Literature DB >> 16514543

Multistep microsatellite mutation in the maternally transmitted locus D13S317: a case of maternal allele mismatch in the child.

Devinder Singh Negi1, Mahfooz Alam, S Annapurna Bhavani, Javaregowda Nagaraju.   

Abstract

Examination of a case of a paternity dispute with 17 autosomal short tandem repeats (STR) loci revealed a mismatch of the maternally transmitted allele at the locus D13S317 in the questioned child. The composition of the alleles of this locus in the mother, questioned child and suspected father was 8/8, 11/11 and 8/11, respectively. The sequence analysis of the regions flanking the locus D13S317 and peak height measurements of the paternal, maternal and child alleles at this locus excluded the possibility of null allele as a cause of the allelic mismatch inherited by the child. The results suggested expansion of the microsatellite repeat motif, TATC by three repeat units as a probable cause for the allelic mismatch in the child. This is a rare case of maternally transmitted multistep microsatellite mutation reported for the first time for this locus in the forensic DNA analysis. The mutation rate at D13S317 locus in maternal and paternal meiosis was 0.04 and 0.14%, respectively, and overall mutation rate was 0.15%. The probability of maternity and paternity were 0.999999 and 0.999999, respectively, for all the 17 autosomal STR loci analyzed. Furthermore, the sequence of two hypervariable regions of mitochondrial DNA, HV1 and HV2 and the maternal alleles of six X chromosome STR loci in the questioned child matched completely with the mother. These results conclusively proved that the mother and suspected father are the biological parents of the questioned child.

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Year:  2006        PMID: 16514543     DOI: 10.1007/s00414-006-0080-3

Source DB:  PubMed          Journal:  Int J Legal Med        ISSN: 0937-9827            Impact factor:   2.686


  29 in total

1.  Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs.

Authors:  M Kayser; L Roewer; M Hedman; L Henke; J Henke; S Brauer; C Krüger; M Krawczak; M Nagy; T Dobosz; R Szibor; P de Knijff; M Stoneking; A Sajantila
Journal:  Am J Hum Genet       Date:  2000-04-06       Impact factor: 11.025

2.  Validation of a 16-locus fluorescent multiplex system.

Authors:  Benjamin E Krenke; Allan Tereba; Stacey J Anderson; Eric Buel; Sherry Culhane; Carla J Finis; Christine S Tomsey; Jeffrey M Zachetti; Arni Masibay; Dawn R Rabbach; Elizabeth A Amiott; Cynthia J Sprecher
Journal:  J Forensic Sci       Date:  2002-07       Impact factor: 1.832

3.  Allelic drop-out in the STR system ACTBP2 (SE33) as a result of mutations in the primer binding region.

Authors:  Marielle Heinrich; Miriam Müller; Steven Rand; Bernd Brinkmann; Carsten Hohoff
Journal:  Int J Legal Med       Date:  2004-08-20       Impact factor: 2.686

4.  Slippage synthesis of simple sequence DNA.

Authors:  C Schlötterer; D Tautz
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

5.  The relationship between microsatellite slippage mutation rate and the number of repeat units.

Authors:  Yinglei Lai; Fengzhu Sun
Journal:  Mol Biol Evol       Date:  2003-08-29       Impact factor: 16.240

6.  Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat.

Authors:  B Brinkmann; M Klintschar; F Neuhuber; J Hühne; B Rolf
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

7.  Evaluation of Y-chromosomal STRs: a multicenter study.

Authors:  M Kayser; A Caglià; D Corach; N Fretwell; C Gehrig; G Graziosi; F Heidorn; S Herrmann; B Herzog; M Hidding; K Honda; M Jobling; M Krawczak; K Leim; S Meuser; E Meyer; W Oesterreich; A Pandya; W Parson; G Penacino; A Perez-Lezaun; A Piccinini; M Prinz; C Schmitt; L Roewer
Journal:  Int J Legal Med       Date:  1997       Impact factor: 2.686

8.  Mutation of human short tandem repeats.

Authors:  J L Weber; C Wong
Journal:  Hum Mol Genet       Date:  1993-08       Impact factor: 6.150

9.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

10.  Male-driven evolution of DNA sequences.

Authors:  L C Shimmin; B H Chang; W H Li
Journal:  Nature       Date:  1993-04-22       Impact factor: 49.962

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  2 in total

1.  Haplotype-assisted characterization of germline mutations at short tandem repeat loci.

Authors:  Miriam Müller; Ulla Sibbing; Carsten Hohoff; Bernd Brinkmann
Journal:  Int J Legal Med       Date:  2009-11-11       Impact factor: 2.686

2.  Identification and sequence analysis of discordant phenotypes between AmpFlSTR SGM Plus and PowerPlex 16.

Authors:  Nancy Vanderheyden; Ahnly Mai; Anja Gilissen; Jean-Jacques Cassiman; Ronny Decorte
Journal:  Int J Legal Med       Date:  2007-04-04       Impact factor: 2.791

  2 in total

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