Abstract
A method to rapidly generate gene replacement constructs by fusion PCR is described for Aspergillus nidulans. The utility of the approach is demonstrated by green fluorescent protein (GFP) tagging of A. nidulans ndc80 to visualize centromeres through the cell cycle. The methodology makes possible large-scale GFP tagging, promoter swapping, and deletion analysis of A. nidulans.
Original language | English |
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Pages (from-to) | 1359-1362 |
Number of pages | 4 |
Journal | Eukaryotic Cell |
Volume | 3 |
Issue number | 5 |
DOIs | |
Publication status | Published - 1 Oct 2004 |
Externally published | Yes |
ASJC Scopus subject areas
- Microbiology
- Molecular Biology