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vax2xenopus   

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Experiment details for vax2

Liu M et al. (2008) Assay

A role for Xvax2 in controlling proliferation of Xenopus ventral eye and brain progenitors.

Gene Clone Species Stages Anatomy
vax2.L laevis NF stage 22 to NF stage 27 optic vesicle
vax2.L laevis NF stage 32 olfactory placode , telencephalon , optic vesicle
vax2.L laevis NF stage 35 and 36 olfactory placode , telencephalon
vax2.L laevis NF stage 46 ciliary marginal zone , retinal outer nuclear layer , retinal inner nuclear layer , retinal ganglion cell layer

  Figure 1. A-L: Expression of Xvax2 as detected by immunohistochemistry (A-D,J-L) and in situ hybridization (E-I) on whole embryos (A-H) and coronal sections of eye (I-L) of Xenopus laevis. The developmental stages (St.) are indicated in each panel. Whole embryos are shown as anterior views, and the sections with dorsal side up. op, olfactory placode; pos, presumptive optic stalk; vov, ventral optic vesicle; voc, ventral optic cup; vt, ventral telencephalon; CMZ, ciliary marginal zone; GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer. Scale bars = 100 mu m.

Gene Clone Species Stages Anatomy
vax2.L laevis NF stage 46 retinal outer nuclear layer , retinal inner nuclear layer , retinal ganglion cell layer

  Figure 3. A-C: Double staining for bromodeoxyuridine (BrdU) incorporation (red) and Xvax2 expression in the ventral CMZ of Xenopus retina (A,B) and the ventricular zone of brain (C) at st. 46. Location of Xvax2 mRNA (A) and protein (B,C) is shown in blue and green as detected by in situ hybridization and immunohistochemistry, respectively. D: A schematic model of the CMZ subdivision in Xenopus retina. Zone I, II-III and IV-V represent stem cells, proliferating retinoblasts, and postmitotic cells, respectively (Ohnuma S, et al.,[2002], reproduced with permission of the Company of Biologists). E-J: Analysis of cell cycle activity in the control (Ctrl) and 50 pg Xvax2-injected (Inj) side of Xenopus embryos as detected by immunohistochemistry (E-G,J) and in situ hybridization (H,I). Cell cycle activity (red) was detected by BrdU incorporation (E), anti-phosphohistone-H3 (F-G,J) and cyclinD1 expression (H, I) on coronal sections of eye (E-I) and forebrain (E,J) at st. 35 and st. 42. Cell nuclei are shown in blue by Hoechst staining (E-G,J). K,L: Gain-/loss-of-functional effects of Xvax2 on clonal sizes of retinal cells. The fluorescent image shows lipofected cells in retinal sections at stage 42, after transfection of GFP (K1) or cotransfection of GFP with Xvax2 (V2) construct Xvax2 (K2), Xvax2-VP16 (K3), Xvax2-EnR (K4) at st.17/18. L: Quantification of retinal clonal size is shown. Error bars represent standard error of the mean (SEM). Clone counts are indicated on each column. CMZ, ciliary marginal zone; ONL, outer nuclear layer; INL, inner nuclear layer; GCL, ganglion cell layer; Scale bars = 100 mu m.

Gene Clone Species Stages Anatomy
vax2.L laevis adult frog stage hypophysis , optic nerve , cerebellum , olfactory region , retinal outer nuclear layer , [+]

  Figure 2. A-L: Expression of Xvax2 as detected by in situ hybridization (A-G) and immunohistochemistry (H-L) in the adult Xenopus retina (F-I) and brain (A-E,J-L). Xvax2 mRNA localization (indicated by arrows) was detected on serial transversal sections of adult Xenopus brain at different anteroposterior levels (A-D) or on sagittal sections near the midline (E,J-L). F and G show the dorsal and ventral parts of coronal sections of the adult retina, respectively. H and I show sections corresponding to F and G, respectively. Cb, Cerebellum; Hy, hypophysis; HV, hypothalamic ventricle; LV, lateral ventricle; Se, Septum; OB, olfactory bulb; OT, optic tract; GCL, ganglion cell layer; INL, inner nuclear layer; ONL, outer nuclear layer. Scale bars = 100 mu m.