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利用裂殖酵母粟酒裂殖酵母中经染色体标记的绿色荧光蛋白融合文库对基因产物进行定位。

Localization of gene products using a chromosomally tagged GFP-fusion library in the fission yeast Schizosaccharomyces pombe.

作者信息

Hayashi Aki, Ding Da-Qiao, Tsutsumi Chihiro, Chikashige Yuji, Masuda Hirohisa, Haraguchi Tokuko, Hiraoka Yasushi

机构信息

Kobe Advanced ICT Research Center, National Institute of Information and Communications Technology, Japan.

出版信息

Genes Cells. 2009 Feb;14(2):217-25. doi: 10.1111/j.1365-2443.2008.01264.x. Epub 2008 Jan 12.

Abstract

We constructed a library of chromosomally-tagged green fluorescent protein (GFP) fusions in the fission yeast Schizosaccharomyces pombe. This library contains 1058 strains. In each strain, the coding sequence of GFP is integrated at the 3'-end of a particular chromosomal ORF such that the full-length GFP fusion construct is expressed under the control of the original promoter. Integration of the GFP coding sequence at the authentic chromosomal location of each gene was confirmed by PCR. Microscopic screening of these strains detected sufficient levels of GFP signal in 710 strains and allowed assignment of these GFP-fusion gene products with their intracellular localization: 374 proteins were localized in the nucleus, 65 proteins in the nucleolus, 34 proteins at the nuclear periphery, 27 proteins at the plasma membrane and cytoplasmic membranous structures, 24 proteins at the spindle pole body and microtubules, 92 proteins at cytoplasmic structures, and 94 proteins were uniformly distributed throughout the cytoplasm.

摘要

我们构建了一个裂殖酵母粟酒裂殖酵母中带有染色体标签的绿色荧光蛋白(GFP)融合文库。该文库包含1058个菌株。在每个菌株中,GFP的编码序列整合到特定染色体ORF的3'末端,使得全长GFP融合构建体在原始启动子的控制下表达。通过PCR确认了GFP编码序列在每个基因的真实染色体位置上的整合。对这些菌株进行显微镜筛选,在710个菌株中检测到足够水平的GFP信号,并确定了这些GFP融合基因产物的细胞内定位:374种蛋白质定位于细胞核,65种蛋白质定位于核仁,34种蛋白质定位于核周边,27种蛋白质定位于质膜和细胞质膜结构,24种蛋白质定位于纺锤极体和微管,92种蛋白质定位于细胞质结构,94种蛋白质均匀分布于整个细胞质中。

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