Literature DB >> 24997322

Assessing PreCR™ repair enzymes for restoration of STR profiles from artificially degraded DNA for human identification.

James M Robertson1, Shauna M Dineen2, Kristina A Scott2, Jonathan Lucyshyn3, Maria Saeed2, Devonie L Murphy2, Andrew J Schweighardt2, Kelly A Meiklejohn2.   

Abstract

Forensic scientists have used several approaches to obtain short tandem repeat (STR) profiles from compromised DNA samples, including supplementing the polymerase chain reaction (PCR) with enhancers and using procedures yielding reduced-length amplicons. For degraded DNA, the peak intensities of the alleles separated by electrophoresis generally decrease as the length of the allele increases. When the intensities of the alleles decrease below an established threshold, they are described as drop-outs, thus contributing to a partial STR profile. This work assesses the use of repair enzymes to improve the STR profiles from artificially degraded DNA. The commercial PreCR™ repair kit of DNA repair enzymes was tested on both purified DNA and native DNA in body fluids exposed to oxidizing agents, hydrolytic conditions, ultraviolet (UV) and ionizing radiation, and desiccation. The strategy was to restrict the level of DNA damage to that which yields partial STR profiles in order to test for allele restoration as opposed to simple allele enhancement. Two protocols were investigated for allele restoration: a sequential protocol using the manufacturer's repair procedure and a modified protocol reportedly designed for optimal STR analysis of forensic samples. Allele restoration was obtained with both protocols, but the peak height appeared to be higher for the modified protocol (determined by Mann-Kendall Trend Test). The success of the approach using the PreCR™ repair enzymes was sporadic; it led to allele restoration as well as allele drop-out. Additionally, allele restoration with the PreCR™ enzymes was compared with restoration by alternative, but commonly implemented approaches using Restorase™, PCRBoost™, bovine serum albumin (BSA) and the Minifiler™ STR system. The alternative methods were also successful in improving the STR profile, but their success also depended on the quality of the template encountered. Our results indicate the PreCR™ repair kit may be useful for restoring STR profiles from damaged DNA, but further work is required to develop a generalized approach. Published by Elsevier Ireland Ltd.

Entities:  

Keywords:  DNA repair; Degraded DNA; Degraded DNA reference sample; Forensic biology; PreCR™ Repair Mix; Short tandem repeat (STR) analysis

Mesh:

Year:  2014        PMID: 24997322     DOI: 10.1016/j.fsigen.2014.05.011

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  6 in total

1.  Genotyping DNA isolated from UV irradiated human bloodstains using whole genome amplification.

Authors:  Seisaku Uchigasaki; Jian Tie; Erina Sobashima; Naomi Shimada
Journal:  Mol Biol Rep       Date:  2018-07-07       Impact factor: 2.316

2.  Information decay and enzymatic information recovery for DNA data storage.

Authors:  Linda C Meiser; Andreas L Gimpel; Tejas Deshpande; Gabriela Libort; Weida D Chen; Reinhard Heckel; Bichlien H Nguyen; Karin Strauss; Wendelin J Stark; Robert N Grass
Journal:  Commun Biol       Date:  2022-10-20

3.  Comparison of different methods for repairing damaged DNA from buffered and unbuffered formalin-fixed tissues.

Authors:  Yuxuan Liu; Huayu He; Shaohua Yi; Qingqing Hu; Wenqiong Zhang; Daixin Huang
Journal:  Int J Legal Med       Date:  2017-08-30       Impact factor: 2.686

4.  Enrichment of fetal and maternal long cell-free DNA fragments from maternal plasma following DNA repair.

Authors:  Joaquim S L Vong; Peiyong Jiang; Suk-Hang Cheng; Wing-Shan Lee; Jason C H Tsang; Tak-Yeung Leung; K C Allen Chan; Rossa W K Chiu; Y M Dennis Lo
Journal:  Prenat Diagn       Date:  2019-01-10       Impact factor: 3.050

Review 5.  Potential applications of microRNA profiling to forensic investigations.

Authors:  Claire L Glynn
Journal:  RNA       Date:  2019-10-28       Impact factor: 4.942

6.  Engineered viral DNA polymerase with enhanced DNA amplification capacity: a proof-of-concept of isothermal amplification of damaged DNA.

Authors:  Carlos D Ordóñez; Ana Lechuga; Margarita Salas; Modesto Redrejo-Rodríguez
Journal:  Sci Rep       Date:  2020-09-14       Impact factor: 4.379

  6 in total

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