Mapping chromatin accessibility and active regulatory elements reveals pathological mechanisms in human gliomas.
Karolina StępniakMagdalena A MachnickaJakub MieczkowskiAnna MacioszekBartosz WojtaśBartłomiej GielniewskiKatarzyna PoleszakMalgorzata PeryczSylwia K KrólRafał GuzikMichał J DąbrowskiMichał DramińskiMarta JardanowskaIlona GrabowiczAgata DziedzicHanna KranasKarolina SienkiewiczKlev DiamantiKatarzyna KotulskaWiesława GrajkowskaMarcin RoszkowskiTomasz CzernickiAndrzej MarchelJan KomorowskiBozena KaminskaBartek WilczyńskiPublished in: Nature communications (2021)
Chromatin structure and accessibility, and combinatorial binding of transcription factors to regulatory elements in genomic DNA control transcription. Genetic variations in genes encoding histones, epigenetics-related enzymes or modifiers affect chromatin structure/dynamics and result in alterations in gene expression contributing to cancer development or progression. Gliomas are brain tumors frequently associated with epigenetics-related gene deregulation. We perform whole-genome mapping of chromatin accessibility, histone modifications, DNA methylation patterns and transcriptome analysis simultaneously in multiple tumor samples to unravel epigenetic dysfunctions driving gliomagenesis. Based on the results of the integrative analysis of the acquired profiles, we create an atlas of active enhancers and promoters in benign and malignant gliomas. We explore these elements and intersect with Hi-C data to uncover molecular mechanisms instructing gene expression in gliomas.
Keyphrases
- dna methylation
- genome wide
- gene expression
- transcription factor
- high grade
- copy number
- genome wide identification
- dna binding
- high resolution
- endothelial cells
- squamous cell carcinoma
- dna damage
- cell free
- mass spectrometry
- circulating tumor
- young adults
- squamous cell
- binding protein
- childhood cancer
- network analysis
- bioinformatics analysis