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Wise, N.

Publications and source records attributed to Wise, N..

2 recordsLinked to original sources

Formation of an RNA-mediated nuclear compartment

Mammalian nuclei are spatially compartmentalized so that active and inactive segments of the genome occupy separate sub-nuclear neighborhoods. Compartments are often found in association with nuclear structures such as the nuclear lamina, nucleoli, and nuclear speckles (speckles), suggesting links between them. The molecular mechanisms by which compartments form remain largely unknown. Speckles are nuclear bodies that contain high concentrations of RNA splicing factors and associated chromatin has a high density of highly expressed genes. Combining liquid chromatin Hi-C to quantify chromatin interaction lifetimes genome-wide, immunofluorescence, fluorescence in situ hybridization, live cell imaging, and nascent transcript analysis, we have determined the biophysical and molecular basis of the speckle-associated chromosomal compartment. We find that genomic regions making up this compartment are stably glued together. Surprisingly, removal of speckles by rapid depletion of SON and SRRM2 that form the structural scaffold of these bodies shows that this stable association is not dependent on the speckle itself. Instead, we find that RNA molecules are the molecular glue that forms the biophysical basis of the speckle chromatin compartment. Based on observations that promoters and enhancers are also engaged in stable long-lived chromatin interactions that are independent of RNA, we propose a pathway for formation of the speckle chromosomal compartment: Initial stable clustering of promoters and enhancers is followed by production of (nascent) RNA. The exceptionally high density of GC-rich RNA emerging from speckle-associated loci forms a glue that holds these loci together and facilitates recruitment of speckle components. The result is a structurally stable nuclear compartment that facilitates efficient splicing.

genomics↗

CRISPR-FOIL: A Programmable CRISPR Tool to Engineer and Illuminate Chromatin Folding in Live Human Cells

Chromatin organization plays a critical role in regulating gene expression. Chromatin compaction represses gene expression by physically restricting the access of the transcriptional machinery to DNA, while spatial proximity between enhancers and promoters, often mediated by chromatin loops, is essential for gene activation. To investigate the regulatory mechanisms underlying loop formation and chromatin compaction, as well as their effects on gene expression, we developed CRISPR-FOIL (utilizing CRISPR to FOld and ILluminate chromosomal DNA), a novel programmable platform for engineering chromatin loops and inducing chromatin compaction in live cells. CRISPR-FOIL anchors pairs of genomic loci in proximity by engineered single-guide RNAs (sgRNAs), resulting in an artificial chromatin loop. The fused two CRISPR-Sirius gRNAs enable genomic loci to be visualized through fluorescent RNA coat proteins in various colors. In addition, multiple CRISPR-FOIL complexes can act cooperatively to drive chromatin compaction. These results establish CRISPR-FOIL as a powerful tool for engineering chromatin organization in live cells and highlight its potential as a therapeutic platform for gene regulation and disease control.

cell biology↗