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Gastrulation is a phase of development where the three embryonic germ layers (endoderm, mesoderm, and ectoderm) are constructed through various mechanisms of morphogenic cell movement. This stage is initiated at the blastopore of the dorsal lip, which is formed on the opposite side of the embryo from where the sperm enters. The dorsal lip is part of the blastopore located below the Spemann's organizer that becomes elongated and eventually circularized. The blastopore is the point of access for the outer cells to enter the embryo. The cells around the blastopore undergo apical constriction and are referred to as bottle cells because of their shape. Invagination occurs at the blastopore. This is where cell sheets of the marginal zone fold inward in order to construct a pocket. This pocket develops into a fluid-filled cavity located in the middle of the embryo referred to as a blastocoel.

Multiple types of morphogenic cell movement is involved throughout gastrulation. These processes do not rely on one another; however, the overall result of their actions are what drives the differentiation of the germ layers. Epiboly, invagination, involution, and convergent extension are clearly seen in Xenopus gastrulation. Epiboly can be seen in the animal hemisphere. These cells flatten and spread out to increase the surface area of the cell sheet in order to cover the whole surface of the embryo. The outer cells move towards the blastopore of the dorsal lip causing the marginal zone to invaginate, creating a circular blastopore. During invagination, the blastocoel moves up towards the top of the animal pole, away from the dorsal lip, and subsequently down to the vegetal pole. While doing this, its size decreases due to the infiltrating cells. Eventually, the blastocoel shrinks and the archenteron, which is the early structure of the gut, becomes the principle cavity. Because the mesoderm is already located on the inside of the gastrula, involution allows it to separate into a whole different layer forming between the endoderm and the ectoderm. Involution is a process where a cell sheet folds inward, forming an underlying layer of cells (mesoderm).

Convergent extension is a process where cells line up based on their polarity and move between neighboring cells through the use of lamellapodia, generating shape change at the tissue level. Cellular intercalation occurs in all three germs layers which moves the marginal zone internally, further closing the blastocoel. Convergent extension is one of the more well-studied cellular movements involved in gastrulation. The Wnt/β-catenin pathway is necessary for convergent extension to occur. Proper execution of this pathway leads to dorsal cell specification. The Xnr-3 protein is a major target of this pathway and if it is not expressed correctly, then the cells do not undergo proper convergent extension. Paraxial protocadherin (PAPC) plays an important role in cell movement as well regarding planar cell polarity and the Wnt pathway. It is dependent on three GTP proteins RhoA, Rac1, and JNK.

The end of gastrulation results in a structure called a gastrula. The three embryonic germ layers are now differentiated in the embryo. The innermost layer is the endoderm that was originally the vegetal tissue. The outermost layer is the ectoderm, which was once the animal cap. The middle layer is the mesoderm that was formed from the involution of the marginal zone.

The next phase of development is neurulation where the neural tube is formed giving rise to the central nervous system. During this stage, the embryo is referred to as a neurula. Neurulation is initiated when ectodermal cells thicken, forming the neural plate. These cells change in shape from cuboidal to columnar, causing the edges of the plate, referred to as neural folds, to rise towards one another which is caused by the constriction of F-actin during apical constriction. As these boundaries move, the middle of the neural plate descends to form the neural groove. The neural tube forms when these two folds meet to form a hollow cylinder that becomes covered with a layer of the ectoderm known as the epidermis. Deep cells, which are non-neural cells, help bring the two folds together. The Wnt pathway also plays a critical role in these cell movements. Wnt needs to inhibit BMP in the gastrula stage and then BMP needs to be activated in the neurula for proper neural crest formation. Sox2 is shown to be consistently expressed throughout neurulation. There are hinge points located along the neural tube that aids in closing it. This happens almost simultaneously. Convergent extension is consistently being carried out, especially in the notochord, resulting in the elongation of the entire body.

Fig analysis cite for F-cadherin

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Introduction
Development is highly conserved process, which includes fertilization, cleavage, gastrulation, nuerulation, and axis formation. Each of these phases are required in order for a species to develop from a single egg cell, into a fully functioning multicellular adult. While this process is highly conserved, there are variations in the mechanisms used by species to undergo each phase. This article will focus on the overall development Xenopus laevis, and the mechanisms used by the African clawed frog during each phase of development.

Life Cycle
The life cycle of Xenopus laevis takes roughly twelve months from start to finish. That is, from fertilization to adulthood. It is important to note that the earliest stages of the frogs’ life cycle only take about 24 hours to complete, it is the unique process of metamorphosis that takes the longest. The first stage of the life cycle is fertilization.

Fertilization
Fertilization is the event that sets the entire process of development into motion. In Xenopus it occurs externally, meaning that the male frog disperses his sperm across the eggs in the environment. A single sperm enters the egg and triggers it to revolve so that the animal pole is in its proper position. Without this rotation the gray crescent would not be properly set up and the next step, which is cleavage, would not occur correctly.

