AI Article Synopsis

  • A library of 1,058 strains of fission yeast was created, each with a genetically tagged green fluorescent protein (GFP) fusion integrated at the end of specific genes, allowing for the study of protein localization.
  • Each GFP fusion is controlled by the original promoter of the gene to ensure proper expression, with integration confirmed via PCR.
  • Microscopic analysis identified the intracellular locations of GFP signals in 710 strains, revealing diverse distributions, including 374 proteins in the nucleus and 94 uniformly distributed in the cytoplasm.

Article 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.

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Source
http://dx.doi.org/10.1111/j.1365-2443.2008.01264.xDOI Listing

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