Talk:Evolution of nervous systems

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Wiki Education Foundation-supported course assignment[edit]

This article was the subject of a Wiki Education Foundation-supported course assignment, between 15 January 2019 and 25 April 2019. Further details are available on the course page. Student editor(s): Dback1219, Epoykhman. Peer reviewers: Vivianphann, Dvernet.

Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 20:58, 17 January 2022 (UTC)[reply]

Wiki Education Foundation-supported course assignment[edit]

This article was the subject of a Wiki Education Foundation-supported course assignment, between 20 January 2021 and 4 May 2021. Further details are available on the course page. Student editor(s): Adam.PerrettGCSU.

Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 20:58, 17 January 2022 (UTC)[reply]

Images[edit]

Don't currently have the insight to say if these are outdated but I've uploaded these images which may be relevant (on the other hand there are 1918 images in the article): <gallery> Image:Lawrence 1960 1.1.png|Evolution of the neuron Image:Lawrence 1960 1.1.svg|SVG (no labels): Evolution of the neuron Image:Lawrence 1960 1.2.png|Evolution of the central nervous system <gallery>

-- Kassyapias (talk) 13:36, 24 January 2017 (UTC)[reply]

Doubt about nervous system evolution[edit]

I think c. elagans is not the first one to study about nervous system. Please help me with this. Kassyapias (talk) 13:36, 24 January 2017 (UTC)[reply]

A Commons file used on this page has been nominated for deletion[edit]

The following Wikimedia Commons file used on this page has been nominated for deletion:

Participate in the deletion discussion at the nomination page. —Community Tech bot (talk) 21:07, 2 September 2018 (UTC)[reply]

Removed unsourced sections[edit]

I removed sections on neural induction and homeobox that were unsourced and have no direct relevance to the evolution of nervous systems. The content might be of use to develop other articles and so is copied below:

Removed content

Invertebrate Neural Induction[edit]

Neural induction represents the initial step in the generation of the nervous system and begins with the segregation of neural and glial cells from other types of tissues. Experiments and research pertaining to neural induction are focused on invertebrates, specifically C. Elegans and Drosophila as well as vertebrates, specifically frogs.

The neurogenic region of invertebrates begins at the ventrolateral regions of the embryo. In Drosophila Melanogaster, development begins once the ventral furrow folds into the embryo interior. The invaginated cells become the mesoderm, while the neurogenic region becomes more ventral. The closure of the furrow creates a midline that will become the site of neurogenesis. The neuroblasts of the ectoderm enlarge and squeeze away the epithelium layer through a process called delamination. Delamination occurs in 5 total waves, called niches, each creating about 60 neuroblasts. These neuroblasts undergo cell division to produce the "ganglion mother cell" (GMC). The GMC divides only once to produce neurons or glia.

Vertebrate Neural Induction[edit]

After fertilization, the egg is polarized into a vegetal hemisphere and an animal hemisphere. The animal hemisphere, at the top of the egg (the neurogenic region) has smaller cells than the rest of the egg. Following this polarization, a Blastula is formed after the egg undergoes multiple division, with a blactocoel being the outcome. The blastocoel differs from the blastula because of the tiny pocket or space that is created. Following this, the gastrula is formed via the process of gastrulation which leads to the creation of the neurula. Through this process, the neurogenic regions turns in to the neural plate, which in the precursor to the neural tube, which later becomes the brainstem.

The creation of the neural tube occurs once the neural plate folds inwards. Along with the neural tube, the neural crest is also created at this time, and it is the space in between the neural tube and the ectoderm. The neural crest produces the neurons and glia that lie outside of the central nervous system, such as the peripheral nervous system.

Molecular Signaling of Neural Induction[edit]

BMP signaling pathway
The Wnt signaling pathway

When discussing neural induction, there are several major pathways which ultimately regulate gene expression. Two signaling cascades which appear to effect gene expression early on are the BMP signaling pathway and the Wnt signaling pathway. The BMP pathway starts with BMPs binding to a receptor composed of type 1 and type 2 subunits. This receptor is a major determiner in setting up epidermal cells. When no BMP is present the removal of the animal cap leads to the creation of neurons. When BMP is present, the removal of the animal cap leads to epidermal cells. When the receptor is bound, the type 2 subunit phosphorylates the type 1 subunit. The phosphorylation of the type 1 subunit causes further phosphorylation of RSMAD protein. These phosphorylated RSMADs for a complex with coSMADs forming a RSMAD::coSMAD complex. This complex then moves into the nucleus. Once in the nucleus, the complex binds to DNA sequences called BMP response elements which are present in the promotor regions of genes. This initiates transcription.

