuclear RNAs, small nucleolar and tRNAs derived small RNAs other types of small RNAs, such as those associated with splice junctions and transcription start sites long non-coding RNAs, including antisense RNAs, long ''intergenic'' RNAs, intronic RNAs and ''enhancer'' RNAs other classes of RNAs such as vault RNAs, scaRNAs, circular RNAs, 7SL RNAs, telomeric and centromeric RNAs regulatory functions of mRNAs and UTR-derived RNAs catalytic and allosteric (riboswitch) RNAs viral, transposon and repeat-derived RNAs bacterial regulatory RNAs, including CRISPR RNAS Analysis of RNA processing, RNA binding proteins, RNA signaling and RNA interaction pathways: DICER AGO, PIWI and PIWI-like proteins other classes of RNA binding and RNA transport proteins RNA interactions with chromatin-modifying complexes RNA interactions with DNA and other RNAs the role of RNA in the formation and function of specialized subnuclear organelles and other aspects of cell biology intercellular and intergenerational RNA signaling RNA processing structure-function relationships in RNA complexes RNA analyses, informatics, tools and technologies: transcriptomic analyses and technologies development of tools and technologies for RNA biology and therapeutics Translational studies involving long and short non-coding RNAs: identification of biomarkers development of new therapies involving microRNAs and other ncRNAs clinical studies involving microRNAs and other ncRNAs.