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High-throughput characterization of the role of non-B DNA motifs on promoter function

Alternative DNA conformations, termed non-B DNA structures, can affect transcription, but the underlying mechanisms and their functional impact have not been systematically characterized. Here, we used computational genomic analyses coupled with massively parallel reporter assays (MPRAs) to show tha...

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Detalles Bibliográficos
Autores principales: Georgakopoulos-Soares, Ilias, Victorino, Jesus, Parada, Guillermo E., Agarwal, Vikram, Zhao, Jingjing, Wong, Hei Yuen, Umar, Mubarak Ishaq, Elor, Orry, Muhwezi, Allan, An, Joon-Yong, Sanders, Stephan J., Kwok, Chun Kit, Inoue, Fumitaka, Hemberg, Martin, Ahituv, Nadav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105345/
https://www.ncbi.nlm.nih.gov/pubmed/35573091
http://dx.doi.org/10.1016/j.xgen.2022.100111
Descripción
Sumario:Alternative DNA conformations, termed non-B DNA structures, can affect transcription, but the underlying mechanisms and their functional impact have not been systematically characterized. Here, we used computational genomic analyses coupled with massively parallel reporter assays (MPRAs) to show that certain non-B DNA structures have a substantial effect on gene expression. Genomic analyses found that non-B DNA structures at promoters harbor an excess of germline variants. Analysis of multiple MPRAs, including a promoter library specifically designed to perturb non-B DNA structures, functionally validated that Z-DNA can significantly affect promoter activity. We also observed that biophysical properties of non-B DNA motifs, such as the length of Z-DNA motifs and the orientation of G-quadruplex structures relative to transcriptional direction, have a significant effect on promoter activity. Combined, their higher mutation rate and functional effect on transcription implicate a subset of non-B DNA motifs as major drivers of human gene-expression-associated phenotypes.