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一项用于鉴定参与果蝇胚胎发育的分泌蛋白和跨膜蛋白的高通量筛选。

A high throughput screen to identify secreted and transmembrane proteins involved in Drosophila embryogenesis.

作者信息

Kopczynski C C, Noordermeer J N, Serano T L, Chen W Y, Pendleton J D, Lewis S, Goodman C S, Rubin G M

机构信息

Department of Molecular and Cell Biology, Howard Hughes Medical Institute, University of California, Berkeley, CA 94720-3200, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9973-8. doi: 10.1073/pnas.95.17.9973.

Abstract

Secreted and transmembrane proteins play an essential role in intercellular communication during the development of multicellular organisms. Because only a small number of these genes have been characterized, we developed a screen for genes encoding extracellular proteins that are differentially expressed during Drosophila embryogenesis. Our approach utilizes a new method for screening large numbers of cDNAs by whole-embryo in situ hybridization. The cDNA library for the screen was prepared from rough endoplasmic reticulum-bound mRNA and is therefore enriched in clones encoding membrane and secreted proteins. To increase the prevalence of rare cDNAs in the library, the library was normalized using a method based on cDNA hybridization to genomic DNA-coated beads. In total, 2,518 individual cDNAs from the normalized library were screened by in situ hybridization, and 917 of these cDNAs represent genes differentially expressed during embryonic development. Sequence analysis of 1,001 cDNAs indicated that 811 represent genes not previously described in Drosophila. Expression pattern photographs and partial DNA sequences have been assembled in a database publicly available at the Berkeley Drosophila Genome Project website (). The identification of a large number of genes encoding proteins involved in cell-cell contact and signaling will advance our knowledge of the mechanisms by which multicellular organisms and their specialized organs develop.

摘要

分泌蛋白和跨膜蛋白在多细胞生物发育过程中的细胞间通讯中起着至关重要的作用。由于这些基因中只有少数已被表征,我们开发了一种筛选方法,用于筛选在果蝇胚胎发育过程中差异表达的编码细胞外蛋白的基因。我们的方法利用了一种通过全胚胎原位杂交筛选大量cDNA的新方法。用于筛选的cDNA文库是由与糙面内质网结合的mRNA制备的,因此富含编码膜蛋白和分泌蛋白的克隆。为了提高文库中稀有cDNA的比例,使用基于cDNA与基因组DNA包被珠子杂交的方法对文库进行了标准化。总共通过原位杂交筛选了来自标准化文库的2518个单个cDNA,其中917个cDNA代表在胚胎发育过程中差异表达的基因。对1001个cDNA的序列分析表明,811个代表果蝇中以前未描述的基因。表达模式照片和部分DNA序列已组装在伯克利果蝇基因组计划网站()上公开可用的数据库中。大量编码参与细胞间接触和信号传导的蛋白质的基因的鉴定将推动我们对多细胞生物及其特化器官发育机制的认识。

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