Circular ecDNA promotes accessible chromatin and high oncogene expression.
Journal
Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
received:
06
11
2018
accepted:
26
09
2019
pubmed:
22
11
2019
medline:
14
4
2020
entrez:
22
11
2019
Statut:
ppublish
Résumé
Oncogenes are commonly amplified on particles of extrachromosomal DNA (ecDNA) in cancer
Identifiants
pubmed: 31748743
doi: 10.1038/s41586-019-1763-5
pii: 10.1038/s41586-019-1763-5
pmc: PMC7094777
mid: NIHMS1065820
doi:
Substances chimiques
Chromatin
0
DNA, Circular
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
699-703Subventions
Organisme : NHGRI NIH HHS
ID : RM1 HG007735
Pays : United States
Organisme : NINDS NIH HHS
ID : P30 NS047101
Pays : United States
Organisme : Howard Hughes Medical Institute
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS073831
Pays : United States
Organisme : NIH HHS
ID : NS73831
Pays : United States
Organisme : NIH HHS
ID : GM114362
Pays : United States
Organisme : NHGRI NIH HHS
ID : P50 HG007735
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS080939
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA209919
Pays : United States
Organisme : NIH HHS
ID : S10 OD023527
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM114362
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM065490
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA067754
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009523
Pays : United States
Références
Turner, K. M. et al. Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity. Nature 543, 122–125 (2017).
doi: 10.1038/nature21356
Verhaak, R. G. W., Bafna, V. & Mischel, P. S. Extrachromosomal oncogene amplification in tumour pathogenesis and evolution. Nat. Rev. Cancer 19, 283–288 (2019).
doi: 10.1038/s41568-019-0128-6
Gibcus, J. H. & Dekker, J. The hierarchy of the 3D genome. Mol. Cell 49, 773–782 (2013).
doi: 10.1016/j.molcel.2013.02.011
Dixon, J. R., Gorkin, D. U. & Ren, B. Chromatin domains: the unit of chromosome organization. Mol. Cell 62, 668–680 (2016).
doi: 10.1016/j.molcel.2016.05.018
Corces, M. R. et al. The chromatin accessibility landscape of primary human cancers. Science 362, eaav1898 (2018).
doi: 10.1126/science.aav1898
Hnisz, D. et al. Activation of proto-oncogenes by disruption of chromosome neighborhoods. Science 351, 1454–1458 (2016).
doi: 10.1126/science.aad9024
Møller, H. D. et al. Circular DNA elements of chromosomal origin are common in healthy human somatic tissue. Nat. Commun. 9, 1069 (2018).
doi: 10.1038/s41467-018-03369-8
Shibata, Y. et al. Extrachromosomal microDNAs and chromosomal microdeletions in normal tissues. Science 336, 82–86 (2012).
doi: 10.1126/science.1213307
Deshpande, V. et al. Exploring the landscape of focal amplifications in cancer using AmpliconArchitect. Nat. Commun. 10, 392 (2019).
doi: 10.1038/s41467-018-08200-y
Mendelowitz, L. & Pop, M. Computational methods for optical mapping. Gigascience 3, 33 (2014).
doi: 10.1186/2047-217X-3-33
Mak, A. C. et al. Genome-wide structural variation detection by genome mapping on nanochannel arrays. Genetics 202, 351–362 (2016).
doi: 10.1534/genetics.115.183483
Demmerle, J. et al. Strategic and practical guidelines for successful structured illumination microscopy. Nat. Protocols 12, 988–1010 (2017).
doi: 10.1038/nprot.2017.019
Schimke, R. T. Gene amplification in cultured animal cells. Cell 37, 705–713 (1984).
doi: 10.1016/0092-8674(84)90406-9
Storlazzi, C. T. et al. Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure. Genome Res. 20, 1198–1206 (2010).
doi: 10.1101/gr.106252.110
L’Abbate, A. et al. MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences. Leukemia 32, 2152–2166 (2018).
doi: 10.1038/s41375-018-0033-0
Baylin, S. B. & Jones, P. A. Epigenetic determinants of cancer. Cold Spring Harb. Perspect. Biol. 8, a019505 (2016).
