Cornelia de Lange syndrome mutations in NIPBL can impair cohesin-mediated DNA loop extrusion.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 35476527.
- Also identified by DOI 10.1073/pnas.2201029119 and PMC identifier 9170158.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Cornelia de Lange syndrome (CdLS) is a developmental multisystem disorder frequently associated with mutations in NIPBL. CdLS is thought to arise from developmental gene regulation defects, but how NIPBL mutations cause these is unknown. Here we show that several NIPBL mutations impair the DNA loop extrusion activity of cohesin. Because this activity is required for the formation of chromatin loops and topologically associating domains, which have important roles in gene regulation, our results suggest that defects in cohesin-mediated loop extrusion contribute to the etiology of CdLS by altering interactions between developmental genes and their enhancers.
Medical subject headings
- De Lange Syndrome