Concerted Assembly and Cloning of Multiple DNA Segments Using In Vitro Site-Specific Recombination: Functional Analysis of Multi-Segment Expression Clones

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 4
Figure 4

Functional analysis of transcriptional fusions. (A) Promoter-eGFP fusions and (B) promoter-STE2 receptor fusions in yeast cells co-transformed with the FUS1-yeGFP reporter. Relative GFP fluorescence was measured over a 16-h period. Yeast strains were assayed in the presence (filled symbols) or absence (open symbols) of 500 nM α-factor as described in the Methods. Promoter fusions are as follows: STE2 (Red), ADH1 (yellow), GPD1 (blue), TEF2 (green), and CUP1 (black). Yeast strains containing the CUP1 promoter fusions were assayed in the presence (black circles) and absence (black squares) of 100 μM copper sulfate.

This Article

  1. Genome Res. 14: 2111-2120

Preprint Server