Buendia, Gustavo A. RuizLeleu, MarionMarzetta, FlaviaVanzan, LudovicaTan, Jennifer Y.Ythier, VictorRandall, Emma L.Marques, Ana C.Baubec, TuncayMurr, RabihXenarios, IoannisDion, Vincent2020-07-302020-07-302020-07-302020-07-0110.1126/sciadv.aaz4012https://infoscience.epfl.ch/handle/20.500.14299/170468WOS:000548735500009Expanded CAG/CTG repeats underlie 13 neurological disorders, including myotonic dystrophy type 1 (DM1) and Huntington's disease (HD). Upon expansion, disease loci acquire heterochromatic characteristics, which may provoke changes to chromatin conformation and thereby affect both gene expression and repeat instability. Here, we tested this hypothesis by performing 4C sequencing at the DMPK and HTT loci from DM1 and HD-derived cells. We find that allele sizes ranging from 15 to 1700 repeats displayed similar chromatin interaction profiles. This was true for both loci and for alleles with different DNA methylation levels and CTCF binding. Moreover, the ectopic insertion of an expanded CAG repeat tract did not change the conformation of the surrounding chromatin. We conclude that CAG/CTG repeat expansions are not enough to alter chromatin conformation in cis. Therefore, it is unlikely that changes in chromatin interactions drive repeat instability or changes in gene expression in these disorders.Multidisciplinary SciencesScience & Technology - Other Topicshistone modificationsfriedreichs-ataxiaepigenetic changesread alignmentcgg repeatgeneinstabilityfmr1methylationbindingtext::journal::journal article::research article