doi: 10.1101/cshperspect.a019505
Lee, D. Y., Hayes, J. J., Pruss, D. & Wolffe, A. P. A positive role for histone acetylation in transcription factor access to nucleosomal DNA. Cell 72, 73–84 (1993).
doi: 10.1016/0092-8674(93)90051-Q
Luger, K., Mäder, A. W., Richmond, R. K., Sargent, D. F. & Richmond, T. J. Crystal structure of the nucleosome core particle at 2.8 A resolution. Nature 389, 251–260 (1997).
doi: 10.1038/38444
Smith, G. et al. c-Myc-induced extrachromosomal elements carry active chromatin. Neoplasia 5, 110–120 (2003).
doi: 10.1016/S1476-5586(03)80002-7
Chen, X. et al. ATAC-see reveals the accessible genome by transposase-mediated imaging and sequencing. Nat. Methods 13, 1013–1020 (2016).
doi: 10.1038/nmeth.4031
Solovei, I. et al. Topology of double minutes (dmins) and homogeneously staining regions (HSRs) in nuclei of human neuroblastoma cell lines. Genes Chromosom. Cancer 29, 297–308 (2000).
doi: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1046>3.0.CO;2-H
Fang, R. et al. Mapping of long-range chromatin interactions by proximity ligation-assisted ChIP-seq. Cell Res. 26, 1345–1348 (2016).
doi: 10.1038/cr.2016.137
Mumbach, M. R. et al. HiChIP: efficient and sensitive analysis of protein-directed genome architecture. Nat. Methods 13, 919–922 (2016).
doi: 10.1038/nmeth.3999
Rowley, M. J. & Corces, V. G. Organizational principles of 3D genome architecture. Nat. Rev. Genet. 19, 789–800 (2018).
doi: 10.1038/s41576-018-0060-8
Bailey, M. H. et al. Comprehensive characterization of cancer driver genes and mutations. Cell 173, 371–385.e318 (2018).
doi: 10.1016/j.cell.2018.02.060
deCarvalho, A. C. et al. Discordant inheritance of chromosomal and extrachromosomal DNA elements contributes to dynamic disease evolution in glioblastoma. Nat. Genet. 50, 708–717 (2018).
doi: 10.1038/s41588-018-0105-0
Lederberg, J. Cell genetics and hereditary symbiosis. Physiol. Rev. 32, 403–430 (1952).
doi: 10.1152/physrev.1952.32.4.403
Nathanson, D. A. et al. Targeted therapy resistance mediated by dynamic regulation of extrachromosomal mutant EGFR DNA. Science 343, 72–76 (2014).
doi: 10.1126/science.1241328
McGranahan, N. & Swanton, C. Clonal heterogeneity and tumor evolution: past, present, and the future. Cell 168, 613–628 (2017).
doi: 10.1016/j.cell.2017.01.018
Xu, K. et al. Structure and evolution of double minutes in diagnosis and relapse brain tumors. Acta Neuropathol. 137, 123–137 (2019).
doi: 10.1007/s00401-018-1912-1
Cao, H. et al. Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology. Gigascience 3, 34 (2014).
doi: 10.1186/2047-217X-3-34
Corces, M. R. et al. An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues. Nat. Methods 14, 959–962 (2017).
doi: 10.1038/nmeth.4396
Juric, I. et al. MAPS: model-based analysis of long-range chromatin interactions from PLAC-seq and HiChIP experiments. PLOS Comput. Biol. 15, e1006982 (2019).
doi: 10.1371/journal.pcbi.1006982
Raviram, R. et al. 4C-ker: a method to reproducibly identify genome-wide interactions captured by 4C-seq experiments. PLOS Comput. Biol. 12, e1004780 (2016).
doi: 10.1371/journal.pcbi.1004780
Thakore, P. I. et al. Highly specific epigenome editing by CRISPR-Cas9 repressors for silencing of distal regulatory elements. Nat. Methods 12, 1143–1149 (2015).
doi: 10.1038/nmeth.3630