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DNA binding domain undergoes dynamic and selective protein–protein interactions to facilitate CTCF insulation

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SUMMARY CTCF is required for three-dimensional chromatin organization and a predominant insulator protein. However, its roles in insulating enhancers have not been fully explained in 3D nuclear organization. Here, we found that the CTCF DNA binding domain (DBD) forms dynamic self-interacting clusters. We next investigated the spatial relationships between these clusters and other transcription regulators with a light-induced imaging system. Strikingly, CTCF DBD clusters were found to incorporate other insulator proteins but are not coenriched with transcriptional activators in the nucleus. This property is not observed in other domains of CTCF or the DBDs of other transcription factors. Moreover, endogenous CTCF shows a phenotype consistent with the DBD by forming small protein clusters and interacts less transcriptional activators bound, CTCF motif arrays. Our results reveal an interesting phenomenon that CTCF DBD interacts with insulator proteins and selectively localizes to nuclear positions with lower concentrations of transcriptional activators, providing new insights into the insulation function of CTCF.
Title: DNA binding domain undergoes dynamic and selective protein–protein interactions to facilitate CTCF insulation
Description:
SUMMARY CTCF is required for three-dimensional chromatin organization and a predominant insulator protein.
However, its roles in insulating enhancers have not been fully explained in 3D nuclear organization.
Here, we found that the CTCF DNA binding domain (DBD) forms dynamic self-interacting clusters.
We next investigated the spatial relationships between these clusters and other transcription regulators with a light-induced imaging system.
Strikingly, CTCF DBD clusters were found to incorporate other insulator proteins but are not coenriched with transcriptional activators in the nucleus.
This property is not observed in other domains of CTCF or the DBDs of other transcription factors.
Moreover, endogenous CTCF shows a phenotype consistent with the DBD by forming small protein clusters and interacts less transcriptional activators bound, CTCF motif arrays.
Our results reveal an interesting phenomenon that CTCF DBD interacts with insulator proteins and selectively localizes to nuclear positions with lower concentrations of transcriptional activators, providing new insights into the insulation function of CTCF.

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