Zebrafish sall1a and sall4 contribute to body elongation

被引:0
作者
Kawakami, Hiroko [1 ,2 ,3 ]
Bailey, Abigail [1 ]
Gavin, Ella [1 ]
Gearhart, Micah D. [4 ]
Isabella, Adam J. [1 ,3 ]
Kawakami, Yasuhiko [1 ,2 ,3 ]
机构
[1] Univ Minnesota, Dept Genet Cell Biol & Dev, 321 Church St SE,6-160 Jackson Hall, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Stem Cell Inst, Minneapolis, MN USA
[3] Univ Minnesota, Dev Biol Ctr, Minneapolis, MN USA
[4] Univ Minnesota, Dept Obstet Gynecol & Womens Hlth, Minneapolis, MN USA
基金
美国国家卫生研究院;
关键词
Body/tail elongation; sall1a; sall4; POSTERIOR BODY; STEM-CELLS; SALL4; GENE; DIFFERENTIATION; PROLIFERATION; PROGENITORS; EXPRESSION; OXIDATION; TRUNK;
D O I
10.1016/j.ydbio.2025.06.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 postfertilization, 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.
引用
收藏
页码:185 / 193
页数:9
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