FRI-743 How Partially Redundant Genes Compensate for the Loss of their Partner: Examination of the Partially Redundant Roles of the Tbx8 and Tbx9 Genes in Embryonic Nematode Development

Friday, October 12, 2012: 10:40 PM
Hall 4E/F (WSCC)
Samuel Mullen , Biomedical Engineering, Johns Hopkins University, Baltimore, MD
Chau Huynh , Genome Science, University of Washington, Seattle
Robert Waterston , Genome Science, University of Washington, Seattle
Gene duplication is common in evolution, but we know little about the degree to which a duplicate gene can compensate for the loss of its counterpart. To study this we are looking at a duplicated gene found in C. elegans. The Tbx-8 and Tbx-9 genes encode Tbox transcription factors which affect embryonic development. Tbx-8 and Tbx-9 are are thought to be a result of a recent genetic duplication, because they reside in close proximity to one another in the genome, they encode proteins with 64% amino acid identity, they are largely redundant, and they are both expressed in precursor cells of the hypodermis and bodywall muscle. We hypothesize that tbx-8 can compensate for the loss of Tbx-9 by activating the expression of Tbx-8 in cells that normally express Tbx-9.To test this hypothesis, we generated a strain of C. elegans with a Tbx-8 promoter fusion to mCherry such that we can test whether tbx-8 promoter activity is altered in a tbx-9 or tbx-8 deletion background. By using confocal microscopy to image mCherry fluorescence during embryonic development, we anticipate that our studies will reveal how the expression of a partially redundant gene can change to compensate for loss of its counterpart.