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Functional analysis of homeobox genes in neuromere development : Mouse molecular genetical approch

Functional analysis of homeobox genes in neuromere development : Mouse molecular genetical approch
神经节发育中同源盒基因的功能分析:小鼠分子遗传学方法
批准号:
09680750
负责人:
HANAOKA Kazunori
金额:
$1.86万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1998

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中文摘要
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英文摘要
(1) Somites are the source of hypaxial musculature including skeletal muscles of the limb, tongue and the trunk. To get insight into the function of mouse Lbxl homeobox gene in the early somitic mesoderni differentiation, in situhybridization analyses was performed. At 4-6 somite stage (8dpc), Lbxl was first expressed in the lateral portion of the epithelial somite and of dermomyotomal epithelium. This was contrast to the expression of myf-5 in the medial region of the somite. Then the lateral expression of Lbxl in somitic mesoderm occurred regionally along the anterior-posterior body axis. Later at 10 dpc (stage 1 for limb bud development) Lbxl-positive migrating cells originated from the lateral dermomyotomal lips at occipital, forelimb and hindlinib levels. They also expressed Pax-3 and c-met known as markers of the migrating limb muscle precursor cells. In stage 4 hindlimb bud (11.5 dpc), the dorsal and ventral muscle precursor populations expressed Lbxl. In stage 8 forelimb buds ( … More 12.5 dpc), Lbxl expression was reduced in the proximal muscle masses where the highly expression of myogenin accompanying the muscle differentiation was detected. These results suggest that mouse Lbxl might be involved in the commitment or determination of a muscle cell subpopulation during the hypaxial musculature development.(2) cHox11L2, the chick counterpart of mouse Hox11L2, was isolated. cHox11L2 was expressed in the developing chick peripheral nervous system, i. e. sensory cranial nerves of the placodal ectoderm origin, sympathetic ganglia, dorsal root ganglia and enteric ganglia as well as the limited population of the spinal cord. In neuronal derivatives of the neural crest, dHox11L2 was expressed in the postmigratory cells and not in the migrating neural crest cells. Furthermore, Intense signals of cHox11L2 mRNA were detected even in the spinal cord and the dorsal root of 10 day embryo. These results suggest that cHox11L2 might play a role in the determination and/or maintenance of neuronal differentiation during chick nervous system development. Less
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K.Uchiyama, R.Ohtuka and Hanaoka K.: "cHox11L2, a Hox11 related gene, is expressed in the peripheral nervous system and subpopulation of spinal cord during chick development" Neurosci. Lett. In press.
K.Uchiyama、R.Ohtuka 和 Hanaoka K.:“cHox11L2 是一种 Hox11 相关基因,在雏鸡发育过程中在周围神经系统和脊髓亚群中表达” Neurosci。
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Kameya S., Miyagoe Y., Nonaka I., Ikemoto T., Endo M., Hanaoka K., Nabeshima Y., and Takeda S.: "alphal-syntrophin gene disruptionresults in the absence of neuronal-type nitric oxide synthetase at the salcolemma, but does not induce muscle degeneration" J
Kameya S.、Miyagoe Y.、Nonaka I.、Ikemoto T.、Endo M.、Hanaoka K.、Nabeshima Y. 和 Takeda S.:“α-肌营养蛋白基因破坏导致神经元型一氧化氮合成酶缺失
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K.Tomizuka et al.: "Functional expression and germlinetransmission of human chromosome fragment in chimeric mice" Nature Genet. 16. 133-143 (1977)
K.Tomizuka 等人:“嵌合小鼠中人类染色体片段的功能表达和种系传递”Nature Genet。
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Miyagoe Y et al.: "Laminin α 2 chain null mutant mice bytargeted disrupnon of the Lama 2 gene:A new model of merosin-deficient congenital muscular dystrophy" FEBS Letters. 415. 33-39 (1977)
Miyagoe Y 等人:“Laminin α 2 链无效突变小鼠通过 Lama 2 基因的靶向破坏:一种新的 merosin 缺陷型先天性肌营养不良模型”FEBS Letters 415. 33-39 (1977)。
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9
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      20500367
    • 项目类别:
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    • 项目类别:
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    • 资助金额:
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    Introduction of human mini-chromosome vector carrying human dystrophin gene into the mdx mice
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    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
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    • 财政年份:
      2002
    • 负责人:
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