ArticleCell reports2026
Nuclear speckle-associated perispeckle networks partition active chromatin into gene expression niches.
Article in Cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
12 authors.
Funding
Abstract
A subset of genes, reproducibly positioned adjacent to nuclear speckles (NS), amplify their expression only with NS contact. However, genome-wide gene expression differences inversely correlate with differences in NS distance. To resolve this paradox, we hypothesized the existence of additional "niches" away from, but spatially correlated with NS, that would enhance gene expression of adjacent genes. Analyzing NS-related proteins led us to identify two dynamic multi-protein perispeckle patterns extending outwards from NS. Highly active chromosome regions weakly associated with NS show close, NS-independent association with these perispeckle patterns. These perispeckle patterns persist after NS are eliminated. Whereas NS-associated genes are downregulated upon NS depletion, perispeckle-pattern associated genes are upregulated. Transcripts expressed from model intron-containing versus intronless genes associate differentially with these two patterns. We suggest that the interchromatin space is partitioned into additional gene expression "niches", surrounding and extending from NS, that may be involved in mRNA and gene dynamics.
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