TY - JOUR
T1 - A map of cis-regulatory elements and 3D genome structures in zebrafish
AU - Yang, Hongbo
AU - Luan, Yu
AU - Liu, Tingting
AU - Lee, Hyung Joo
AU - Fang, Li
AU - Wang, Yanli
AU - Wang, Xiaotao
AU - Zhang, Bo
AU - Jin, Qiushi
AU - Ang, Khai Chung
AU - Xing, Xiaoyun
AU - Wang, Juan
AU - Xu, Jie
AU - Song, Fan
AU - Sriranga, Iyyanki
AU - Khunsriraksakul, Chachrit
AU - Salameh, Tarik
AU - Li, Daofeng
AU - Choudhary, Mayank N.K.
AU - Topczewski, Jacek
AU - Wang, Kai
AU - Gerhard, Glenn S.
AU - Hardison, Ross C.
AU - Wang, Ting
AU - Cheng, Keith C.
AU - Yue, Feng
N1 - Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/12/10
Y1 - 2020/12/10
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85096586201&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85096586201&partnerID=8YFLogxK
U2 - 10.1038/s41586-020-2962-9
DO - 10.1038/s41586-020-2962-9
M3 - Article
C2 - 33239788
AN - SCOPUS:85096586201
SN - 0028-0836
VL - 588
SP - 337
EP - 343
JO - Nature
JF - Nature
IS - 7837
ER -