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High Resolution Whole Mount In Situ Hybridization within Zebrafish Embryos to Study Gene Expression and Function
Published on: October 19, 2013
Zebrafish sall1a and sall4 contribute to body elongation
Hiroko Kawakami1, Abigail Bailey2, Ella Gavin2
1Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN, United States of America; Stem Cell Institute, University of Minnesota, Minneapolis, MN, United States of America; Developmental Biology Center, University of Minnesota, Minneapolis, MN, United States of America.
Abstract:
Vertebrate embryos elongate the body after gastrulation. Unlike in mice, which elongate both the trunk and tail after gastrulation, zebrafish embryos complete development of the trunk by the end of gastrulation, followed by tail elongation by proliferation of posteriorly located progenitors. Previous studies have shown that the transcription factors SALL1 and SALL4 redundantly regulate tail elongation in mouse embryos. To test whether sall1a and sall4 also regulate tail elongation in zebrafish, we generated zebrafish mutants for these genes. By 24 h post-fertilization, sall4 mutant embryos developed normally but exhibited changes in gene expression at the posterior end of the body. sall1a mutants also developed normally by 24 h post-fertilization. However, embryos mutant for both sall1a and sall4 showed a slight but significant reduction in body length compared to wild-type embryos. Our results support a role for sall1a and sall4 in tail elongation in zebrafish, though their contribution appears smaller than that observed in mouse embryos.
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