Abstract
We present here the results of forward and reverse genetic screens for chemically-induced mutations in Xenopus tropicalis. In our forward genetic screen, we have uncovered 77 candidate phenotypes in diverse organogenesis and differentiation processes. Using a gynogenetic screen design, which minimizes time and husbandry space expenditures, we find that if a phenotype is detected in the gynogenetic F2 of a given F1 female twice, it is highly likely to be a heritable abnormality (29/29 cases). We have also demonstrated the feasibility of reverse genetic approaches for obtaining carriers of mutations in specific genes, and have directly determined an induced mutation rate by sequencing specific exons from a mutagenized population. The Xenopus system, with its well-understood embryology, fate map, and gain-of-function approaches, can now be coupled with efficient loss-of-function genetic strategies for vertebrate functional genomics and developmental genetics. © 2006 Goda et al.
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CITATION STYLE
Goda, T., Abu-Daya, A., Carruthers, S., Clark, M. D., Stemple, D. L., & Zimmerman, L. B. (2006). Genetic screens for mutations affecting development of Xenopus tropicalis. PLoS Genetics, 2(6), 0811–0825. https://doi.org/10.1371/journal.pgen.0020091
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