Characterization of New MiniSTR Loci to Aid Analysis of Degraded DNA

Характеристика новых локусов miniSTR для содействия анализу деградированной ДНК
Michael D. Coble, J. M. Butler
2004-11-18

STR triplexesdegraded DNAforensic DNA analysisminiSTR locishort PCR amplicons
A number of studies have demonstrated that successful analysis of degraded DNA specimens from mass disasters or forensic evidence improves with smaller sized polymerase chain reaction (PCR) products. We have scanned the literature for new STR loci, unlinked from the CODIS markers, which can generate amplicons less than 125 bp in size and would therefore be helpful in testing degraded DNA samples. New PCR primers were designed and tested for the STR loci D1S1677, D2S441, D4S2364, D10S1248, D14S1434, and D22S1045, arranged into two miniSTR triplexes. All loci show a moderate degree of polymorphism among 474 U.S. population samples tested and were reliable and sensitive to at least 100 pg of DNA template under controlled laboratory conditions and pristine DNA samples. The utility of these new loci were confirmed in comparing the success of the miniSTR assays for typing degraded bone samples while partial profiles were observed with the majority of the samples using a commercial STR kit.
1
All six loci showed moderate polymorphism across 474 U.S. population samples and reliable sensitivity to at least 100 pg of DNA under controlled conditions.
2
MiniSTR assays improved typing success for degraded bone samples, whereas commercial STR testing produced partial profiles for most samples.
3
Six new, CODIS-unlinked STR loci were identified and redesigned to generate amplicons shorter than 125 bp for degraded-DNA analysis.
4
The findings support these miniSTR loci as useful complementary markers for forensic identification when DNA is highly degraded.
5
The loci D1S1677, D2S441, D4S2364, D10S1248, D14S1434, and D22S1045 were organized into two miniSTR triplex assays.

New miniSTR loci D1S1677, D2S441, D4S2364, D10S1248, D14S1434, and D22S1045 for analysis of degraded DNA specimens

Their polymorphism, amplification reliability and sensitivity, and utility for obtaining genetic profiles from degraded DNA, including bone samples

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2004-11-18
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Michael D. Coble
J. M. Butler
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