ArticleMethods in molecular biology (Clifton, N.J.)2026
Investigating Dysregulated X Chromosome Inactivation in Human B Cells and Plasmacytoid Dendritic Cells by RNA FISH.
Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
RNA fluorescent in situ hybridization (RNA FISH) has been widely used to monitor the allelic expression of primary transcripts and/or non-coding RNAs in individual cell nuclei. In particular, this method is a gold standard to establish which X-linked genes undergo or escape X chromosome inactivation in female mammalian cells by combining probes specific of the X-linked transcripts of interest with probe specific of the long-non-coding XIST RNA that coats the inactive X (Xi) territory. Here we describe the dual RNA FISH protocol we have developed to track (1) the coating of the Xi by the XIST RNA and (2) the expression of the X-linked TLR7 gene on the active and inactive X chromosomes, in human plasmacytoid dendritic cells (pDCs) and in female B lymphocytes induced to differentiate into plasmablasts or pre-Antibody Secreting Cells (pre-ASC) upon activation of either TLR7 or TLR9.
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