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通过单只小鼠原肠胚期胚胎前中内胚层之间的消减杂交分离新的cDNA。

Isolation of novel cDNAs by subtractions between the anterior mesendoderm of single mouse gastrula stage embryos.

作者信息

Shimono A, Behringer R R

机构信息

Department of Molecular Genetics, University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas, 77030, USA.

出版信息

Dev Biol. 1999 May 15;209(2):369-80. doi: 10.1006/dbio.1999.9256.

Abstract

The anterior mesendoderm of mid- to late primitive streak stage mouse embryos has the ability to induce anterior neuroectodermal fate in naive epiblast [S.-L. Ang and J. Rossant (1993) Development 118, 139-149]. A number of genes have been found to be expressed in this tissue, notably the transcription factor Lim1. Lim1-null mice have anterior mesendoderm defects that result in a lack of head formation. Thus, the anterior mesendoderm of gastrula stage mouse embryos should express Lim1-regulated genes that are essential for head development. To identify Lim1-regulated genes, a differential screen with subtraction was developed, using cDNA pools that were amplified from the anterior mesendoderm of single wild-type and Lim1-null gastrula stage embryos. This novel screen strategy has yielded 22 cDNAs that show differential expression between anterior mesendoderm cells of wild-type and Lim1-null embryos. The expression of one novel cDNA SII6 initially colocalizes with Lim1 in the anterior mesendoderm of gastrula stage embryos. Moreover, SII6 expression is undetectable in the anterior mesendoderm of Lim1-null embryos. This screen identifies a set of putative Lim1 target genes that may have important roles in vertebrate head formation. Furthermore, this differential screen strategy should provide a broadly applicable approach to identify differences in gene expression between embryonic tissues of limiting quantity.

摘要

原肠胚中期至后期小鼠胚胎的前中内胚层具有在未分化的上胚层中诱导前神经外胚层命运的能力[S.-L. 安和J. 罗桑特(1993年)《发育》118卷,139 - 149页]。已发现许多基因在该组织中表达,尤其是转录因子Lim1。Lim1基因敲除的小鼠存在前中内胚层缺陷,导致头部无法形成。因此,原肠胚期小鼠胚胎的前中内胚层应该表达对头部发育至关重要的Lim1调控基因。为了鉴定Lim1调控的基因,开发了一种减法差异筛选方法,使用从单个野生型和Lim1基因敲除的原肠胚期胚胎的前中内胚层扩增的cDNA文库。这种新颖的筛选策略产生了22个cDNA,它们在野生型和Lim1基因敲除胚胎的前中内胚层细胞之间表现出差异表达。一个新的cDNA SII6的表达最初在原肠胚期胚胎的前中内胚层中与Lim1共定位。此外,在Lim1基因敲除胚胎的前中内胚层中检测不到SII6的表达。该筛选鉴定出一组假定的Lim1靶基因,它们可能在脊椎动物头部形成中发挥重要作用。此外,这种差异筛选策略应该提供一种广泛适用的方法来鉴定有限数量胚胎组织之间的基因表达差异。

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