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Epigenetic Regulation of the <i>H19</i> Chromatin Insulator in Development and Disease

<p>The coordinated regulation of gene expression must be tightly controlled for normal development to occur. In mammals, this issue is further complicated by the requirement of both the maternal and paternal genomes for normal development, reflecting the fact that a subset of genes are monoallelically expressed depending on parental inheritance, a phenomenon known as genomic imprinting. </p><p>The imprinted <i>H19</i> and <i>Igf2 </i>genes are often considered as paradigms of genomic imprinting, since their monoallelic expression patterns are coordinated <i>via</i> a short stretch of sequence upstream of <i>H19</i>, known as the imprinting control region (ICR). This region is differentially methylated, with specific CpG methylation on the paternal allele. It is shown here that the ICR harbours several maternal-specific hypersensitive sites, located in linker regions between positioned nucleosomes. Furthermore, this region functions as an orientation-dependent insulator, that binds the chromatin insulator factor CTCF. The hypothesis that the methylation status of the ICR dictates the activity of the <i>Igf2</i> gene 90 kb further upstream was confirmed by the demonstration that the insulator function is lost when the ICR is CpG methylated. </p><p>The ICR has previously been shown to act as a silencer when positioned in a promotor-proximal position. The cause of this silencing was shown to be distance-dependent, suggesting that the silencing features of the ICR depend on a chromatin conformation that renders adjacent sequences inaccessible to the RNA polymerase. These data issue a cautionary note with respect to the interpretation of silencer functions.</p><p>In several forms of cancer, the normally silent maternal <i>IGF2</i> gene is expressed, possibly as a result of loss of insulator function at the ICR. The utilisation of CTCF target-sites was analysed in different tumours, and was shown to be highly variable. Methylation analysis showed that potential loss of insulator function and gain of methylation at the maternal ICR did not always correlate with biallelic expression of <i>IGF2</i>. Further investigations uncovered a novel mechanism, in which the activation of the <i>IGF2</i> promoter was independent of insulator function in some cancers.</p><p>This thesis shows that the regulation of the imprinted state of <i>Igf2</i> depends on the formation of an epigenetically regulated chromatin insulator, and that the loss of <i>IGF2</i> imprinting in human cancer can be attributed to several mechanisms, including a novel mechanism that neutralises chromatin insulator function.</p>

Identiferoai:union.ndltd.org:UPSALLA/oai:DiVA.org:uu-3405
Date January 2003
CreatorsHolmgren, Claes
PublisherUppsala University, Department of Animal Development and Genetics, Uppsala : Acta Universitatis Upsaliensis
Source SetsDiVA Archive at Upsalla University
LanguageEnglish
Detected LanguageEnglish
TypeDoctoral thesis, comprehensive summary, text
RelationComprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, 1104-232X ; 825

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