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A map of mobile DNA insertions in the NCI-60 human cancer cell panel
BACKGROUND: The National Cancer Institute-60 (NCI-60) cell lines are among the most widely used models of human cancer. They provide a platform to integrate DNA sequence information, epigenetic data, RNA and protein expression, and pharmacologic susceptibilities in studies of cancer cell biology. Ge...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087121/ https://www.ncbi.nlm.nih.gov/pubmed/27807467 http://dx.doi.org/10.1186/s13100-016-0078-4 |
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author | Zampella, John G. Rodić, Nemanja Yang, Wan Rou Huang, Cheng Ran Lisa Welch, Jane Gnanakkan, Veena P. Cornish, Toby C. Boeke, Jef D. Burns, Kathleen H. |
author_facet | Zampella, John G. Rodić, Nemanja Yang, Wan Rou Huang, Cheng Ran Lisa Welch, Jane Gnanakkan, Veena P. Cornish, Toby C. Boeke, Jef D. Burns, Kathleen H. |
author_sort | Zampella, John G. |
collection | PubMed |
description | BACKGROUND: The National Cancer Institute-60 (NCI-60) cell lines are among the most widely used models of human cancer. They provide a platform to integrate DNA sequence information, epigenetic data, RNA and protein expression, and pharmacologic susceptibilities in studies of cancer cell biology. Genome-wide studies of the complete panel have included exome sequencing, karyotyping, and copy number analyses but have not targeted repetitive sequences. Interspersed repeats derived from mobile DNAs are a significant source of heritable genetic variation, and insertions of active elements can occur somatically in malignancy. METHOD: We used Transposon Insertion Profiling by microarray (TIP-chip) to map Long INterspersed Element-1 (LINE-1, L1) and Alu Short INterspersed Element (SINE) insertions in cancer genes in NCI-60 cells. We focused this discovery effort on annotated Cancer Gene Index loci. RESULTS: We catalogued a total of 749 and 2,100 loci corresponding to candidate LINE-1 and Alu insertion sites, respectively. As expected, these numbers encompass previously known insertions, polymorphisms shared in unrelated tumor cell lines, as well as unique, potentially tumor-specific insertions. We also conducted association analyses relating individual insertions to a variety of cellular phenotypes. CONCLUSIONS: These data provide a resource for investigators with interests in specific cancer gene loci or mobile element insertion effects more broadly. Our data underscore that significant genetic variation in cancer genomes is owed to LINE-1 and Alu retrotransposons. Our findings also indicate that as large numbers of cancer genomes become available, it will be possible to associate individual transposable element insertion variants with molecular and phenotypic features of these malignancies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13100-016-0078-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5087121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50871212016-11-02 A map of mobile DNA insertions in the NCI-60 human cancer cell panel Zampella, John G. Rodić, Nemanja Yang, Wan Rou Huang, Cheng Ran Lisa Welch, Jane Gnanakkan, Veena P. Cornish, Toby C. Boeke, Jef D. Burns, Kathleen H. Mob DNA Research BACKGROUND: The National Cancer Institute-60 (NCI-60) cell lines are among the most widely used models of human cancer. They provide a platform to integrate DNA sequence information, epigenetic data, RNA and protein expression, and pharmacologic susceptibilities in studies of cancer cell biology. Genome-wide studies of the complete panel have included exome sequencing, karyotyping, and copy number analyses but have not targeted repetitive sequences. Interspersed repeats derived from mobile DNAs are a significant source of heritable genetic variation, and insertions of active elements can occur somatically in malignancy. METHOD: We used Transposon Insertion Profiling by microarray (TIP-chip) to map Long INterspersed Element-1 (LINE-1, L1) and Alu Short INterspersed Element (SINE) insertions in cancer genes in NCI-60 cells. We focused this discovery effort on annotated Cancer Gene Index loci. RESULTS: We catalogued a total of 749 and 2,100 loci corresponding to candidate LINE-1 and Alu insertion sites, respectively. As expected, these numbers encompass previously known insertions, polymorphisms shared in unrelated tumor cell lines, as well as unique, potentially tumor-specific insertions. We also conducted association analyses relating individual insertions to a variety of cellular phenotypes. CONCLUSIONS: These data provide a resource for investigators with interests in specific cancer gene loci or mobile element insertion effects more broadly. Our data underscore that significant genetic variation in cancer genomes is owed to LINE-1 and Alu retrotransposons. Our findings also indicate that as large numbers of cancer genomes become available, it will be possible to associate individual transposable element insertion variants with molecular and phenotypic features of these malignancies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13100-016-0078-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-31 /pmc/articles/PMC5087121/ /pubmed/27807467 http://dx.doi.org/10.1186/s13100-016-0078-4 Text en © The Author(s). 2016 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 Zampella, John G. Rodić, Nemanja Yang, Wan Rou Huang, Cheng Ran Lisa Welch, Jane Gnanakkan, Veena P. Cornish, Toby C. Boeke, Jef D. Burns, Kathleen H. A map of mobile DNA insertions in the NCI-60 human cancer cell panel |
title | A map of mobile DNA insertions in the NCI-60 human cancer cell panel |
title_full | A map of mobile DNA insertions in the NCI-60 human cancer cell panel |
title_fullStr | A map of mobile DNA insertions in the NCI-60 human cancer cell panel |
title_full_unstemmed | A map of mobile DNA insertions in the NCI-60 human cancer cell panel |
title_short | A map of mobile DNA insertions in the NCI-60 human cancer cell panel |
title_sort | map of mobile dna insertions in the nci-60 human cancer cell panel |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087121/ https://www.ncbi.nlm.nih.gov/pubmed/27807467 http://dx.doi.org/10.1186/s13100-016-0078-4 |
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