Role of Homeobox transcription factor encoding gene, Six in peripheral neural network
| Project/Area Number |
17590172
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
General anatomy (including Histology/Embryology)
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| Research Institution | Jichi Medical University |
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Principal Investigator |
YAMAKADO Makoto Jichi Medical University, Research associate, 医学部, 研究員 (80010114)
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| Co-Investigator(Kenkyū-buntansha) |
IKEDA Keiko Jichi Medical University, Associate Professor, 医学部, 准教授 (10265241)
KAWAKAMI Kiyoshi Jichi Medical University, Professor, 医学部, 教授 (10161283)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2006: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2005: ¥2,100,000 (Direct Cost: ¥2,100,000)
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| Keywords | Six1 / Six4 / Neurogenin / Sox10 / apoptosis / epibranchial ganglion / placode / neural crest / Neurogenin / Six / 遺伝子欠損マウス / 脳神経節 |
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| Research Abstract |
Six genes are homologues of the Drosophila sine oculis (so), which plays an essential role in the development of compound eye. There are six members of Six genes, from Six1 to Six6 in mice. Of these, Six1 and Six4 are expressed in sensory placodes, trigeminal ganglion, epibranchial ganglia, and neural crest cells during mouse development. To understand roles of Six genes in formation of sensory peripheral nervous system, we analyzed double homozygous knockout mice (Six1^<-/->Six4^<-/->). During the development of placode-derived and neural crest-derived cranial sensory ganglia, an early arrest of neurogenesis was observed in Six1^<-/->Six4^<-/->. The epibranchial progenitor cells failed to express Neurogenin1 and Neurogenin2, that are normally expressed and required for the determination of neuronal precursors in placodal-derived trigeminal and epibranchial ganglion, respectively at embryonic day (E) 9.5. NeuroD as well as Phox2b genes that are essential for neural differentiation and maintenance, were also dramatically decreased. Moreober, failure to activate normal differentiation program in placodal-derived neurons resulted in abnormal apoptosis of the progenitor cells in Six1^<-/->Six4^<-/->. We also observed that the delamination of placode epithelial cells to form ganglia were disturbed in Six1^<-/->Six4^<-/->. As for neural crest cell, the expression of Sox10 at E8.5 was not altered in wild-type and Six1^<-/->Six4^<-/->, while its expression at E10.5 was severely reduced in Six1^<-/->Six4^<-/->. These results indicated that production and migration of neural crest cells were not disturbed, but differentiation to glial cells were disrupted in Six1^<-/->Six4^<-/->.In sum, our data suggest that Six1 and Six4 play roles for early differentiation, delamination, and survival of the placodally derived cranial sensory neurons and differentiation of neural crest cells.
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(3 results)
Research Products
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