Ablation of the 14-3-3gamma Protein Results in Neuronal Migration Delay and Morphological Defects in the Developing Cerebral Cortex

scientific article published on 22 August 2015

Ablation of the 14-3-3gamma Protein Results in Neuronal Migration Delay and Morphological Defects in the Developing Cerebral Cortex is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/DNEU.22335
P8608Fatcat IDrelease_5ahxd2qernhn3ctsyx2thc2pbi
P698PubMed publication ID26297819

P50authorKazuhito Toyo-okaQ79793170
P2093author name stringPeter W Baas
Brett Cornell
Courtney Marshall
Tomoka Wachi
Vladimir Zhukarev
P2860cites workElectroporation and RNA interference in the rodent retina in vivo and in vitroQ35120935
Neurogenin2 regulates the initial axon guidance of cortical pyramidal neurons projecting medially to the corpus callosumQ35215714
14-3-3 proteins: a highly conserved, widespread family of eukaryotic proteinsQ35624026
14-3-3 Proteins--a focus on cancer and human diseaseQ35879488
Role of 14-3-3 proteins in eukaryotic signaling and developmentQ36241760
Reelin controls neuronal positioning by promoting cell-matrix adhesion via inside-out activation of integrin α5β1Q36342370
14-3-3 proteins: a historic overviewQ36470005
Genetic mechanisms underlying abnormal neuronal migration in classical lissencephalyQ36998695
Selective 14-3-3γ induction quenches p-β-catenin Ser37/Bax-enhanced cell death in cerebral cortical neurons during ischemiaQ37726133
Miller-Dieker syndrome: lissencephaly and monosomy 17p.Q40269627
Monomeric 14-3-3ζ has a chaperone-like activity and is stabilized by phosphorylated HspB6.Q41824229
Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephalyQ41934375
14-3-3-affinity purification of over 200 human phosphoproteins reveals new links to regulation of cellular metabolism, proliferation and traffickingQ42125847
Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division.Q43072719
Cytoarchitectonic anomalies in a genetically based disorder: Williams syndrome.Q48155254
Case report: Neuronal migration disorder associated with chromosome 15q13.3 duplication in a boy with autism and seizures.Q48842137
Efficient in utero gene transfer system to the developing mouse brain using electroporation: visualization of neuronal migration in the developing cortexQ48919857
Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiencyQ50345055
Isolated lissencephaly: report of four patients from two unrelated families.Q52060137
Expression of 14-3-3γ in patients with breast cancer: correlation with clinicopathological features and prognosisQ84278665
Involvement of 14-3-3γ overexpression in extrahepatic metastasis of hepatocellular carcinomaQ85092497
14-3-3γ-Mediated transport of plakoglobin to the cell border is required for the initiation of desmosome assembly in vitro and in vivoQ87417157
Regulation of RAF activity by 14-3-3 proteins: RAF kinases associate functionally with both homo- and heterodimeric forms of 14-3-3 proteinsQ24320264
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22Q24517924
Neuronal migration abnormalities and its possible implications for schizophreniaQ26824953
Beta2 integrin phosphorylation on Thr758 acts as a molecular switch to regulate 14-3-3 and filamin bindingQ27650823
Characterization of 14-3-3-ζ Interactions with Integrin TailsQ27678611
The kinesin-like motor protein KIF1C occurs in intact cells as a dimer and associates with proteins of the 14-3-3 familyQ28137828
14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndromeQ28178021
Identification of a novel interaction between integrin beta1 and 14-3-3betaQ28213843
The serine-rich domain from Crk-associated substrate (p130cas) is a four-helix bundleQ28242010
A c-Cbl yeast two hybrid screen reveals interactions with 14-3-3 isoforms and cytoskeletal componentsQ28254545
Directional persistence of migrating cells requires Kif1C-mediated stabilization of trailing adhesionsQ28281353
Lissencephaly and other malformations of cortical development: 1995 updateQ28284003
The structural basis for 14-3-3:phosphopeptide binding specificityQ29547190
Methods for cell and particle trackingQ29617370
PI 3-kinase-dependent phosphorylation of Plk1-Ser99 promotes association with 14-3-3γ and is required for metaphase-anaphase transitionQ30540402
Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype.Q30543830
Genetic basis of developmental malformations of the cerebral cortexQ30932048
Neuronal migration disorders, genetics, and epileptogenesisQ30990797
14-3-3gamma induces oncogenic transformation by stimulating MAP kinase and PI3K signalingQ33632327
Unchanged survival rates of 14-3-3gamma knockout mice after inoculation with pathological prion proteinQ33822953
The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changesQ33847352
Off-target effect of doublecortin family shRNA on neuronal migration associated with endogenous microRNA dysregulationQ33861313
Depletion of 14-3-3γ reduces the surface expression of Transient Receptor Potential Melastatin 4b (TRPM4b) channels and attenuates TRPM4b-mediated glutamate-induced neuronal cell death.Q33970029
Human brain malformations and their lessons for neuronal migrationQ34088067
How do 14-3-3 proteins work?-- Gatekeeper phosphorylation and the molecular anvil hypothesisQ34120299
14-3-3ε and ζ regulate neurogenesis and differentiation of neuronal progenitor cells in the developing brain.Q34123851
Cell migration and cerebral cortical developmentQ34216765
14-3-3 proteins: active cofactors in cellular regulation by serine/threonine phosphorylationQ34439988
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humansQ34600929
P433issue6
P1104number of pages15
P304page(s)600-614
P577publication date2015-08-22
P1433published inDevelopmental NeurobiologyQ15716734
P1476titleAblation of the 14-3-3gamma Protein Results in Neuronal Migration Delay and Morphological Defects in the Developing Cerebral Cortex
P478volume76

Reverse relations

cites work (P2860)
Q4269467714-3-3 Proteins in Brain Development: Neurogenesis, Neuronal Migration and Neuromorphogenesis
Q6423843714-3-3γ Haploinsufficient Mice Display Hyperactive and Stress-sensitive Behaviors
Q47372760Complete ablation of the 14-3-3epsilon protein results in multiple defects in neuropsychiatric behaviors.
Q38640554De Novo Mutations in YWHAG Cause Early-Onset Epilepsy
Q41672511GFAP expression in injured astrocytes in rats
Q90454161Importin-8 Modulates Division of Apical Progenitors, Dendritogenesis and Tangential Migration During Development of Mouse Cortex
Q50309807Regulation of neuronal morphogenesis by 14-3-3epsilon (Ywhae) via the microtubule binding protein, doublecortin