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ZFIN ID: ZDB-PUB-160726-2
Microtubule-associated protein 9 (Map9/Asap) is required for the early steps of zebrafish development
Fontenille, L., Rouquier, S., Lutfalla, G., Giorgi, D.
Date: 2014
Source: Cell cycle (Georgetown, Tex.)   13(7): 1101-14 (Journal)
Registered Authors: Fontenille, Laura, Lutfalla, Georges
Keywords: microtubule-associated protein, microtubules, zebrafish, knockdown, mitosis, yolk syncytial layer, epiboly, gastrulation, development
MeSH Terms:
  • Animals
  • Apoptosis/genetics
  • Embryo, Nonmammalian/metabolism*
  • Microtubule-Associated Proteins/genetics
  • Microtubule-Associated Proteins/metabolism*
  • Mitosis/physiology
  • Signal Transduction
  • Spindle Apparatus/metabolism
  • Zebrafish/embryology
  • Zebrafish/metabolism*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed: 24553125 Full text @ Cell Cycle
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ABSTRACT
Microtubules are structural components of the cell cytoskeleton and key factors for mitosis and ciliogenesis in eukaryotes. The regulation of MT dynamics requires non-motor MAPs. We previously showed that, in human cells in culture, MAP9 (also named ASAP) is involved in MT dynamics and is essential for mitotic spindle formation and mitosis progression. Indeed, misexpression of MAP9 leads to severe mitotic defects and cell death. Here, we investigated the in vivo role of map9 during zebrafish development. Map9 is expressed mainly as a maternal gene. Within cells, Map9 is associated with the MT network of the mitotic spindle and with centrosomes. Morpholino-mediated depletion of map9 leads to early development arrest before completion of epiboly. Map9 localizes to the MT array of the YSL. This MT network is destroyed in Map9-depleted embryos, and injection of anti-map9 morpholinos directly in the nascent YSL leads to arrest of epiboly/gastrulation. Finally, map9 knockdown deregulates the expression of genes involved in endodermal differentiation, dorso–ventral and left–right patterning, and other MT-based functions. At low morpholino doses, the surviving embryos show dramatic developmental defects, spindle and mitotic defects, and increased apoptosis. Our findings suggest that map9 is a crucial factor in early zebrafish development by regulating different MT-based processes.
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