| Literature DB >> 28826820 |
Frederic Koch1, Manuela Scholze1, Lars Wittler1, Dennis Schifferl1, Smita Sudheer1, Phillip Grote1, Bernd Timmermann2, Karol Macura1, Bernhard G Herrmann3.
Abstract
The spinal cord and mesodermal tissues of the trunk such as the vertebral column and skeletal musculature derive from neuro-mesodermal progenitors (NMPs). Sox2, Brachyury (T), and Tbx6 have been correlated with NMP potency and lineage choice; however, their exact role and interaction in these processes have not yet been revealed. Here we present a global analysis of NMPs and their descending lineages performed on purified cells from embryonic day 8.5 wild-type and mutant embryos. We show that T, cooperatively with WNT signaling, controls the progenitor state and the switch toward the mesodermal fate. Sox2 acts antagonistically and promotes neural development. T is also involved in remodeling the chromatin for mesodermal development. Tbx6 reinforces the mesodermal fate choice, represses the progenitor state, and confers paraxial fate commitment. Our findings refine previous models and establish molecular principles underlying mammalian trunk development, comprising NMP maintenance, lineage choice, and mesoderm formation.Entities:
Keywords: NMP; chromatin; lineage choice; mesoderm; mouse; neuro-mesodermal progenitors; neuroectoderm; single-cell analysis; transcriptome; trunk development
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Year: 2017 PMID: 28826820 DOI: 10.1016/j.devcel.2017.07.021
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270