New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci

Detalhes bibliográficos
Autor(a) principal: Gomes, Iva
Data de Publicação: 2016
Outros Autores: Brehm, António, Gusmão, Leonor, Schneider, Peter M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.13/2980
Resumo: A great amount of population and forensic genetic data are available for X-STRs supporting the need for having a common and accurate nomenclature among laboratories allowing for better communication, data exchange, and data comparison. DXS10148, DXS10074 and DXS10134 are commonly used X-STRs particularly due to their inclusion in the commercial kit Investigator Argus X-12 (Qiagen). Samples from West Africa and Iraq were sequenced for all three X-STRs allowing the detection of new DNA sequence variants. At DXS10148, variation was detected at four bases downstream from the flanking region from the repeat motif. The sequence AAGG-AAAG has been detected for the first time as a varying (AAGGAAAG)1–3 motif, in the present work. One additional string when compared to the common one (AAGGAAAG)2 adds eight bases to the fragment size of the tetranucleotide STR. This means that 2 repeats are added in these cases to the fragment size of the allele, while the presence of only one copy will reduce the expected allele size by 2 repeats. At DXS10074 two varying stretches consisting of AC and AG dinucleotide repeats were observed in the upstream flanking region, six bases from the main repeat core that also influence the expected allele size. DXS10134 revealed a simpler nomenclature in the Guinea-Bissau sample set when compared to the previously described allele nomenclature. This detected new hidden variation also has impact on the actual allele nomenclature at this locus as it contributes to a new class of short alleles so far undetected in other studies.
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spelling New sequence variants detected at DXS10148, DXS10074 and DXS10134 lociInvestigator Argus X-12X-STRsX chromosomeWest AfricaIraqGuinea-Bissau.Faculdade de Ciências da VidaA great amount of population and forensic genetic data are available for X-STRs supporting the need for having a common and accurate nomenclature among laboratories allowing for better communication, data exchange, and data comparison. DXS10148, DXS10074 and DXS10134 are commonly used X-STRs particularly due to their inclusion in the commercial kit Investigator Argus X-12 (Qiagen). Samples from West Africa and Iraq were sequenced for all three X-STRs allowing the detection of new DNA sequence variants. At DXS10148, variation was detected at four bases downstream from the flanking region from the repeat motif. The sequence AAGG-AAAG has been detected for the first time as a varying (AAGGAAAG)1–3 motif, in the present work. One additional string when compared to the common one (AAGGAAAG)2 adds eight bases to the fragment size of the tetranucleotide STR. This means that 2 repeats are added in these cases to the fragment size of the allele, while the presence of only one copy will reduce the expected allele size by 2 repeats. At DXS10074 two varying stretches consisting of AC and AG dinucleotide repeats were observed in the upstream flanking region, six bases from the main repeat core that also influence the expected allele size. DXS10134 revealed a simpler nomenclature in the Guinea-Bissau sample set when compared to the previously described allele nomenclature. This detected new hidden variation also has impact on the actual allele nomenclature at this locus as it contributes to a new class of short alleles so far undetected in other studies.International Society for Forensic Genetics (ISFG)DigitUMaGomes, IvaBrehm, AntónioGusmão, LeonorSchneider, Peter M.2020-11-13T15:47:09Z20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.13/2980engGomes, I., Brehm, A., Gusmão, L., & Schneider, P. M. (2016). New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci. Forensic Science International: Genetics, 20, 112-116.10.1016/j.fsigen.2015.10.005info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-26T03:38:20Zoai:digituma.uma.pt:10400.13/2980Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:05:49.257490Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
title New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
spellingShingle New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
Gomes, Iva
Investigator Argus X-12
X-STRs
X chromosome
West Africa
Iraq
Guinea-Bissau
.
Faculdade de Ciências da Vida
title_short New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
title_full New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
title_fullStr New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
title_full_unstemmed New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
title_sort New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
author Gomes, Iva
author_facet Gomes, Iva
Brehm, António
Gusmão, Leonor
Schneider, Peter M.
author_role author
author2 Brehm, António
Gusmão, Leonor
Schneider, Peter M.
author2_role author
author
author
dc.contributor.none.fl_str_mv DigitUMa
dc.contributor.author.fl_str_mv Gomes, Iva
Brehm, António
Gusmão, Leonor
Schneider, Peter M.
dc.subject.por.fl_str_mv Investigator Argus X-12
X-STRs
X chromosome
West Africa
Iraq
Guinea-Bissau
.
Faculdade de Ciências da Vida
topic Investigator Argus X-12
X-STRs
X chromosome
West Africa
Iraq
Guinea-Bissau
.
Faculdade de Ciências da Vida
description A great amount of population and forensic genetic data are available for X-STRs supporting the need for having a common and accurate nomenclature among laboratories allowing for better communication, data exchange, and data comparison. DXS10148, DXS10074 and DXS10134 are commonly used X-STRs particularly due to their inclusion in the commercial kit Investigator Argus X-12 (Qiagen). Samples from West Africa and Iraq were sequenced for all three X-STRs allowing the detection of new DNA sequence variants. At DXS10148, variation was detected at four bases downstream from the flanking region from the repeat motif. The sequence AAGG-AAAG has been detected for the first time as a varying (AAGGAAAG)1–3 motif, in the present work. One additional string when compared to the common one (AAGGAAAG)2 adds eight bases to the fragment size of the tetranucleotide STR. This means that 2 repeats are added in these cases to the fragment size of the allele, while the presence of only one copy will reduce the expected allele size by 2 repeats. At DXS10074 two varying stretches consisting of AC and AG dinucleotide repeats were observed in the upstream flanking region, six bases from the main repeat core that also influence the expected allele size. DXS10134 revealed a simpler nomenclature in the Guinea-Bissau sample set when compared to the previously described allele nomenclature. This detected new hidden variation also has impact on the actual allele nomenclature at this locus as it contributes to a new class of short alleles so far undetected in other studies.
publishDate 2016
dc.date.none.fl_str_mv 2016
2016-01-01T00:00:00Z
2020-11-13T15:47:09Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.13/2980
url http://hdl.handle.net/10400.13/2980
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Gomes, I., Brehm, A., Gusmão, L., & Schneider, P. M. (2016). New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci. Forensic Science International: Genetics, 20, 112-116.
10.1016/j.fsigen.2015.10.005
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv International Society for Forensic Genetics (ISFG)
publisher.none.fl_str_mv International Society for Forensic Genetics (ISFG)
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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