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通过启动子捕获获得的秀丽隐杆线虫分化的分子标记。

Molecular markers of differentiation in Caenorhabditis elegans obtained by promoter trapping.

作者信息

Young J M, Hope I A

机构信息

Department of Pure and Applied Biology, University of Leeds, United Kingdom.

出版信息

Dev Dyn. 1993 Feb;196(2):124-32. doi: 10.1002/aja.1001960206.

Abstract

Differentiation of specific cell types during animal development can be detected by monitoring expression of appropriate genes. For this study, six different beta-galactosidase expression patterns which can be used as differentiation markers in the nematode Caenorhabditis elegans are described. An earlier promoter trap screen identified pools of recombinant plasmids which gave patterns of beta-galactosidase expression when used to transform C. elegans. Each recombinant plasmid contained a random fragment of C. elegans genomic DNA fused upstream of a promoterless lacZ gene. Six of these pools were chosen, and individual pattern-producing plasmids within these pools were identified. The expression patterns have been characterized more thoroughly than in the original screen, thereby providing molecular markers for differentiation of several cell types. Many of the expression patterns involve more than one cell type. The genomic origin of the inserts of active plasmids were determined through localization on the physical genome map.

摘要

在动物发育过程中,特定细胞类型的分化可以通过监测适当基因的表达来检测。在本研究中,描述了六种不同的β-半乳糖苷酶表达模式,它们可作为线虫秀丽隐杆线虫中的分化标记。早期的启动子陷阱筛选鉴定出了重组质粒库,当用于转化秀丽隐杆线虫时,这些质粒库呈现出β-半乳糖苷酶表达模式。每个重组质粒都包含一个秀丽隐杆线虫基因组DNA的随机片段,该片段融合在无启动子的lacZ基因上游。从这些库中选择了六个库,并鉴定了这些库中产生特定模式的单个质粒。与原始筛选相比,对表达模式进行了更全面的表征,从而为几种细胞类型的分化提供了分子标记。许多表达模式涉及不止一种细胞类型。通过定位在物理基因组图谱上确定了活性质粒插入片段的基因组来源。

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