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Six3基因失活导致哺乳动物间脑出现渐进性尾化和异常模式形成。

Six3 inactivation causes progressive caudalization and aberrant patterning of the mammalian diencephalon.

作者信息

Lavado Alfonso, Lagutin Oleg V, Oliver Guillermo

机构信息

Department of Genetics and Tumor Cell Biology, St Jude Children's Research Hospital, 332 N. Lauderdale, Memphis, TN 38105-2794, USA.

出版信息

Development. 2008 Feb;135(3):441-50. doi: 10.1242/dev.010082. Epub 2007 Dec 19.

Abstract

The homeobox gene Six3 represses Wnt1 transcription. It is also required in the anterior neural plate for the development of the mammalian rostral forebrain. We have now determined that at the 15- to 17-somite stage, the prospective diencephalon is the most-anterior structure in the Six3-null brain, and Wnt1 expression is anteriorly expanded. Consequently, the brain caudalizes, and at the 22- to 24-somite stage, the prospective thalamic territory is the most-anterior structure. At around E11.0, the pretectum replaces this structure. Analysis of Six3;Wnt1 double-null mice revealed that Six3-mediated repression of Wnt1 is necessary for the formation of the rostral diencephalon and that Six3 activity is required for the formation of the telencephalon. These results provide insight into the mechanisms that establish anteroposterior identity in the developing mammalian brain.

摘要

同源框基因Six3可抑制Wnt1转录。在哺乳动物前脑发育过程中,前神经板也需要Six3。我们现已确定,在15至17体节期,Six3基因敲除小鼠的大脑中,预期的间脑是最靠前的结构,而Wnt1的表达向前扩展。因此,大脑发生尾化,在22至24体节期,预期的丘脑区域成为最靠前的结构。在大约E11.0时,顶盖前区取代了该结构。对Six3;Wnt1双基因敲除小鼠的分析表明,Six3介导的对Wnt1的抑制作用对于喙端间脑的形成是必需的,而Six3的活性对于端脑的形成也是必需的。这些结果为深入了解发育中的哺乳动物大脑建立前后身份的机制提供了线索。

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