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. 2019 Sep 3;17(9):e3000087. doi: 10.1371/journal.pbio.3000087

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© 2019 Serrano et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 4 — (A-B) Ventral view of vasculature in wild-type tg(kdrl:GFP) sibling (A) and kmt2d^zy59;tg(kdrl:GFP) mutants at 5 dpf. Cephalic vascular architecture in kmt2d^zy59 embryos was abnormal with reduced elongation in the anteroposterior body axis, loss of bilateral symmetry, and reduced HA (A, B). In kmt2d^zy59 mutants, AA1 (A, B) was shorter with minimum elongation towards the anterior area of the embryo, the AA3 (A, B) was rudimentary,whereas AA4−6 were reduced or absent (A, B). Mouth and eyes in kmt2d^zy59 showed primitive characteristics with differences in the thickness of the OV in particular (A–B). Note the abnormal endocardial component of the heart (A, B; he). Aʹ and B are simplified cartoons of the main differences in the AAs development in wild-type (Aʹ) and mutant (Bʹ) backgrounds. Branchial vasculature loops were removed to allow better visualization of aortic arch points of origin. (C-D) Lateral view of cephalic vasculature in wild-type tg(kdrl:GFP) sibling and kmt2d^zy59;tg(kdrl:GFP) mutants at 7 dpf. kmt2d^zy59 exhibited a complete absence of the vascular loops associated with AAs 3–6 with only a rudiment of the AA3 present (D, AA*). The general cranial vascular network was mispatterned with a particular strong impact in the CtA, ACeV, and VA (D; in orange). In kmt2d^zy59 mutant, most vessels had reduced lumens with the exception of the NCA (C, D), DVC (C, F) and IOC (C, F) that show thicker vessel diameter. Note the reduced HA from a lateral view (D, HA in orange; scale bars = 100 μm). (E) Cell cycle profile analysis by FACS for 7 individual embryos per genotype at 7 dpf. The gates set up for nuclear staining (DAPI) in kdrl positive cells (endothelial and endocardial cells) are shown. (F) Cell cycle profiles for Kdrl positive cells in kmt2d^zy59 mutants showed no significant difference in the percentage of G2/M cells at 3 dpf. In contrast, at 7 dpf, there was a significant decrease in number of dividing cells in kmt2d^zy59 mutants when compared with wild-type siblings. Unpaired two-tailed t test, p = 0.407 n.s. for 3 dpf; p = 0.0002 for 7 dpf, n = 7 per genotype. Values for each data point can be found in S1 Data. AA, aortic arch; AA1, mandibular arch; AA2, hyoid arch; AA3, first branchial arch; AA4, second branchial arch; AA5 third branchial arch; AA6, fourth branchial arch; ACeV, anterior cerebral vein; CtA, central artery; DCV, dorsal ciliary vein; DLV, dorsal longitudinal vein; dpf, days post fertilization; ey, eye; FACS, fluorescent activated cell sorting; GFP, green fluorescent protein; HA, hypobranchial artery; kdrl, kinase insert domain receptor like; IOC, inner optic circle; MsV, mesencephalic vein; NCA, nasal ciliary artery; ORA, opercular artery; OV, optic vein; VA, ventral aorta.