| Literature DB >> 32574593 |
Jean-François Poulin1, Milagros Pereira Luppi2, Caitlyn Hofer2, Giuliana Caronia2, Pei-Ken Hsu2, C Savio Chan3, Rajeshwar Awatramani4.
Abstract
Lineage tracing aims to identify the progeny of a defined population of dividing progenitor cells, a daunting task in the developing central nervous system where thousands of cell types are generated. In mice, lineage analysis has been accomplished using Cre recombinase to indelibly label a defined progenitor population and its progeny. However, the interpretation of historical recombination events is hampered by the fact that driver genes are often expressed in both progenitors and postmitotic cells. Genetically inducible approaches provide temporal specificity but are afflicted by mosaicism and toxicity. Here, we present PRISM, a progenitor-restricted intersectional fate mapping approach in which Flp recombinase expression is both dependent on Cre and restricted to neural progenitors, thus circumventing the aforementioned confounds. This tool can be used in conjunction with existing Cre lines making it broadly applicable. We applied PRISM to resolve two developmentally important, but contentious, lineages-Shh and Cux2.Entities:
Keywords: Cux2; Sonic hedgehog; development; fate mapping; forebrain; intersectional genetics; lineage; neuron; progenitor; recombinase
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Year: 2020 PMID: 32574593 PMCID: PMC7778471 DOI: 10.1016/j.devcel.2020.05.019
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270