<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Klaasen SJ</submitter><funding>European Research Council</funding><pagination>604-609</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9300461</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>607(7919)</volume><pubmed_abstract>Chromosome segregation errors during cell divisions generate aneuploidies and micronuclei, which can undergo extensive chromosomal rearrangements such as chromothripsis&lt;sup>1-5&lt;/sup>. Selective pressures then shape distinct aneuploidy and rearrangement patterns-for example, in cancer&lt;sup>6,7&lt;/sup>-but it is unknown whether initial biases in segregation errors and micronucleation exist for particular chromosomes. Using single-cell DNA sequencing&lt;sup>8&lt;/sup> after an error-prone mitosis in untransformed, diploid cell lines and organoids, we show that chromosomes have different segregation error frequencies that result in non-random aneuploidy landscapes. Isolation and sequencing of single micronuclei from these cells showed that mis-segregating chromosomes frequently also preferentially beco</pubmed_abstract><journal>Nature</journal><pubmed_title>Nuclear chromosome locations dictate segregation error frequencies.</pubmed_title><pmcid>PMC9300461</pmcid><funding_grant_id>855158</funding_grant_id><pubmed_authors>de Vries SG</pubmed_authors><pubmed_authors>Vukusic K</pubmed_authors><pubmed_authors>Risteski P</pubmed_authors><pubmed_authors>Foijer F</pubmed_authors><pubmed_authors>Kind J</pubmed_authors><pubmed_authors>Klaasen SJ</pubmed_authors><pubmed_authors>Lens SMA</pubmed_authors><pubmed_authors>de Luca KL</pubmed_authors><pubmed_authors>Koprivec I</pubmed_authors><pubmed_authors>Tolic IM</pubmed_authors><pubmed_authors>Gerrits EM</pubmed_authors><pubmed_authors>Kops GJPL</pubmed_authors><pubmed_authors>Stimac V</pubmed_authors><pubmed_authors>Truong MA</pubmed_authors><pubmed_authors>van Jaarsveld RH</pubmed_authors><pubmed_authors>Marques JF</pubmed_authors><pubmed_authors>Bakker B</pubmed_authors><pubmed_authors>Kodba S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nuclear chromosome locations dictate segregation error frequencies.</name><description>Chromosome segregation errors during cell divisions generate aneuploidies and micronuclei, which can undergo extensive chromosomal rearrangements such as chromothripsis&lt;sup>1-5&lt;/sup>. Selective pressures then shape distinct aneuploidy and rearrangement patterns-for example, in cancer&lt;sup>6,7&lt;/sup>-but it is unknown whether initial biases in segregation errors and micronucleation exist for particular chromosomes. Using single-cell DNA sequencing&lt;sup>8&lt;/sup> after an error-prone mitosis in untransformed, diploid cell lines and organoids, we show that chromosomes have different segregation error frequencies that result in non-random aneuploidy landscapes. Isolation and sequencing of single micronuclei from these cells showed that mis-segregating chromosomes frequently also preferentially beco</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-05T15:05:16.894Z</modification><creation>2025-02-19T03:52:57.052Z</creation></dates><accession>S-EPMC9300461</accession><cross_references><pubmed>35831506</pubmed><doi>10.1038/s41586-022-04938-0</doi></cross_references></HashMap>