Abstract
AbstractGenome differential positioning within interphase nuclei remains poorly explored. We extended and validated TSA-seq to map genomic regions near nucleoli and pericentric heterochromatin in four human cell lines. Our study confirmed that smaller chromosomes localize closer to nucleoli but further deconvolved this by revealing a preference for chromosome arms below 36-46 Mbp in length. We identified two lamina associated domain subsets through their differential nuclear lamina versus nucleolar positioning in different cell lines which showed distinctive patterns of DNA replication timing and gene expression across all cell lines. Unexpectedly, active, nuclear speckle-associated genomic regions were found near typically repressive nuclear compartments, which is attributable to the close proximity of nuclear speckles and nucleoli in some cell types, and association of centromeres with nuclear speckles in hESCs. Our study points to a more complex and variable nuclear genome organization than suggested by current models, as revealed by our TSA-seq methodology.
Publisher
Cold Spring Harbor Laboratory
Reference56 articles.
1. Heterochromatin
2. Das Heterochromatin der Moose;I. Jahrb Wiss Bot,1928
3. Emil Heitz and the concept of heterochromatin: longitudinal chromosome differentiation was recognized fifty years ago;Am J Hum Genet,1979
4. The nuclear lamina and heterochromatin: a complex relationship
5. Lamina-Associated Domains: Links with Chromosome Architecture, Heterochromatin, and Gene Repression