N1-Src Kinase Is Required for Primary Neurogenesis in Xenopus tropicalis

The presence of the neuronal-specific N1-Src splice variant of the C-Src tyrosine kinase is conserved through vertebrate evolution, suggesting an important role in complex nervous systems. Alternative splicing involving an -specific microexon leads to a 5 or 6 aa insertion into the SH3 domain of Src...

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Published in:	The Journal of neuroscience Vol. 37; no. 35; pp. 8477 - 8485
Main Authors:	Lewis, Philip A, Bradley, Isobel C, Pizzey, Alastair R, Isaacs, Harry V, Evans, Gareth J O
Format:	Journal Article
Language:	English
Published:	United States Society for Neuroscience 30-08-2017
Subjects:	Alternative splicing Animals Antisense RNA Brain Cell adhesion Cell adhesion & migration Cell Differentiation - physiology Cell migration Cytoskeleton Differentiation Embryogenesis Embryonic growth stage Embryos Enzyme Activation Evolution Frogs Growth cones Hybridization analysis Kinases Male Nervous system Neural plate Neural Stem Cells - cytology Neural Stem Cells - enzymology Neurogenesis Neurogenesis - physiology Neurons Neurons - cytology Neurons - enzymology Neurotransmission Nucleic acids Protein Isoforms Protein-tyrosine kinase Src protein src-Family Kinases - genetics src-Family Kinases - metabolism Tyrosine Vertebrates Xenopus Xenopus - anatomy & histology Xenopus - physiology Xenopus neurogenesis embryo splicing morpholino tyrosine kinase
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Summary:	The presence of the neuronal-specific N1-Src splice variant of the C-Src tyrosine kinase is conserved through vertebrate evolution, suggesting an important role in complex nervous systems. Alternative splicing involving an -specific microexon leads to a 5 or 6 aa insertion into the SH3 domain of Src. A prevailing model suggests that N1-Src regulates neuronal differentiation via cytoskeletal dynamics in the growth cone. Here we investigated the role of n1-src in the early development of the amphibian , and found that expression is regulated in embryogenesis, with highest levels detected during the phases of primary and secondary neurogenesis. hybridization analysis, using locked nucleic acid oligo probes complementary to the microexon, indicates that expression is highly enriched in the open neural plate during neurula stages and in the neural tissue of adult frogs. Given the expression pattern, we investigated a possible role for n1-src in neurogenesis. Using splice site-specific antisense morpholino oligos, we inhibited splicing, while preserving expression. Differentiation of neurons in the primary nervous system is reduced in -knockdown embryos, accompanied by a severely impaired touch response in later development. These data reveal an essential role for n1-src in amphibian neural development and suggest that alternative splicing of C-Src in the developing vertebrate nervous system evolved to regulate neurogenesis. The Src family of nonreceptor tyrosine kinases acts in signaling pathways that regulate cell migration, cell adhesion, and proliferation. Srcs are also enriched in the brain, where they play key roles in neuronal development and neurotransmission. Vertebrates have evolved a neuron-specific splice variant of C-Src, N1-Src, which differs from C-Src by just 5 or 6 aa. N1-Src is poorly understood and its high similarity to C-Src has made it difficult to delineate its function. Using antisense knockdown of the microexon, we have studied neuronal development in the embryo in the absence of , while preserving Loss of n1-src causes a striking absence of primary neurogenesis, implicating n1-src in the specification of neurons early in neural development.
Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: P.A.L., H.V.I., and G.J.O.E. designed research; P.A.L., I.C.B., and A.R.P. performed research; P.A.L., I.C.B., A.R.P., H.V.I., and G.J.O.E. analyzed data; P.A.L., I.C.B., H.V.I., and G.J.O.E. wrote the paper. H.V.I. and G.J.O.E. contributed equally to this work. P.A.L. and I.C.B. contributed equally to this work.
ISSN:	0270-6474 1529-2401
DOI:	10.1523/JNEUROSCI.3881-16.2017