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Cell-nonautonomously tunable actomyosin flows orient distinct cell division axes

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SummaryCell division axes during animal development are arranged in diverse orientations, but the molecular mechanisms underlying this diversity remain unclear. By focusing on oriented divisions that are independent of known microtubule/dynein pathways, we show here that the non-muscle myosin II motor is an extrinsically tunable force generator that orients cell division axes through cortical actomyosin flows. We identified three extracellular cues that generate different actomyosin flows. A single contact site locally inhibited myosin activity in a mechanosensitive manner to generate local flow asymmetry, while size asymmetry of two contact sites and Wnt signaling both polarized myosin activity and actomyosin flow, with the latter overriding mechanosensitive effects. These intracellular actomyosin flow anisotropies specify distinct division axes to establish the geometries of not onlyCaenorhabditis elegans4-, 6-, and 7-cell stage but also mouse 4-cell stage embryos. Tunable actomyosin flows together with microtubule/dynein pathways may specify diverse division axes across species.
Cold Spring Harbor Laboratory
Title: Cell-nonautonomously tunable actomyosin flows orient distinct cell division axes
Description:
SummaryCell division axes during animal development are arranged in diverse orientations, but the molecular mechanisms underlying this diversity remain unclear.
By focusing on oriented divisions that are independent of known microtubule/dynein pathways, we show here that the non-muscle myosin II motor is an extrinsically tunable force generator that orients cell division axes through cortical actomyosin flows.
We identified three extracellular cues that generate different actomyosin flows.
A single contact site locally inhibited myosin activity in a mechanosensitive manner to generate local flow asymmetry, while size asymmetry of two contact sites and Wnt signaling both polarized myosin activity and actomyosin flow, with the latter overriding mechanosensitive effects.
These intracellular actomyosin flow anisotropies specify distinct division axes to establish the geometries of not onlyCaenorhabditis elegans4-, 6-, and 7-cell stage but also mouse 4-cell stage embryos.
Tunable actomyosin flows together with microtubule/dynein pathways may specify diverse division axes across species.

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