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Fig. 3

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ZDB-IMAGE-111019-19
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Figures for Hinits et al., 2011
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Figure Caption

Fig. 3 Muscle growth is impaired in myodfh261 mutants. In situ mRNA hybridization for miR-206, myog and myhz1 and immunodetection of MyHC. Lateral (A,C,D) views, anterior to left or transverse cryosections (B). A. miR-206 in sequence-genotyped 48 hpf embryos from a myod+/fh261 incross is primarily in fast fibres and is strongly reduced. B. Embryos from A were sectioned and stained with MyHC. miR-206 expression is strongly reduced in myodfh261 mutants compared with their siblings, while MyHC immunodetection is only mildly reduced. C. At 72 hpf, miR-206 has increased in myod morphants, but is still less than in siblings. D. Compared to sibs, myodfh261 mutants (identified by head muscle defects) had less myog mRNA (arrowheads) and reduction in dorsoventral extent of somitic miR-206 and myhz1 mRNA (brackets). E. Somite volume increases with age, but is reduced in myodfh261 mutant. These differences were consistent in live and fixed embryos. Number of embryos per condition is shown on columns and t-test statistics are indicated above columns. F. Adult fish mass and length. Bars = 100 μm.

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Reprinted from Developmental Biology, 358(1), Hinits, Y., Williams, V.C., Sweetman, D., Donn, T.M., Ma, T.P., Moens, C.B., and Hughes, S.M., Defective cranial skeletal development, larval lethality and haploinsufficiency in Myod mutant zebrafish, 102-12, Copyright (2011) with permission from Elsevier. Full text @ Dev. Biol.