A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors.
Ontology highlight
ABSTRACT: Transcriptional networks governing cardiac precursor cell (CPC) specification are incompletely understood owing, in part, to limitations in distinguishing CPCs from non-cardiac mesoderm in early gastrulation. We leveraged detection of early cardiac lineage transgenes within a granular single-cell transcriptomic time course of mouse embryos to identify emerging CPCs and describe their transcriptional profiles. Mesp1, a transiently expressed mesodermal transcription factor, is canonically described as an early regulator of cardiac specification. However, we observed perdurance of CPC transgene-expressing cells in Mesp1 mutants, albeit mislocalized, prompting us to investigate the scope of the role of Mesp1 in CPC emergence and differentiation. Mesp1 mutant CPCs failed to robustly activate ma
SUBMITTER: Krup AL
PROVIDER: S-EPMC10259516 | biostudies-literature | 2023 May
REPOSITORIES: biostudies-literature
ACCESS DATA