Abstract
BackgroundThe CTCF insulator protein is a highly conserved zinc finger protein that has been implicated in many aspects of gene regulation and nuclear organization. The protein has been hypothesized to organize the human genome by forming DNA loops.ResultsIn this paper, we report biochemical evidence to support the role for CTCF in forming DNA loops. We have measured DNA bending by CTCF at the chicken HS4 β-globin FII insulator element in vitro and have observed a unique DNA structure with aberrant electrophoretic mobility which we believe to be a DNA loop. CTCF is able to form this unusual DNA structure at two other binding sites: the c-myc P2 promoter and the chicken F1 lysozyme gene silencer. We also demonstrate that the length though not the sequence of the DNA downstream of the binding site is important for the ability of CTCF to form this unusual DNA structure. We hypothesize that a single CTCF protein molecule is able to act as a "looper" possibly through the use of several of its zinc fingers.ConclusionsCTCF is able to form an unusual DNA structure through the zinc finger domain of the protein. This unusual DNA structure is formed in a directional manner by the CTCF protein. The findings described in this paper suggest mechanisms by which CTCF is able to form DNA loops, organize the mammalian genome and function as an insulator protein.
Highlights
The CTCF insulator protein is a highly conserved zinc finger protein that has been implicated in many aspects of gene regulation and nuclear organization
SUMOylation had no effect on CTCF’s ability to bend DNA, we found that the CTCF protein does not act as a typical DNA bending protein
We find that the SUMOylation of CTCF does not affect its ability to form this unusual DNA structure
Summary
The CTCF insulator protein is a highly conserved zinc finger protein that has been implicated in many aspects of gene regulation and nuclear organization. The CTCF protein has a central zinc finger domain that shows 100% amino acid conservation between the chicken form and the human form of the protein. This central zinc finger domain is flanked by an NH2-terminal domain and a carboxy-terminal domain, both of which have an unknown structure. These binding studies were performed by deleting different CTCF zinc fingers and observing the effects the deletions had on the ability of the protein to bind to different consensus sites [4,5,6,7,8]
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