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Analysis of brain development in TGIF deficient mouse

Analysis of brain development in TGIF deficient mouse
TGIF缺陷小鼠大脑发育分析
批准号:
6906888
负责人:
YAN CHEN
金额:
$7.58万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-04-01 至 2007-03-31

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中文摘要
翻译
描述(由申请人提供):这是一项R 03申请,重点关注TGIF基因敲除小鼠的初始表征,以及使用该小鼠模型探索TGIF与脑发育缺陷的潜在联系,尤其是与前脑无裂畸形(HPE)疾病相关的联系。HPE是一种人类遗传性疾病,具有脑和颅面发育的特征性缺陷。HPE是人类前脑发育中最常见的结构缺陷,在大脑发育早期控制神经管模式的基因中发现了突变。TG-相互作用因子(TG-interacting factor,TGIF)是一种同源异型盒蛋白,通过与Smad蛋白直接结合,作为转录辅阻遏物调节转化生长因子β(TGF-β)诱导的基因转录。在HPE患者中发现了TGIF的突变,表明TGIF可能在前脑发育中起重要作用。目前,TGIF的体内功能尚不清楚。 本研究拟采用以下两种策略来阐明TGIF在脑发育中的生物学功能:(1)通过敲除小鼠TGIF基因来表征TGIF的生物学功能,并从HPE表型的角度来观察TGIF缺陷对前脑和颅面结构发育的影响。(2)利用该模型,我们将研究TGIF在前脑结构发育中的潜在机制。我们将分析神经管,其中神经管图案在TGF-β缺陷小鼠。这两方面的研究将有助于阐明TGIF在小鼠发育中的作用,特别是其在HPE发病机制中的意义。
英文摘要
DESCRIPTION (provided by applicant): This is a R03 application focused on the initial characterization of TGIF knockout mice and the use of this mouse model to explore the potential link of TGIF to the defect in brain development, especially related to holoprosencephaly (HPE) disorder. HPE is a human genetic disease with characteristic defects in brain and craniofacial development. HPE is the most common structural defect of the developing forebrain in humans, and mutations have been found in genes that govern neural tube patterning in early brain development. TG-interacting factor (TGIF) is a homeobox protein that functions as a transcriptional co-repressor to modulate transforming growth factor beta (TGF-beta) induced gene transcription by direct association with Smad proteins. Mutations of TGIF have been found in HPE patients, indicating that TGIF may play an important role in forebrain development. Currently, the in vivo function of TGIF is unknown. In this proposal, we will employ the following two strategies to elucidate the biological function of TGIF in brain development: (1)We will characterize the biological function of TGIF by knockout of TGIF gene in mouse, then the effect of TGIF deficiency on the development of forebrain and craniofacial structures will be followed with regard to HPE phenotype. (2) Using this mouse model, we will study the potential mechanism underlying the function of TGIF in the development of forebrain structures. We will analyze the neural tube in which the neural tube patterning in TGIF-deficient mice. Taken together, the proposed studies in these two aspects will delineate the function of TGIF in mouse development, especially its implication in HPE pathogenesis.
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Analysis of brain development in TGIF deficient mouse
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