Back to Search
Start Over
The characteristics of CTCF binding sequences contribute to enhancer blocking activity.
- Source :
-
Nucleic acids research [Nucleic Acids Res] 2024 Sep 23; Vol. 52 (17), pp. 10180-10193. - Publication Year :
- 2024
-
Abstract
- While the elements encoding enhancers and promoters have been relatively well studied, the full spectrum of insulator elements which bind the CCCTC binding factor (CTCF), is relatively poorly characterized. This is partly due to the genomic context of CTCF sites greatly influencing their roles and activity. Here we have developed an experimental system to determine the ability of minimal, consistently sized, individual CTCF elements to interpose between enhancers and promoters and thereby reduce gene expression during differentiation. Importantly, each element is tested in the identical location thereby minimising the effect of genomic context. We found no correlation between the ability of CTCF elements to block enhancer-promoter activity with the degree of evolutionary conservation; their resemblance to the consensus core sequences; or the number of CTCF core motifs harboured in the element. Nevertheless, we have shown that the strongest enhancer-promoter blockers include a previously described bound element lying upstream of the CTCF core motif. In addition, we found other uncharacterised DNaseI footprints located close to the core motif that may affect function. We have developed an assay of CTCF sequences which will enable researchers to sub-classify individual CTCF elements in a uniform and unbiased way.<br /> (© The Author(s) 2024. Published by Oxford University Press on behalf of Nucleic Acids Research.)
- Subjects :
- Binding Sites genetics
Humans
Animals
Mice
Repressor Proteins metabolism
Repressor Proteins genetics
Insulator Elements genetics
Protein Binding
Nucleotide Motifs
Cell Line
Gene Expression Regulation
Cell Differentiation genetics
CCCTC-Binding Factor metabolism
CCCTC-Binding Factor genetics
Enhancer Elements, Genetic
Promoter Regions, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 1362-4962
- Volume :
- 52
- Issue :
- 17
- Database :
- MEDLINE
- Journal :
- Nucleic acids research
- Publication Type :
- Academic Journal
- Accession number :
- 39106157
- Full Text :
- https://doi.org/10.1093/nar/gkae666