Defining human cardiac transcription factor hierarchies using integrated single-cell heterogeneity analysis.
Ontology highlight
ABSTRACT: Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have become a powerful tool for human disease modeling and therapeutic testing. However, their use remains limited by their immaturity and heterogeneity. To characterize the source of this heterogeneity, we applied complementary single-cell RNA-seq and bulk RNA-seq technologies over time during hiPSC cardiac differentiation and in the adult heart. Using integrated transcriptomic and splicing analysis, more than half a dozen distinct single-cell populations were observed, several of which were coincident at a single time-point, day 30 of differentiation. To dissect the role of distinct cardiac transcriptional regulators associated with each cell population, we systematically tested the effect of a gain or loss of three t
SUBMITTER: Churko JM
PROVIDER: S-EPMC6249224 | biostudies-literature | 2018 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA