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Transcriptomic population markers for human population discrimination

BACKGROUND: Numerous studies have demonstrated significant differences in the expression level across continental human populations. Most of published results were performed on B-cell lines materials examined under specific laboratory conditions, without further validation in a primary biological ma...

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Autores principales: Daca-Roszak, P., Swierniak, M., Jaksik, R., Tyszkiewicz, T., Oczko-Wojciechowska, M., Zebracka-Gala, J., Jarzab, B., Witt, M., Zietkiewicz, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081795/
https://www.ncbi.nlm.nih.gov/pubmed/30086702
http://dx.doi.org/10.1186/s12863-018-0663-2
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author Daca-Roszak, P.
Swierniak, M.
Jaksik, R.
Tyszkiewicz, T.
Oczko-Wojciechowska, M.
Zebracka-Gala, J.
Jarzab, B.
Witt, M.
Zietkiewicz, E.
author_facet Daca-Roszak, P.
Swierniak, M.
Jaksik, R.
Tyszkiewicz, T.
Oczko-Wojciechowska, M.
Zebracka-Gala, J.
Jarzab, B.
Witt, M.
Zietkiewicz, E.
author_sort Daca-Roszak, P.
collection PubMed
description BACKGROUND: Numerous studies have demonstrated significant differences in the expression level across continental human populations. Most of published results were performed on B-cell lines materials examined under specific laboratory conditions, without further validation in a primary biological material. The goal of our study was to identify mRNA markers characterized by a significant and stable difference in the gene expression profile in Caucasian and Chinese populations, both in the commercially available B-lymphocyte cell lines and in the primary samples of the peripheral blood. RESULTS: The preliminary selection of population-differentiating transcripts was based on Illumina expression microarray analysis of the representative group of ethnically-specified B-lymphocyte cell lines. Twenty genes with the inter-population difference in the mean expression characterized by the at least 1.5-fold change and FDR <  0.05 were identified. Subsequently, a two-step validation procedure was carried out. In the first step, a subset of selected population- differentiating transcripts was tested in the independent set of B-lymphocyte cell lines, using TLDA cards. Based on TLDA analysis, three transcripts representing Fch > 2 were chosen for validation. The differentiating status was confirmed for all of them: UTS2, UGT2B17 and SLC7A7. The mean expression of UTS2 was higher in CHB (25.8-fold change compared to CEU), while the expression of UGT2B17 and SLC7A7 was higher in CEU (3.2- and 2.2-fold change, respectively). In the next validation step, two transcripts were verified in the primary biological material. As an ultimate result of our study, two mRNA markers (UTS2 and UGT2B17) exhibiting population differences in the expression level in both B-cell line and in the blood were identified. Further statistical analysis confirmed the discriminatory potential of these two markers. CONCLUSIONS: An inter-population differences on the level of gene expression were identified in both B-cell lines and peripheral blood samples. These findings may have a practical application in the field of forensic science. In particular, these transcripts, targeted by specific probes, may be used as population-specific targets in the efforts aiming to separate mixture of blood from individuals of different populations. Notwithstanding, these results have to be confirmed on extended population group. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-018-0663-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-60817952018-08-09 Transcriptomic population markers for human population discrimination Daca-Roszak, P. Swierniak, M. Jaksik, R. Tyszkiewicz, T. Oczko-Wojciechowska, M. Zebracka-Gala, J. Jarzab, B. Witt, M. Zietkiewicz, E. BMC Genet Research Article BACKGROUND: Numerous studies have demonstrated significant differences in the expression level across continental human populations. Most of published results were performed on B-cell lines materials examined under specific laboratory conditions, without further validation in a primary biological material. The goal of our study was to identify mRNA markers characterized by a significant and stable difference in the gene expression profile in Caucasian and Chinese populations, both in the commercially available B-lymphocyte cell lines and in the primary samples of the peripheral blood. RESULTS: The preliminary selection of population-differentiating transcripts was based on Illumina expression microarray analysis of the representative group of ethnically-specified B-lymphocyte cell lines. Twenty genes with the inter-population difference in the mean expression characterized by the at least 1.5-fold change and FDR <  0.05 were identified. Subsequently, a two-step validation procedure was carried out. In the first step, a subset of selected population- differentiating transcripts was tested in the independent set of B-lymphocyte cell lines, using TLDA cards. Based on TLDA analysis, three transcripts representing Fch > 2 were chosen for validation. The differentiating status was confirmed for all of them: UTS2, UGT2B17 and SLC7A7. The mean expression of UTS2 was higher in CHB (25.8-fold change compared to CEU), while the expression of UGT2B17 and SLC7A7 was higher in CEU (3.2- and 2.2-fold change, respectively). In the next validation step, two transcripts were verified in the primary biological material. As an ultimate result of our study, two mRNA markers (UTS2 and UGT2B17) exhibiting population differences in the expression level in both B-cell line and in the blood were identified. Further statistical analysis confirmed the discriminatory potential of these two markers. CONCLUSIONS: An inter-population differences on the level of gene expression were identified in both B-cell lines and peripheral blood samples. These findings may have a practical application in the field of forensic science. In particular, these transcripts, targeted by specific probes, may be used as population-specific targets in the efforts aiming to separate mixture of blood from individuals of different populations. Notwithstanding, these results have to be confirmed on extended population group. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-018-0663-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-07 /pmc/articles/PMC6081795/ /pubmed/30086702 http://dx.doi.org/10.1186/s12863-018-0663-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Daca-Roszak, P.
Swierniak, M.
Jaksik, R.
Tyszkiewicz, T.
Oczko-Wojciechowska, M.
Zebracka-Gala, J.
Jarzab, B.
Witt, M.
Zietkiewicz, E.
Transcriptomic population markers for human population discrimination
title Transcriptomic population markers for human population discrimination
title_full Transcriptomic population markers for human population discrimination
title_fullStr Transcriptomic population markers for human population discrimination
title_full_unstemmed Transcriptomic population markers for human population discrimination
title_short Transcriptomic population markers for human population discrimination
title_sort transcriptomic population markers for human population discrimination
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081795/
https://www.ncbi.nlm.nih.gov/pubmed/30086702
http://dx.doi.org/10.1186/s12863-018-0663-2
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