4.7 Article

Furry is required for cell movements during gastrulation and functionally interacts with NDR1

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41598-021-86153-x

Keywords

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Funding

  1. Agencia Nacional de Promocion Cientifica y Tecnologica of Argentina [PICT-2013-0381]
  2. Fondo para la Investigacion Cientifica y Tecnologica [2013-1301, 2014-3658]
  3. Max-Planck-Gesellschaft (Partner Group)
  4. Secretaria de Ciencia y Tecnica [20020170100755BA]
  5. CONICET Doctoral Fellowship Program
  6. National Institutes of Health (NICHD) [R01 HD044750]
  7. National Institutes of Health (NHLBI) [R01 R01 HL136566]

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The Fry gene plays a crucial role in morphogenetic processes during gastrulation in Xenopus, impacting cell movement and morphological polarization. Additionally, Fry is involved in the regulation of dorsal mesoderm gene expression during vertebrate development. Functional interaction between Fry and NDR1 kinase suggests an evolutionarily conserved complex required for morphogenesis.
Gastrulation is a key event in animal embryogenesis during which germ layer precursors are rearranged and the embryonic axes are established. Cell polarization is essential during gastrulation, driving asymmetric cell division, cell movements, and cell shape changes. The furry (fry) gene encodes an evolutionarily conserved protein with a wide variety of cellular functions, including cell polarization and morphogenesis in invertebrates. However, little is known about its function in vertebrate development. Here, we show that in Xenopus, Fry plays a role in morphogenetic processes during gastrulation, in addition to its previously described function in the regulation of dorsal mesoderm gene expression. Using morpholino knock-down, we demonstrate a distinct role for Fry in blastopore closure and dorsal axis elongation. Loss of Fry function drastically affects the movement and morphological polarization of cells during gastrulation and disrupts dorsal mesoderm convergent extension, responsible for head-to-tail elongation. Finally, we evaluate a functional interaction between Fry and NDR1 kinase, providing evidence of an evolutionarily conserved complex required for morphogenesis.

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