Visualization of C. elegans transgenic arrays by GFP

Background: Targeting the green fluorescent protein (GFP) via the E. coli lac repressor (Lacl) to a specific DNA sequence, the lac operator (lac0), allows visualization of chromosomes in yeast and mammalian cells. In principle this method of visualization could be used for genetic mosaic analysis, which requires cell-autonomous markers that can be scored easily and at single cell resolution. The C. elegans lin-3 gene encodes an epidermal growth factor family (EGF) growth factor. lin-3 is expressed in the gonadal anchor cell and acts through LET-23 (transmembrane protein tyrosine kinase and ortholog of EGF receptor) to signal the vulval precursor cells to generate vulval tissue. lin-3 is expressed in the vulval cells later, and recent evidence raises the possibility that lin-3 acts in the vulval cells as a relay signal during vulval induction. It is thus of interest to test the site of action of lin-3 by mosaic analysis. Results: We visualized transgenes in living C. elegans by targeting the green fluorescent protein (GFP) via the E. coli lac repressor (Lacl) to a specific 256 sequence repeat of the lac operator (lac0) incorporated into transgenes. We engineered animals to express a nuclear-localized GFP-Lacl fusion protein. C. elegans cells having a lac0 transgene result in nuclear-localized bright spots (i. e., GFP-Lacl bound to lac0). Cells with diffuse nuclear fluorescence correspond to unbound nuclear localized GFP-Lacl. We detected chromosomes in living animals by chromosomally integrating the array of the lac0 repeat sequence and visualizing the integrated transgene with GFP-Lacl. This detection system can be applied to determine polyploidy as well as investigating chromosome segregation. To assess the GFP-Lacl center dot lac0 system as a marker for mosaic analysis, we conducted genetic mosaic analysis of the epidermal growth factor lin-3, expressed in the anchor cell. We establish that lin-3 acts in the anchor cell to induce vulva development, demonstrating this method's utility in detecting the presence of a transgene. Conclusion: The GFP-Lacl center dot lac0 transgene detection system works in C. elegans for visualization of chromosomes and extrachromosomal transgenes. It can be used as a marker for genetic mosaic analysis. The lac0 repeat sequence as an extrachromosomal array becomes a valuable technique allowing rapid, accurate determination of spontaneous loss of the array, thereby allowing high-resolution mosaic analysis. The lin-3 gene is required in the anchor cell to induce the epidermal vulval precursors cells to undergo vulval development.