4.8 Article

Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation

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NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-019-09828-0

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资金

  1. ICGC Breast Cancer Working group by the Breast Cancer Somatic Genetics Study (BASIS), a European research project - European Community's Seventh Framework Program (FP7/2010-2014) [242006]
  2. Triple Negative project - Wellcome Trust [077012/Z/05/Z]
  3. Dutch Cancer Foundation (KWF) [KUN 2013-5833]
  4. CRUK Advanced Clinician Scientist Award [C60100/A23916]
  5. EU-FP7-DDR response project
  6. J. Robert Oppen-heimer Fellowship at Los Alamos National Laboratory
  7. Dana-Farber/Harvard Cancer Center SPORE in Breast Cancer [NIH/NCI 5 P50 CA168504-02]
  8. ERC Advanced Grant [ERC-2012-AdG-322737]
  9. ERC Proof-of-Concept Grant [ERC-2017-PoC-767854]
  10. Cancer Genomics Netherlands (CGC.nl) through a grant from the Netherlands Organization of Scientific research (NWO)
  11. Dutch national e-infrastructure (SURF Foundation)

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Global loss of DNA methylation and CpG island (CGI) hypermethylation are key epigenomic aberrations in cancer. Global loss manifests itself in partially methylated domains (PMDs) which extend up to megabases. However, the distribution of PMDs within and between tumor types, and their effects on key functional genomic elements including CGIs are poorly defined. We comprehensively show that loss of methylation in PMDs occurs in a large fraction of the genome and represents the prime source of DNA methylation variation. PMDs are hypervariable in methylation level, size and distribution, and display elevated mutation rates. They impose intermediate DNA methylation levels incognizant of functional genomic elements including CGIs, underpinning a CGI methylator phenotype (CIMP). Repression effects on tumor suppressor genes are negligible as they are generally excluded from PMDs. The genomic distribution of PMDs reports tissue-of-origin and may represent tissue-specific silent regions which tolerate instability at the epigenetic, transcriptomic and genetic level.

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