XB-IMG-49517
Xenbase Image ID: 49517
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Figure 6. Quadruple Knockdown of BMP2/4/7 and ADMP Results in Ubiquitous CNS Formation In Vivo
(A) CNS marked by Sox2 in control embryos; inset shows frontal view (DAI = 5.2).
(B) Knockdown of ADMP moderately increases Sox2 expression in anterior CNS (inset) (DAI = 6.2).
(C) Triple knockdown of BMP2/4/7 results in embryos with a neural plate approximately 5 times the width of that of control siblings (transversal section
shown in inset).
(D) Quadruple inactivation of BMP2/4/7 and ADMP (9 ng total each) results in radially dorsalized embryos and ubiquitous neural differentiation in the ectoderm
(DAI = 9.7; n = 59).
(E) Cytokeratin expression marks epidermal cells on the surface of control embryos.
(F) Expression of epidermal Cytokeratin is abolished in Bmp2/4/7/Admp morphants at stage 16.
(G and H) BMP2/4/7/ADMP-deficient embryos express radial Otx2, Rx2a, and Krox20.
(I) Quadruple Chordin/Noggin/Follistatin/Cerberus MO-injected embryos are strongly ventralized (DAI = 2.3) but retain posterior CNS (compare to [K]).
(J) ADMP is held inactive by forming a stable inhibitory ternary complex with Chordin and Tsg. DN-Xlr inhibits Xolloid-related (Xlr), preventing the proteolytic
cleavage of Chordin at two specific sites.
(K) Sox2 in wild-type embryos.
(L) Injection of DN-Xlr mRNA (400 pg) broadens Sox2 expression.
(M) Simultaneous knockdown of BMP2/4/7/ADMP and of Chordin/Noggin/Follistatin/Cerberus display ubiquitous neural induction, indicating that BMP ligands
are epistatic to their secreted antagonists.
(N) Blastocoele injection (40 nl) of Noggin-Fc (0.5 mM) or Chordin (1 mM) protein causes complete neuralization of ectoderm.
(O) BMP2/4/7-depleted embryos retain nonneural ectoderm.
(P) Ubiquitous neural differentiation in BMP2/4/7-depleted embryos injected with DN-Xlr mRNA; this experiment suggests that Chordin cleavage by Xlr is
required for ADMP-mediated epidermal differentiation. Image published in: Reversade B and De Robertis EM (2005) Copyright © 2005. Image reproduced with permission of the Publisher, Elsevier B. V.
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