Wnt and Shh pathway interaction

The Wnt process begins when the Wnt protein binds to a receptor called Frizzled. When Wnt is bound to the receptor, a second protein called β-catenin binds with several other proteins. Another protein called Disheveled prevents degradation of the formed complex only when Wnt is bound to Frizzled. As β-catenin accumulates, some of it moves into the nucleus where it complexes with TCF. The newly formed TCF β-catenin complex binds to DNA and activates transcription.

In frogs, involuting mesodermal cells of the involuting marginal zone release Chordin, Noggin, and Follistatin to inhibit BMP, causing the induction of neural tissue

Nervous system development is quite similar among thousands of different species, demonstrating an evolutionary connection of some kind. One of the primary examples of this is orthologs. Orthologs are any two or more homologous gene sequences found in different species that are related by linear descent. As stated previously, BMP inhibits neural differentiation in vertebrates. Drosophila Melanogaster possesses a molecule known as dpp, which also inhibits neural differentiation in a similar way. Sonic hedgehog (shh) is the morphogen of vertebrates that induces neural crest development by inhibiting BMP. Drosophila has sog, which inhibits dpp, causing similar results.

Homeobox (HOX) Genes in Invertebrates[edit]

After the formation of the regionally specified anterior-posterior axis, genes must be turned "on" to form unique structures in specific regions. This is orchestrated via the homeobox (Hox) transcription factor signaling pathway. First identified in Drosophila by Edward Lewis who won a Nobel Prize for the discovery.

Homeobox genes are organized in Drosophila along two complexes [Antennapedia complex (ANT-C) and Bithorax Complex (BX-C)]. A total of 8 genes are organized in the cluster based upon anterior-posterior expression. Homeobox proteins are transcription factors composed of a highly conserved 60 amino acid protein sequence present in many organisms. Homeobox proteins bind to specific sequences of the DNA of genes to regulate their expression.

HOX clusters like the ones in Drosophila have been identified in vertebrates. Although there are more HOX genes in vertebrates, the position of the HOX genes in relation to its expression along the A-P axis is conserved among species.

Hox genes in Drosophila
Rhombomeres in Humans

Homeobox Genes in Vertebrates (Rhombomeres)[edit]

Most experiments into the role of HOX genes in vertebrate nervous system development has come from studies about hindbrain formation. The hindbrain forms a segmented pattern reminiscent of the segments within the Drosophila embryo. In vertebrates, these segments of the hindbrain are referred to as rhombomeres.

The rhombomeres are numbered from the anterior most unit, r1, which is just posterior to the midbrain, to the posterior most unit, r8, at the border between the hindbrain and the spinal cord. Each rhombomere gives rise to a unique set of motor neurons that controls different muscles in the head. For example, r2 and r3 make the trigeminal motor neurons that innervate the jaw.

Example: The facial nerve motor neurons are mainly produced in r4 and the abducens motor neurons are produced in r5. Loss of the Hoxa1 gene in mice results in a complete loss of r5 and a reduction in r4. This causes severe shrinking of the facial nerve and a total loss of the abducens nerve.

Fences&Windows 16:12, 4 August 2019 (UTC)[reply]

The sections were added as part of Wikipedia:Wiki Ed/The George Washington University/Evolution of the Human Brain (Spring 2019). I would have hoped for better supervision and reviewing of these edits, Chetsherwood and Ian (Wiki Ed). Dback1219 and Epoykhman, I'm sorry tk have to undo your work, but in future you need to cite reliable sources and ensure the content is relevant, see WP:IRRELEVANT and the links in Template:Relevance and scope. Fences&Windows 16:33, 4 August 2019 (UTC)[reply]