4.7 Review

Identification of non-coding silencer elements and their regulation of gene expression

Journal

NATURE REVIEWS MOLECULAR CELL BIOLOGY
Volume 24, Issue 6, Pages 383-395

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41580-022-00549-9

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Cell type- and differentiation-specific gene expression is controlled by genomic non-coding regulatory elements (NCREs), including promoters, enhancers, silencers, and insulators. Recent studies have focused on identifying and characterizing silencers, which repress gene transcription, and have highlighted their importance in homeostasis and disease. Understanding silencers has potential implications for genome research and therapeutic applications.
Cell type- and differentiation-specific gene expression is precisely controlled by genomic non-coding regulatory elements (NCREs), which include promoters, enhancers, silencers and insulators. It is estimated that more than 90% of disease-associated sequence variants lie within the non-coding part of the genome, potentially affecting the activity of NCREs. Consequently, the functional annotation of NCREs is a major driver of genome research. Compared with our knowledge of other regulatory elements, our knowledge of silencers, which are NCREs that repress the transcription of genes, is largely lacking. Multiple recent studies have reported large-scale identification of transcription silencer elements, indicating their importance in homeostasis and disease. In this Review, we discuss the biology of silencers, including methods for their discovery, epigenomic and other characteristics, and modes of function of silencers. We also discuss important silencer-relevant considerations in assessing data from genome-wide association studies and shed light on potential future silencer-based therapeutic applications. The genome contains various non-coding regulatory elements, including silencers of gene expression. Recent progress in the identification and characterization of silencers has considerably deepened our understanding of their function, and has shed light on the potential relevance of targeting silencers in therapy for hereditary diseases.

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