CTCF knockout in zebrafish induces alterations in regulatory landscapes and developmental gene expression

Abstract

CTCF is an 11-zinc-finger DNA-binding protein that acts as a transcriptional repressor and insulator as well as an architectural protein required for 3D genome folding. CTCF mediates long-range chromatin looping and is enriched at the boundaries of topologically associating domains, which are sub-megabase chromatin structures that are believed to facilitate enhancer-promoter interactions within regulatory landscapes. Although CTCF is essential for cycling cells and developing embryos, its in vitro removal has only modest effects over gene expression, challenging the concept that CTCF-mediated chromatin interactions and topologically associated domains are a fundamental requirement for gene regulation. Here we link the loss of chromatin structure and gene regulation in an in vivo model and during animal development. We generated a ctcf knockout mutant in zebrafish that allows us to monitor the effect of CTCF loss of function during embryo patterning and organogenesis. CTCF absence leads to loss of chromatin structure in zebrafish embryos and affects the expression of thousands of genes, including many developmental genes. In addition, chromatin accessibility, both at CTCF binding sites and cis-regulatory elements, is severely compromised in ctcf mutants. Probing chromatin interactions from developmental genes at high resolution, we further demonstrate that promoters fail to fully establish long-range contacts with their associated regulatory landscapes, leading to altered gene expression patterns and disruption of developmental programs. Our results demonstrate that CTCF and topologically associating domains are essential to regulate gene expression during embryonic development, providing the structural basis for the establishment of developmental gene regulatory landscapes.

Topologically Associating Domains and Regulatory Landscapes in Development, Evolution and Disease

“…In this sense, the acute depletion of cohesin or CTCF in mammalian cells shows only a moderate effect in gene expression, affecting from some hundreds to few thousands of genes in different systems ( Nora et al, 2017 ; Rao et al, 2017 ; Kubo et al, 2021 ). These studies have been limited in vivo due to the essential nature of cohesin and CTCF ( Moore et al, 2012 ; Ju et al, 2013 ); however, this limitation was recently overcome by generating zebrafish ctcf knock-out embryos ( Franke et al, 2020 ). In these embryos, a prolonged maternal contribution allows the survival of the mutant embryos until larval stages, when the absence of CTCF results in the miss-regulation of thousands of genes enriched in developmental functions ( Franke et al, 2020 ).…”

“…These studies have been limited in vivo due to the essential nature of cohesin and CTCF ( Moore et al, 2012 ; Ju et al, 2013 ); however, this limitation was recently overcome by generating zebrafish ctcf knock-out embryos ( Franke et al, 2020 ). In these embryos, a prolonged maternal contribution allows the survival of the mutant embryos until larval stages, when the absence of CTCF results in the miss-regulation of thousands of genes enriched in developmental functions ( Franke et al, 2020 ). Although part of the effects seen in CTCF depletion or knock-out approaches may be indirect due to CTCF function as a TF, a subset of chromatin interactions involving lineage-specific genes change upon CTCF loss ( Kubo et al, 2021 ).…”

Virtual meeting, real and sound science: report of the 17th Meeting of the Spanish Society for Developmental Biology (SEBD-2020)

“…Finally, the four flash talks by Lorena Buono (Andalusian Centre for Developmental Biology), Jose M. Santos-Pereira (Andalusian Centre for Developmental Biology), Sandra Acosta (Institut de Biologia Evolutiva, CSIC-Universitat Pompeu Fabra) and Tore Bleckwehl (Center for Molecular Medicine Cologne, University of Cologne). In their talks, they discussed gene network bifurcation between the neural retina and retinal pigmented epithelium during optic cup morphogenesis (Buono et al, 2020), the role of CTCF controlling chromatin organization during development using a zebrafish knockout model (Franke et al, 2020), tissue-specific functions of intronic enhancers (Borsari et al, 2020), and the importance of H3K4me1, and enhancer priming for germline competence (Bleckwehl et al, 2020), respectively.…”