| Literature DB >> 29921581 |
Philipp G Maass1,2,3, Anja Weise4, Katharina Rittscher4, Julia Lichtenwald4, A Rasim Barutcu5, Thomas Liehr4, Atakan Aydin2,3, Yvette Wefeld-Neuenfeld3, Laura Pölsler6, Sigrid Tinschert6, John L Rinn5,7,8, Friedrich C Luft2,3,9, Sylvia Bähring2,3.
Abstract
Chromosomes occupy distinct interphase territories in the three-dimensional nucleus. However, how these chromosome territories are arranged relative to one another is poorly understood. Here, we investigated the inter-chromosomal interactions between chromosomes 2q, 12, and 17 in human mesenchymal stem cells (MSCs) and MSC-derived cell types by DNA-FISH We compared our findings in normal karyotypes with a three-generation family harboring a 2q37-deletion syndrome, featuring a heterozygous partial deletion of histone deacetylase 4 (HDAC4) on chr2q37. In normal karyotypes, we detected stable, recurring arrangements and interactions between the three chromosomal territories with a tissue-specific interaction bias at certain loci. These inter-chromosomal interactions were confirmed by Hi-C. Interestingly, the disease-related HDAC4 deletion resulted in displaced inter-chromosomal arrangements and altered interactions between the deletion-affected chromosome 2 and chromosome 12 and/or 17 in 2q37-deletion syndrome patients. Our findings provide evidence for a direct link between a structural chromosomal aberration and altered interphase architecture that results in a nuclear configuration, supporting a possible molecular pathogenesis.Entities:
Keywords: 2q37‐deletion syndrome; Mendelian disease; non‐homologous chromosomal contact; non‐random interphase architecture; nuclear repositioning
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Year: 2018 PMID: 29921581 PMCID: PMC6068439 DOI: 10.15252/embj.201696257
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598