fn1abns692 mutants also display a variable cardiac phenotype. (A) Schematic showing the WT, natter/tl43c, and bns692 fn1a alleles. Exons (n = 46) are indicated by black boxes. The start codons are represented by a green triangle and the stop codons by a red octagon. (B)In situ hybridisation with the myocardial marker myl7 was performed on 24 hpf fn1abns692 mutant embryos and WT siblings from four single pair fn1abns692 heterozygous intercrosses. The proportion of embryos matching the image shown is indicated in the top right corner of each image. The remaining 5/49 mutant embryos displayed a linear heart tube phenotype as noted in (C). Dorsal views are shown with anterior to the top. (C) Quantification of the 24 hpf myocardial migration phenotype in fn1abns692 mutants and WT siblings shown in (B). (D) Quantification of the 100 hpf cardiac phenotype in fn1abns692 mutants and WT siblings from three single pair fn1abns692 heterozygous intercrosses. The numbers on each bar in (C) and (D) indicate the total number of larvae assessed. All p-values were calculated using chi-squared tests. Scale bars, 100 µm.
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