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平面细胞极性基因在小鼠中枢神经系统发育过程中的表达。

Expression of planar cell polarity genes during development of the mouse CNS.

作者信息

Tissir Fadel, Goffinet André M

机构信息

Developmental Neurobiology Unit, University of Louvain Medical School, 73, Av. E. Mounier, Box DENE7382, B1200 Brussels, Belgium.

出版信息

Eur J Neurosci. 2006 Feb;23(3):597-607. doi: 10.1111/j.1460-9568.2006.04596.x.

Abstract

Atypical cadherin (Celsr3) and the receptor Frizzled3 (Fzd3) are crucial for the development of axonal tracts in the mouse CNS. Celsr3 and Fzd3 are orthologues of the Drosophila'planar cell polarity' (PCP) genes flamingo/starry night (fmi/stan) and frizzled, respectively. Reasoning that Celsr3 and Fzd3 might interact with PCP orthologues in mammals like they do in flies, we used mRNA in situ hybridization to compare the expression of Celsr3 and Fzd3 with that of dishevelled 1, 2 and 3 (Dvl1-3), van gogh-like 1 and 2 (Vangl1, 2), and prickle-like 1 and 2 (Prickle1, 2), during mouse CNS development, from embryonic day 10.5 to postnatal day 21. With the relative exception of Vangl1, all genes were expressed in the developing CNS. Although Celsr3- and Fzd3-deficient mice have similar phenotypes, Fzd3 expression was more widespread than that of Celsr3. Vangl2 and Dvl2 were preferentially expressed in ventricular zones, in keeping with their role during neural tube closure, where they could be partners of Celsr1. Dvl1 had a broad expression, reminiscent of that of Celsr2, and may be involved in neural maintenance. A large overlap in the expression territories of Dvl genes suggested redundancy. Vangl1 and Prickle1 had expression canvases different from each other and from other candidates, indicating unrelated function. Like Celsr3, Dvl3 and Prickle2 were expressed more strongly in postmitotic neurons than in precursors. Thus, the analogy between the PCP and Celsr3-Fzd3 genetic networks is limited, but may include Dvl3 and/or Prickle2.

摘要

非典型钙黏蛋白(Celsr3)和受体卷曲蛋白3(Fzd3)对小鼠中枢神经系统轴突束的发育至关重要。Celsr3和Fzd3分别是果蝇“平面细胞极性”(PCP)基因火烈鸟/星夜(fmi/stan)和卷曲蛋白的直系同源物。鉴于Celsr3和Fzd3可能像在果蝇中那样与哺乳动物中的PCP直系同源物相互作用,我们使用mRNA原位杂交技术,比较了从胚胎第10.5天到出生后第21天小鼠中枢神经系统发育过程中Celsr3和Fzd3与蓬乱蛋白1、2和3(Dvl1 - 3)、类梵高蛋白1和2(Vangl1、2)以及棘状蛋白1和2(Prickle1、2)的表达情况。除了Vangl1相对例外之外,所有基因都在发育中的中枢神经系统中表达。尽管Celsr3和Fzd3基因缺陷小鼠具有相似的表型,但Fzd3的表达比Celsr3更广泛。Vangl2和Dvl2优先在脑室区表达,这与它们在神经管闭合过程中的作用一致,在那里它们可能是Celsr1的伙伴。Dvl1具有广泛的表达,让人联想到Celsr2的表达情况,并且可能参与神经维持。Dvl基因表达区域有很大重叠,表明存在冗余。Vangl1和Prickle1的表达范围彼此不同,也与其他候选基因不同,表明功能不相关。与Celsr3一样,Dvl和Prickle2在有丝分裂后神经元中的表达比在前体细胞中更强。因此,PCP与Celsr3 - Fzd3遗传网络之间的类比是有限的,但可能包括Dvl3和/或Prickle2。

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