FIGURE SUMMARY
Title

TFAP2B Haploinsufficiency Impacts Gastrointestinal Function and Leads to Pediatric Intestinal Pseudo-obstruction

Authors
Zada, A., Kuil, L.E., de Graaf, B.M., Kakiailatu, N., Windster, J.D., Brooks, A.S., van Slegtenhorst, M., de Koning, B., Wijnen, R.M.H., Melotte, V., Hofstra, R.M.W., Brosens, E., Alves, M.M.
Source
Full text @ Front Cell Dev Biol

(Continued).

TFAP2B transcript and protein expression analysis. (A) qRT-PCR analysis of TFAP2B transcript levels of WT, c.706 C > T, c.898 C > T, c.1144 C > T, and exon 4 deletion expression constructs show no statistically significant difference among the samples normalized to GAPDH and b-Actin. (B) Western blot analysis of all tested variants shows absence of protein products for the syndromic craniosynostosis variant (c.1144 C > T) and PIPO variant (del Exon 4). Protein products are still detectable for the Char syndrome variants (c.706 C > T and c.898 C > T). A Myc-tag antibody was used to visualize TFAP2B protein levels.

Decreased enteric neuronal numbers and delayed intestinal transit time in tfap2b +/− zebrafish. (A) Image of the zebrafish wild type, tfap2b +/− and tfap2 −/− intestine. Enteric neurons are shown in green and a white dash line delineates the intestine. (B) A significant reduced number of enteric neurons (*p < 0.0001, unpaired t-test) was found in the tfap2b +/− fish (n = 20) when compared to the wild type fish (n = 11). Neurons were counted and presented per 100 µm. Four out of 7 tfap2b −/− fish showed total aganglionosis. (C) Intestinal transit time was determined by the presence of a fluorescent pellet (red fluorescent) in the intestine 16 h after food intake (final measurement). To help evaluation, the zebrafish intestine was divided in 4 zones, proximal to distal, and empty. Only fish with fluorescent pellet in zone 1 at time 0 (initial measurement), were selected for this study. (D) A significant delay in intestinal transit time was observed in tfap2b +/− fish, as 75% of wild type fish had an empty intestine 16 h after food intake, in comparison with only 38.4% of tfap2b +/− fish (p < 0.0001, Proportion test). All tfap2b −/− fish had pellet retained in zone 2. (E) No difference in the ratio total body length to mouth-distal intestinal length was identified for wild type, tfap2b+/− and tfap2b−/− fish.

Expression levels of tfap2b and ednrbb during zebrafish development. (A) Expression levels of tfap2b in crispant fish at 8 hpf, 1, 2, 3, 4, and 5 dpf show a significant decrease when compared to wild type, starting from 1 dpf onwards (p < 0.05, unpaired t-test). (B) Expression levels of ednrbb in tfap2b crispants show a significant decrease when compared to wild type fish, at 4 and 5 dpf (p < 0.05, unpaired t-test).

EXPRESSION / LABELING:
Genes:
Fish:
Knockdown Reagent:
Anatomical Term:
Stage Range: 75%-epiboly to Day 5
PHENOTYPE:
Fish:
Knockdown Reagent:
Observed In:
Stage Range: Prim-5 to Day 5

Differentiated enteric neurons in tfap2b +/− fish. (A) Confocal microscope images of HuC/HuD and phox2bb:GFP positive cells in wild type and tfap2b +/− F2 fish. (B) No significant difference in the ratio of HuC/HuD and phox2bb:GFP positive cells in wild type and tfap2b +/− F2 fish was found (p > 0.05, unpaired t-test).

Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Front Cell Dev Biol