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Stem Cell Reports ; 17(1): 53-67, 2022 01 11.
Article in English | MEDLINE | ID: mdl-34919813

ABSTRACT

Reprogramming of murine female somatic cells to induced pluripotent stem cells (iPSCs) is accompanied by X chromosome reactivation (XCR), by which the inactive X chromosome (Xi) in female somatic cells becomes reactivated. However, how Xi initiates reactivation during reprogramming remains poorly defined. Here, we used a Sendai virus-based reprogramming system to generate partially reprogrammed iPSCs that appear to be undergoing the initial phase of XCR. Allele-specific RNA-seq of these iPSCs revealed that XCR initiates at a subset of genes clustered near the centromere region. The initial phase of XCR occurs when the cells transit through mesenchymal-epithelial transition (MET) before complete shutoff of Xist expression. Moreover, regulatory regions of these genes display dynamic changes in lysine-demethylase 1a (KDM1A) occupancy. Our results identified clustered genes on the Xi that show reactivation in the initial phase of XCR during reprogramming and suggest a possible role for histone demethylation in this process.


Subject(s)
Cell Differentiation/genetics , Cellular Reprogramming/genetics , Multigene Family , Transcriptional Activation , X Chromosome Inactivation/genetics , Alleles , Animals , Biomarkers , Cellular Reprogramming Techniques , Fibroblasts , Gene Expression Profiling , High-Throughput Nucleotide Sequencing , Histone Demethylases , Mice , Real-Time Polymerase Chain Reaction , Single-Cell Analysis , Transcriptome
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