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A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2
OBJECTIVE: Alu elements are retroposons that invaded the primate genome and shaped its biology. Some Alus inserted recently and are polymorphic in the human population. It is these Alus that are being sought after in disease association studies and regulatory biology. Discovering polymorphic Alus in...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458609/ https://www.ncbi.nlm.nih.gov/pubmed/30975199 http://dx.doi.org/10.1186/s13104-019-4247-7 |
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author | Hamdi, Hamdi K. Reddy, Siddana Laz, Nada Eltaher, Renad Kandell, Zahraa Mahmud, Teif Alenazi, Lamia Haroun, Basheer Hassan, Mohanad Ragavendra, Raju |
author_facet | Hamdi, Hamdi K. Reddy, Siddana Laz, Nada Eltaher, Renad Kandell, Zahraa Mahmud, Teif Alenazi, Lamia Haroun, Basheer Hassan, Mohanad Ragavendra, Raju |
author_sort | Hamdi, Hamdi K. |
collection | PubMed |
description | OBJECTIVE: Alu elements are retroposons that invaded the primate genome and shaped its biology. Some Alus inserted recently and are polymorphic in the human population. It is these Alus that are being sought after in disease association studies and regulatory biology. Discovering polymorphic Alus in the human genome can open areas of new research in these fields. RESULTS: Using the polymerase chain reaction on genomic DNA, we identified a polymorphic Alu in the flanking region of the TFAP2B and TFAP2D genes. The new insert was found in higher frequency in Europeans (0.4) and Asians (0.38) and lower frequency in Africans (0.25). We also show this Alu to be part of a 3 Alu cassette that is human specific. The TFAP2B and TFAP2D genes encode members of the transcription factor AP-2, which plays a role in organ development. The insertion of this Alu cassette flanking the transcription factor genes distinguishes humans from the primates. This cassette can possibly affect the regulation of both genes or alternately provoke genomic deletions, which we have shown in this study. Its presence in such a location is intriguing and unquestionably opens an investigational window in disease association studies and in the field of gene regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-019-4247-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6458609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64586092019-04-19 A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2 Hamdi, Hamdi K. Reddy, Siddana Laz, Nada Eltaher, Renad Kandell, Zahraa Mahmud, Teif Alenazi, Lamia Haroun, Basheer Hassan, Mohanad Ragavendra, Raju BMC Res Notes Research Note OBJECTIVE: Alu elements are retroposons that invaded the primate genome and shaped its biology. Some Alus inserted recently and are polymorphic in the human population. It is these Alus that are being sought after in disease association studies and regulatory biology. Discovering polymorphic Alus in the human genome can open areas of new research in these fields. RESULTS: Using the polymerase chain reaction on genomic DNA, we identified a polymorphic Alu in the flanking region of the TFAP2B and TFAP2D genes. The new insert was found in higher frequency in Europeans (0.4) and Asians (0.38) and lower frequency in Africans (0.25). We also show this Alu to be part of a 3 Alu cassette that is human specific. The TFAP2B and TFAP2D genes encode members of the transcription factor AP-2, which plays a role in organ development. The insertion of this Alu cassette flanking the transcription factor genes distinguishes humans from the primates. This cassette can possibly affect the regulation of both genes or alternately provoke genomic deletions, which we have shown in this study. Its presence in such a location is intriguing and unquestionably opens an investigational window in disease association studies and in the field of gene regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-019-4247-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-11 /pmc/articles/PMC6458609/ /pubmed/30975199 http://dx.doi.org/10.1186/s13104-019-4247-7 Text en © The Author(s) 2019 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 Note Hamdi, Hamdi K. Reddy, Siddana Laz, Nada Eltaher, Renad Kandell, Zahraa Mahmud, Teif Alenazi, Lamia Haroun, Basheer Hassan, Mohanad Ragavendra, Raju A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2 |
title | A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2 |
title_full | A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2 |
title_fullStr | A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2 |
title_full_unstemmed | A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2 |
title_short | A human specific Alu DNA cassette is found flanking the genes of transcription factor AP2 |
title_sort | human specific alu dna cassette is found flanking the genes of transcription factor ap2 |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458609/ https://www.ncbi.nlm.nih.gov/pubmed/30975199 http://dx.doi.org/10.1186/s13104-019-4247-7 |
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