Female sample screening using colorimetric reverse transcription loop-mediated isothermal amplification (RT-LAMP)
Seiji Kubo1, Keito Amai2, Jin Tanaka2
1Department of Clinical Laboratory and Molecular Pathology, Faculty of Medicine, Academic Assembly, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan; Forensic Science Laboratory, Ishikawa Prefectural Police Headquarters, 1-1 Kuratsuki, Kanazawa 920-8553, Japan.
This study presents a new colorimetric assay for rapidly screening female forensic samples. The assay targets XIST RNA, offering a simple and effective method for identifying female DNA contributions.
Area of Science:
- Forensic Science
- Molecular Biology
- Genetics
Background:
- Effective DNA typing workflows rely on accurate forensic sample screening.
- Detecting sex-specific markers is crucial for forensic analysis.
- Current DNA-based methods struggle to confirm female contributions in forensic samples.
Purpose of the Study:
- To develop a novel assay for the specific screening of female forensic samples.
- To address the limitations of existing DNA-based methods for detecting female DNA.
- To provide a rapid and simple tool for forensic casework.
Main Methods:
- Development of a colorimetric reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay.
- Targeting the X-inactive specific transcript (XIST) long non-coding RNA for detection.
- Assay operation at 65°C for 30 minutes with visual pH indicator dye readout.
Main Results:
- The assay demonstrated a detection limit of approximately 0.5 µL of blood.
- Successful detection of XIST RNA in mixed body fluids and mock forensic samples.
- Results were discernible through a simple color change, indicating assay functionality.
Conclusions:
- The developed RT-LAMP assay provides a rapid and simple strategy for screening female samples.
- The assay shows potential applicability for real-world forensic casework.
- This method enhances the ability to confirm female contributions in forensic investigations.
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