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发育中的后脑的分级视黄酸反应。

Graded retinoid responses in the developing hindbrain.

作者信息

Godsave S F, Koster C H, Getahun A, Mathu M, Hooiveld M, van der Wees J, Hendriks J, Durston A J

机构信息

Netherlands Institute for Developmental Biology, Utrecht.

出版信息

Dev Dyn. 1998 Sep;213(1):39-49. doi: 10.1002/(SICI)1097-0177(199809)213:1<39::AID-AJA4>3.0.CO;2-Z.

Abstract

The purpose of this study was to make an explicit test of the idea that a retinoid could act as a morphogen, differentially activating genes and specifying anteroposterior (a-p) level in the developing vertebrate central nervous system (CNS). Our approach was to characterize the concentration-dependent effects of retinoic acid (RA) on the neural expression of a set of a-p patterning genes, both in vivo and in an in vitro system for neural patterning. Our results indicate that a retinoid is unlikely to specify a-p level along the entire CNS. Instead, our data support the idea that the developing hindbrain may be patterned by a retinoid gradient. Sequentially more posterior hindbrain patterning genes were induced effectively by sequentially higher RA concentration windows. The most posterior CNS level induced under our RA treatment conditions corresponded to the most posterior part of the hindbrain.

摘要

本研究的目的是对类视黄醇可作为形态发生素,在发育中的脊椎动物中枢神经系统(CNS)中差异激活基因并指定前后(a-p)水平这一观点进行明确验证。我们的方法是在体内和用于神经模式形成的体外系统中,表征视黄酸(RA)对一组a-p模式形成基因的神经表达的浓度依赖性影响。我们的结果表明,类视黄醇不太可能沿整个中枢神经系统指定a-p水平。相反,我们的数据支持这样一种观点,即发育中的后脑可能由类视黄醇梯度形成模式。依次更高的RA浓度窗口有效地诱导了依次更靠后的后脑模式形成基因。在我们的RA处理条件下诱导的最靠后的中枢神经系统水平对应于后脑的最后部分。

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