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Determining Orientation in the Development of the Neural Tube

Jim Hutchins

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The role of Hedgehog signaling

Fig. 7.—Diagrams to show the formation of the neural tube, notochord, mesoderm, and coelom in vertebrates, based on Amphibia. Cross-sections. A, differentiation of the notochord f in the roof of the entoderm (endoderm); mesodermal plates b spreading ventrally. B, neural folds h rising at the sides of the medullary plate g; notochord f separated from the entoderm; mesodermal plates b extended farther ventrally and developing a central cavity, the coelom i. C, neural folds h nearly closed to form the neural tube j; mesodermal plates have reached the midventral line; coelomic split i has extended ventrally. a, ectoderm; b, mesoderm; c, entoderm or archenteron; d, somatic mesoderm; e, splanchnic mesoderm; f, notochord; g, medullary plate; h, neural fold; i, coelom; j, neural tube. (A from Hertwig-Mark’s Textbook of the Embryology of Man and Mammals, courtesy of the Macmillan Company.)

Diagram showing the gradient of Sonic Hedgehog concentration in the notochord and neural tube.Figure 4. Formation and patterning of the mouse neural tube. (A) The pseudostratified columnar epithelium of neural plate forms by 7.5 dpc. The lateral edges of the neural plate then (B) elevate and (C) fold by ~8.0 dpc before (D) converging at the midline and closing by ~8.5 dpc. Shh (red arrows) and BMP inhibitors secreted from the floor plate, and BMP4/7 (green arrows) secreted from the roof plate act to pattern the neural tube along its ventro-dorsal axis, giving rise to the layers of the spinal cord (Gilbert, 2006). Key: V, ventral; D, dorsal; L, left; R, right.

Protein structure of Sonic Hedgehog.
Mouse sonic hedgehog complex with sulfate (sulfur atom obscured by four red oxygen atoms) and Zn2+ ion (grey) (PDB code 1vhh)

 

Diagram showing the steps of Sonic Hedgehog signaling. Step 1: unbound Patched holds Smoothened in an intracellular vesicle membrane.In the absence of a Shh signal, a 12 transmembrane receptor protein called Patched blocks the function of Smoothened (Smo), a seven-pass transmembrane protein, by keeping it sequestered in an intracellular vesicle (Figure 3)[16]. When Shh binds to Patched, inhibition of Smo by Patched is relieved. Patched becomes endocytosed, and Smo translocates to the cell surface. In vertebrates, Smo localizes to the surface of the primary cilium, initiating a signaling cascade that leads to the activation of Gli transcription factors [8]. Present in both the nucleus and cytoplasm, there are three of these regulatory proteins (Gli1, Gli2, and Gli3). Following Shh signaling, all three proteins can act as transcriptional activators of Shh target genes. Gli3, however, can act as both an activator and repressor; in the absence of Shh signaling, Gli3 is cleaved by the proteasome, and its truncated form accumulates in the nucleus where it represses transcription of Shh-responsive genes (Figure 3) [16].

https://proteopedia.org/wiki/index.php/Sonic_Hedgehog

Randi Woodbeck, Michal Harel, Joel L. Sussman, David Canner, Riley Hicks, Andrea Gorrell, Alexander Berchansky

Diagram showing the steps of Sonic Hedgehog signaling. Step 2: Smoothened and Patched switch places.Diagram showing the steps of Sonic Hedgehog signaling. Step 3: The G protein Smoothened releases an inhibitory alpha subunit which inhibits adenylate cyclase and reduces cAMP levels.

Diagram showing the steps of Sonic Hedgehog signaling. Step 4: reduced cAMP levels result in the transcription factor Gli1 activating the genes involved in being a ventral neural tube cell.

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Developing Expertise in Neuroscience Copyright © 2024 by Jim Hutchins is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License, except where otherwise noted.