Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
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
_version_ 1782463856526753792
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
work_keys_str_mv AT zampellajohng amapofmobilednainsertionsinthenci60humancancercellpanel
AT rodicnemanja amapofmobilednainsertionsinthenci60humancancercellpanel
AT yangwanrou amapofmobilednainsertionsinthenci60humancancercellpanel
AT huangchengranlisa amapofmobilednainsertionsinthenci60humancancercellpanel
AT welchjane amapofmobilednainsertionsinthenci60humancancercellpanel
AT gnanakkanveenap amapofmobilednainsertionsinthenci60humancancercellpanel
AT cornishtobyc amapofmobilednainsertionsinthenci60humancancercellpanel
AT boekejefd amapofmobilednainsertionsinthenci60humancancercellpanel
AT burnskathleenh amapofmobilednainsertionsinthenci60humancancercellpanel
AT zampellajohng mapofmobilednainsertionsinthenci60humancancercellpanel
AT rodicnemanja mapofmobilednainsertionsinthenci60humancancercellpanel
AT yangwanrou mapofmobilednainsertionsinthenci60humancancercellpanel
AT huangchengranlisa mapofmobilednainsertionsinthenci60humancancercellpanel
AT welchjane mapofmobilednainsertionsinthenci60humancancercellpanel
AT gnanakkanveenap mapofmobilednainsertionsinthenci60humancancercellpanel
AT cornishtobyc mapofmobilednainsertionsinthenci60humancancercellpanel
AT boekejefd mapofmobilednainsertionsinthenci60humancancercellpanel
AT burnskathleenh mapofmobilednainsertionsinthenci60humancancercellpanel