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Dynamic Transcriptional and Epigenetic Regulation of Human Epidermal Keratinocyte Differentiation.


ABSTRACT: Human skin is maintained by the differentiation and maturation of interfollicular stem and progenitors cells. We used DeepCAGE, genome-wide profiling of histone modifications and retroviral integration analysis, to map transcripts, promoters, enhancers, and super-enhancers (SEs) in prospectively isolated keratinocytes and transit-amplifying progenitors, and retrospectively defined keratinocyte stem cells. We show that >95% of the active promoters are in common and differentially regulated in progenitors and differentiated keratinocytes, while approximately half of the enhancers and SEs are stage specific and account for most of the epigenetic changes occurring during differentiation. Transcription factor (TF) motif identification and correlation with TF binding site maps allowed the identification of TF circuitries acting on enhancers and SEs during differentiation. Overall, our study provides a broad, genome-wide description of chromatin dynamics and differential enhancer and promoter usage during epithelial differentiation, and describes a novel approach to identify active regulatory elements in rare stem cell populations.

SUBMITTER: Cavazza A 

PROVIDER: S-EPMC4834057 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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Dynamic Transcriptional and Epigenetic Regulation of Human Epidermal Keratinocyte Differentiation.

Cavazza Alessia A   Miccio Annarita A   Romano Oriana O   Petiti Luca L   Malagoli Tagliazucchi Guidantonio G   Peano Clelia C   Severgnini Marco M   Rizzi Ermanno E   De Bellis Gianluca G   Bicciato Silvio S   Mavilio Fulvio F  

Stem cell reports 20160331 4


Human skin is maintained by the differentiation and maturation of interfollicular stem and progenitors cells. We used DeepCAGE, genome-wide profiling of histone modifications and retroviral integration analysis, to map transcripts, promoters, enhancers, and super-enhancers (SEs) in prospectively isolated keratinocytes and transit-amplifying progenitors, and retrospectively defined keratinocyte stem cells. We show that >95% of the active promoters are in common and differentially regulated in pro  ...[more]

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