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foxj1xenopus esophagus 

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Experiment details for foxj1

Walentek P et al. (2015) Assay

ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles.

Gene Clone Species Stages Anatomy
foxj1.L laevis NF stage 45 esophagus

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  Fig. 5. foxj1 and atp4a are co-expressed in the gastrointestinal tract which transiently harbors motile cilia in the stomach. (A–F) WMISH for atp4a (A,C,D) and foxj1 (E,F) in the GI tract of stage 43–45 tadpoles (A–C, E; stomach highlighted by arrowheads; ventral views) and isolated GI tracts (D, F). (B) atp4a sense control revealed no staining. Note the co-expression of atp4a and foxj1 at stage 45 (C–F). (G–M) GI tract ciliation as shown by immunofluorescent staining of cilia/tubulin (acetylated-α-tubulin staining, red) and staining for actin (phalloidin, green) as well as nuclei (DAPI, blue) on cryosections from stage 45 tadpoles (planes indicated in J). MCCs (M) were found in the esophagus (es; G–I,K), stomach (sto; G–I,L) and the proximal part of the small intestine (smi; H, I). (N, N`) Scanning electron microscopy analysis of gastric epithelia from adult frogs revealed the presence of short monocilia, but lack of MCCs. (O) Injection of atp4aSplMO targeted to the endoderm prevented normal development of the GI tract. Targeting was monitored by co-injection of fluorescent rhodamine dextrane (red). Embryos are shown in ventral view. a, anterior; d, dorsal; es, esophagus; l, left; p, posterior; r, right; st., stage; smi, small intestine; sto, stomach; v, ventral.