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Par3-mInsc and G?i3 cooperate to promote oriented epidermal cell divisions through LGN.


ABSTRACT: Asymmetric cell divisions allow stem cells to balance proliferation and differentiation. During embryogenesis, murine epidermis expands rapidly from a single layer of unspecified basal layer progenitors to a stratified, differentiated epithelium. Morphogenesis involves perpendicular (asymmetric) divisions and the spindle orientation protein LGN, but little is known about how the apical localization of LGN is regulated. Here, we combine conventional genetics and lentiviral-mediated in vivo RNAi to explore the functions of the LGN-interacting proteins Par3, mInsc and G?i3. Whereas loss of each gene alone leads to randomized division angles, combined loss of Gnai3 and mInsc causes a phenotype of mostly planar divisions, akin to loss of LGN. These findings lend experimental support for the hitherto untested model that Par3-mInsc and G?i3 act cooperatively to polarize LGN and promote perpendicular divisions. Finally, we uncover a developmental switch between delamination-driven early stratification and spindle-orientation-dependent differentiation that occurs around E15, revealing a two-step mechanism underlying epidermal maturation.

SUBMITTER: Williams SE 

PROVIDER: S-EPMC4159251 | biostudies-literature | 2014 Aug

REPOSITORIES: biostudies-literature

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Par3-mInsc and Gαi3 cooperate to promote oriented epidermal cell divisions through LGN.

Williams Scott E SE   Ratliff Lyndsay A LA   Postiglione Maria Pia MP   Knoblich Juergen A JA   Fuchs Elaine E  

Nature cell biology 20140713 8


Asymmetric cell divisions allow stem cells to balance proliferation and differentiation. During embryogenesis, murine epidermis expands rapidly from a single layer of unspecified basal layer progenitors to a stratified, differentiated epithelium. Morphogenesis involves perpendicular (asymmetric) divisions and the spindle orientation protein LGN, but little is known about how the apical localization of LGN is regulated. Here, we combine conventional genetics and lentiviral-mediated in vivo RNAi t  ...[more]

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