| Literature DB >> 33239788 |
Hongbo Yang1, Yu Luan1, Tingting Liu1, Hyung Joo Lee2, Li Fang3, Yanli Wang4, Xiaotao Wang1, Bo Zhang4, Qiushi Jin1, Khai Chung Ang5, Xiaoyun Xing2, Juan Wang1, Jie Xu1, Fan Song4, Iyyanki Sriranga1, Chachrit Khunsriraksakul4, Tarik Salameh4, Daofeng Li2, Mayank N K Choudhary2, Jacek Topczewski6,7, Kai Wang3, Glenn S Gerhard8, Ross C Hardison9, Ting Wang2, Keith C Cheng5, Feng Yue10,11.
Abstract
The zebrafish (Danio rerio) has been widely used in the study of human disease and development, and about 70% of the protein-coding genes are conserved between the two species1. However, studies in zebrafish remain constrained by the sparse annotation of functional control elements in the zebrafish genome. Here we performed RNA sequencing, assay for transposase-accessible chromatin using sequencing (ATAC-seq), chromatin immunoprecipitation with sequencing, whole-genome bisulfite sequencing, and chromosome conformation capture (Hi-C) experiments in up to eleven adult and two embryonic tissues to generate a comprehensive map of transcriptomes, cis-regulatory elements, heterochromatin, methylomes and 3D genome organization in the zebrafish Tübingen reference strain. A comparison of zebrafish, human and mouse regulatory elements enabled the identification of both evolutionarily conserved and species-specific regulatory sequences and networks. We observed enrichment of evolutionary breakpoints at topologically associating domain boundaries, which were correlated with strong histone H3 lysine 4 trimethylation (H3K4me3) and CCCTC-binding factor (CTCF) signals. We performed single-cell ATAC-seq in zebrafish brain, which delineated 25 different clusters of cell types. By combining long-read DNA sequencing and Hi-C, we assembled the sex-determining chromosome 4 de novo. Overall, our work provides an additional epigenomic anchor for the functional annotation of vertebrate genomes and the study of evolutionarily conserved elements of 3D genome organization.Entities:
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Year: 2020 PMID: 33239788 PMCID: PMC8183574 DOI: 10.1038/s41586-020-2962-9
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962