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The periphery of nuclear speckles defines a spatially and temporally regulated compartment of long-lived intron-retained RNAs that resolves during mitosis
Abstract RNA localization adds a fundamental layer to gene expression by determining when and where translation-ready mRNAs become available, yet how this timing is coordinated with nuclear architecture and cell-cycle progression remains unclear. Here we identify a subnuclear RNA niche at the nuclear speckle periphery that couples intron retention to cell-cycle-timed RNA release.
Inter-chromosomal contacts demarcate genome topology along a spatial gradient - Nature Communications
Abstract Non-homologous chromosomal contacts (NHCCs) between different chromosomes participate considerably in gene and genome regulation. Due to analytical challenges, NHCCs are currently considered as singular, stochastic events, and their extent and fundamental principles across cell types remain controversial. We develop a supervised and unsupervised learning algorithm, termed Signature, to call NHCCs in Hi-C datasets to advance our understanding of genome topology.
Systematic mapping of nuclear domain-associated transcripts reveals speckles and lamina as hubs of functionally distinct retained introns
Ahn E.Y. DeKelver R.C. Lo M.C. Nguyen T.A. Matsuura S. Boyapati A. Pandit S. Fu X.D. Zhang D.E. SON controls cell-cycle progression by coordinated regulation of RNA splicing. Mol. Cell. 2011; 42: 185-198 Amit M. Donyo M. Hollander D. Goren A. Kim E. Gelfman S. Lev-Maor G. Burstein D. Schwartz S. Postolsky B. et al. Differential GC content between exons and introns establishes distinct strategies of splice-site recognition. Cell Rep.
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