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The MIG-15 NIK kinase acts cell-autonomously in neuroblast polarization and migration in C. elegans.
- Source :
-
Developmental biology [Dev Biol] 2008 Dec 15; Vol. 324 (2), pp. 245-57. Date of Electronic Publication: 2008 Sep 24. - Publication Year :
- 2008
-
Abstract
- Cell migration is a fundamental process in animal development, including development of the nervous system. In C. elegans, the bilateral QR and QL neuroblasts undergo initial anterior and posterior polarizations and migrations before they divide to produce neurons. A subsequent Wnt signal from the posterior instructs QL descendants to continue their posterior migration. Nck-interacting kinases (NIK kinases) have been implicated in cell and nuclear migration as well as lamellipodia formation. Studies here show that the C. elegans MIG-15 NIK kinase controls multiple aspects of initial Q cell polarization, including the ability of the cells to polarize, to maintain polarity, and to migrate. These data suggest that MIG-15 acts independently of the Wnt signal that controls QL descendant posterior migration. Furthermore, MIG-15 affects the later migrations of neurons generated from Q cell division. Finally, a mosaic analysis indicates that MIG-15 acts cell-autonomously in Q descendant migration.
- Subjects :
- Animals
Animals, Genetically Modified embryology
Animals, Genetically Modified genetics
Animals, Genetically Modified metabolism
Caenorhabditis elegans genetics
Caenorhabditis elegans metabolism
Caenorhabditis elegans Proteins genetics
Neurons metabolism
Protein Serine-Threonine Kinases genetics
Wnt Proteins genetics
Wnt Proteins metabolism
Caenorhabditis elegans embryology
Caenorhabditis elegans Proteins metabolism
Cell Movement
Cell Polarity
Neurons cytology
Protein Serine-Threonine Kinases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1095-564X
- Volume :
- 324
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Developmental biology
- Publication Type :
- Academic Journal
- Accession number :
- 18840424
- Full Text :
- https://doi.org/10.1016/j.ydbio.2008.09.014