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使用分子信标探针检测miR-133a-5p以研究死亡时间间隔

Detection of miR-133a-5p Using a Molecular Beacon Probe for Investigating Postmortem Intervals.

作者信息

Lee Eun Hye, Jeong Mingyoung, Park Kwangmin, Lee Dong Geon, Lee Eun Ju, Lee Haneul, Kim Ah Yeoung, Ahn Jae Won, Woo Hyun Jun, Kim Sunghyun, Lim Jaewon, Kim Jungho

机构信息

Department of Forensic Science, Graduate School, Catholic University of Pusan, Busan 46252, Republic of Korea.

Next-Generation Industrial Field-Based Specialist Program for Molecular Diagnostics, Brain Busan 21 Plus Project, Graduate School, Catholic University of Pusan, Busan 46252, Republic of Korea.

出版信息

Noncoding RNA. 2024 Nov 26;10(6):58. doi: 10.3390/ncrna10060058.

Abstract

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. : 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. 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. 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 = 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. 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.

摘要

当在犯罪或谋杀现场发现尸体时,检查尸体并估计其死后间隔时间(PMI)至关重要。准确估计PMI对于识别嫌疑人以及提供破案线索至关重要。微小RNA(miRNA或miR)是小的非编码RNA,即使在发生与死亡相关的变化后,它们在细胞核中仍保持相对稳定。本研究开发了一种用于mmu-miR-133a-5p的分子信标探针,并评估了其在4℃和21℃温度下在小鼠肌肉组织中用于估计PMI的情况。总共36只健康成年雄性BALB/c小鼠被分为9个PMI时间点(0、2、6、8和10天),每个时间点3只小鼠,并将它们置于4℃和21℃环境中。接下来,使用开发的分子信标探针分析了在10天PMI期间骨骼肌组织中mmu-miR-133a的表达模式。分子信标(MB)探针被设计为具有最佳热力学稳定性,其发夹结构在mmu-miR-133a-5p存在时打开,从而使荧光团与猝灭剂分离,并在495nm处产生强烈的荧光信号。荧光强度随mmu-miR-133a-5p浓度从1ng/μL增加到1000ng/μL而增加,并表现出强相关性(R = 0.9966),检测限为1ng/μL。随后,观察到mmu-miR-133a-5p在4℃和21℃的小鼠骨骼肌组织中的表达水平均稳定。这种用户友好的检测方法在RNA提取后仅30分钟即可完成测量,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。

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