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DNA Dynamics and Chromosome Structure

Parent-of-Origin-Specific Binding of Nuclear Hormone Receptor Complexes in the H19-Igf2 Imprinting Control Region

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Pages 4858-4868 | Received 12 Nov 2003, Accepted 27 Feb 2004, Published online: 27 Mar 2023
 

Abstract

Parent-of-origin-specific expression of the mouse insulin-like growth factor 2 gene (Igf2) and the closely linked H19 gene located on distal chromosome 7 is regulated by a 2.4-kb imprinting control region (ICR) located upstream of the H19 gene. In somatic cells, the maternally and paternally derived ICRs are hypo- and hypermethylated, respectively, with the former binding the insulator protein CCCTC-binding factor (CTCF) and acting to block access of enhancers to the Igf2 promoter. Here we report on a detailed in vivo footprinting analysis—using ligation-mediated PCR combined with in vivo dimethyl sulfate, DNase I, or UV treatment—of ICR sequences located outside of the CTCF binding domains. In mouse primary embryo fibroblasts carrying only maternal or paternal copies of distal chromosome 7, we have identified five prominent footprints specific to the maternal ICR. Each of the five footprinted areas contains at least two nuclear hormone receptor hexad binding sites arranged with irregular spacing. When combined with fibroblast nuclear extracts, these sequences interact with complexes containing retinoic X receptor alpha and estrogen receptor beta. More significantly, the footprint sequences bind nuclear hormone receptor complexes in male, but not female, germ cell extracts purified from fetuses at a developmental stage corresponding to the time of establishment of differential ICR methylation. These data are consistent with the possibility that nuclear hormone receptor complexes participate in the establishment of differential ICR methylation imprinting in the germ line.

We are grateful to Shih-Huey E. Tang for technical assistance, Lucy Brown, Claudio Spalla, and Jim Bolen for flow cytometry, Francisco Silva and Walter Tsark for blastocyst injection, Timothy O'Connor for his gift of AlkA protein, Steven Lloyd for endonuclease V, and Henry Sucov for the RXRα+/− mice. We also thank Frederic Chedin for his comments on the manuscript.

This work was supported by National Institutes of Health grant GM064378 to J.R.M. and National Cancer Institute grant CA33572-21 for the flow cytometry core facility.

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