|
Display additional annotations [+]
|
| |
Fig. 6. Otx2 confers the ability to activate FoxE3 in response to Notch signaling. (A-C′) Expression of Otx2 in the anterior ectoderm detected by in situ hybridization. At the neural plate stages, Otx2 is expressed in the anterior ectoderm including the presumptive lens-fields, which are circled with white dotted lines in A. Arrows in B indicate broad expression in the ectoderm that overlies the optic vesicles (ov) and surrounds the cement gland primordium (cg). Arrows in C indicate the border of ectodermal Otx2 expression. White lines in C indicate the planes of transverse sections shown in C′ and C′. Arrows in C′ and C′, respectively, indicate expression in the PLE overlying the optic vesicle and in the ectoderm overlying the forebrain. (D-H) Notch-Otx2 combination activates FoxE3 in the trunk ectoderm. Xenopus embryos injected with the mRNAs indicated in each panel were induced with Dex, and then subjected to lacZ staining and in situ hybridization with FoxE3 probe. Ectopic FoxE3 expression was not detected in embryos injected with mRNA encoding GR-Su(H)VP16 (1000 pg) (D), Otx2-GR (250 pg) (E), or NICD (1000 pg) (G), whereas it was detected in embryos injected with both GR-Su(H)VP16 (750 pg) and Otx2-GR (250 pg) (F), or both NICD (750 pg) and Otx2-GR (250 pg) (H). Arrowheads in F and H indicate ectopic FoxE3 expression. Arrows indicate endogenous FoxE3 expression in the PLE. The white line in F indicates the plane of the transverse section shown in the inset. Black arrowheads in the inset indicate the overlap of FoxE3 expression and nuclear lacZ staining in the ectodermal cells, and white arrowheads indicate cells in the underlying mesoderm layer showing nuclear lacZ staining but no FoxE3 expression. (I,J) The injected and uninjected sides, respectively, of an embryo injected with mRNA encoding GR-Otx2-En (250 pg), induced with Dex from stage 18, and then subjected to lacZ staining and in situ hybridization with FoxE3 probe at stage 22. Arrows indicate the PLE. (K) Transgenic experiments using Otx-Su(H) reporter constructs. Numbers of embryos with GFP expression in the PLE and the total number of normally (or near normally) developing embryos injected with the constructs shown on the left are indicated on the right-hand side with percentages of the GFP-positive cases. Gray and red boxes indicate Otx- and Su(H)-binding motifs, respectively, in the constructs, and crosses indicate base-substitution mutations introduced there. (L,L′) A representative transgenic embryo generated with Otx-Su(H)-βGFP. Black and white arrows indicate GFP expression in the eye and spinal cord, respectively. The white line indicates the plane of the transverse eye section shown in L′. Black and white arrowheads indicate GFP expression in the PLE and optic vesicle, respectively. |
|
|
| |
Fig. 1. In vivo deletion analysis identifies a 901 bp enhancer that directs PLE-specific expression of FoxE3. (A) FoxE3 expression in X. tropicalis embryos (stage 23) detected by in situ hybridization. (B-G) GFP expression detected by in situ hybridization in representative transgenic embryos (stages 22-24) generated with the reporter constructs shown to the left. White and black arrows in A-G indicate the PLE. The arrowhead in B indicates ectopic GFP expression in the presumptive oral ectoderm. Numbers of embryos with GFP expression in the PLE and the total number of normally (or near normally) developing embryos injected with each construct are indicated to the right, along with the percentage of GFP-positive cases. The 901 bp element necessary for PLE-specific expression is boxed with a dotted red line. *The expression in D was positive in the PLE but very spotty and broad, as shown in the left-hand panel. |
|
Display additional annotations [+]
|
| |
Fig. 5. Effects of manipulation of Notch signaling on FoxE3 expression and subsequent lens placode formation. (A,B) Frontal view of Xenopus embryos injected with mRNA encoding Delta2Tr (500 pg), fixed at stage 23, and subjected to lacZ staining (magenta) and in situ hybridization with FoxE3 or Rx probe (purple or deep purple staining). White and black arrowheads in A-H indicate in situ hybridization signals on injected and uninjected sides of embryos, respectively. (C,D,F,G) The injected and uninjected sides of embryos injected with Delta2Tr mRNA, fixed at stages 29/30, and hybridized with γ1-crystallin or Rx probe. (H) A transverse head section of the embryo shown in F,G. (E) The injected side of an embryo injected with both Delta2Tr mRNA (500 pg) and wild-type Delta2 mRNA (500 pg), fixed at stage 29, and hybridized with γ1-crystallin probe. (I) Summary of Delta2Tr mRNA injection experiments. GFP mRNA (1000 pg) was injected as a control. (J,K) The injected and uninjected sides, respectively, of an embryo injected with GR-Su(H)DBM mRNA (1000 pg) and induced with Dex. Arrows in J-O indicate endogenous FoxE3 expression in the PLE. (L) The injected side of an embryo injected with GR-Su(H)DBM but not induced with Dex. (M,N) The injected and uninjected sides, respectively, of an embryo injected with GR-Su(H)VP16 mRNA (1000 pg) and induced with Dex. Black and white arrowheads in M indicate ectopic FoxE3 expression in the ectoderm overlying the anterior brain and that surrounding the cement gland, respectively. (O) The injected side of an embryo injected with GR-Su(H)VP16 but not induced with Dex. |