Cleavage
Cleavage is the second step of development and is important because it establishes the different poles and makes sure that the organizers are being put in place. Cleavage is what its name implies, separations of the egg without growth of the cells.

CLEAVAGE:

Cleavage refers to a set of early cell divisions, these divisions occur without cellular growth and yield multiple smaller cells originating from one cell. Cleavage in Xenopus occurs in an orderly manner and the first cleavage splits the egg vertically down the middle, into anterior and posterior halves. The second cleavage occurs roughly perpendicular to the axis of the first and divides the egg into dorsal and ventral halves. Cleavage continues and around the 32 cell stage, the formation of the blastocoel is observed, the blastocoel is a cavity that forms in the Animal hemisphere. When the formation of the blastocoel is noted, the embryo is referred to as a blastula. Cells composing the blastula are joined by cadherins, which are calcium dependent adhesion's, and thus the removal of Ca2+ degrades the cadherins. Cleavage continues until the mid-blastula transition, this prompts for a decrease in cleavage divisions and promotes transcription of the zygotic genome.

Intracellular Ca2+ is essential for cleavage to occur in Xenopus laevis, Evidence indicates that cell cleavage involves narrowing of the region in which the cleavage furrow is located. The mechanism involved in the contraction of the area has been associated with that of muscle, and is thought to contain an actin-myosin based structure. This structure utilizes calcium, thus Ca2+ is required in order for cleavage to occur.

The formation of the organizer (Spemann's organizer) during the final cleavage divisions is a crucial step required for the remaining phases of development. The organizer is an area located in the posterior/dorsal area of the embryo, and is responsible for expression of many genes involved in axis formation. This area is crucial in gastrulation, as it forms the area known a the dorsal lip of the blastopore.

Gastrulation
Gastrulation is a phase of development where the three embryonic germ layers (endoderm, mesoderm, and ectoderm) are constructed through various mechanisms of morphogenic cell movement. This stage is initiated at the blastopore of the dorsal lip, which is formed on the opposite side of the embryo from where the sperm enters. The dorsal lip is part of the blastopore located below the Spemann's organizer that becomes elongated and eventually circularized. The blastopore is the point of access for the outer cells to enter the embryo. The cells around the blastopore undergo apical constriction and are referred to as bottle cells because of their shape. Invagination occurs at the blastopore. This is where cell sheets of the marginal zone fold inward in order to construct a pocket. This pocket develops into a fluid-filled cavity located in the middle of the embryo referred to as a blastocoel.

Multiple types of morphogenic cell movement is involved throughout gastrulation. These processes do not rely on one another; however, the overall result of their actions are what drives the differentiation of the germ layers. Epiboly, invagination, involution, and convergent extension are clearly seen in Xenopus gastrulation. Epiboly can be seen in the animal hemisphere. These cells flatten and spread out to increase the surface area of the cell sheet in order to cover the whole surface of the embryo. The outer cells move towards the blastopore of the dorsal lip causing the marginal zone to invaginate, creating a circular blastopore. During invagination, the blastocoel moves up towards the top of the animal pole, away from the dorsal lip, and subsequently down to the vegetal pole. While doing this, its size decreases due to the infiltrating cells. Eventually, the blastocoel shrinks and the archenteron, which is the early structure of the gut, becomes the principle cavity. Because the mesoderm is already located on the inside of the gastrula, involution allows it to separate into a whole different layer forming between the endoderm and the ectoderm. Involution is a process where a cell sheet folds inward, forming an underlying layer of cells (mesoderm).

Convergent extension is a process where cells line up based on their polarity and move between neighboring cells through the use of lamellapodia, generating shape change at the tissue level. Cellular intercalation occurs in all three germs layers which moves the marginal zone internally, further closing the blastocoel. Convergent extension is one of the more well-studied cellular movements involved in gastrulation. The Wnt/β-catenin pathway is necessary for convergent extension to occur. Proper execution of this pathway leads to dorsal cell specification. The Xnr-3 protein is a major target of this pathway and if it is not expressed correctly, then the cells do not undergo proper convergent extension. Paraxial protocadherin (PAPC) plays an important role in cell movement as well regarding planar cell polarity and the Wnt pathway. It is dependent on three GTP proteins RhoA, Rac1, and JNK.

The end of gastrulation results in a structure called a gastrula. The three embryonic germ layers are now differentiated in the embryo. The innermost layer is the endoderm that was originally the vegetal tissue. The outermost layer is the ectoderm, which was once the animal cap. The middle layer is the mesoderm that was formed from the involution of the marginal zone.

Gastrulation is the next step of development and is where the cells in the embryo are moved into their designated locations. The three germ layers are also set apart during this time and the organizer is set up on the dorsal side of the embryo, this is vital to neurulation.

Neurulation
The next phase of development is neurulation where the neural tube is formed giving rise to the central nervous system. During this stage, the embryo is referred to as a neurula. Neurulation is initiated when ectodermal cells thicken, forming the neural plate. These cells change in shape from cuboidal to columnar, causing the edges of the plate, referred to as neural folds, to rise towards one another which is caused by the constriction of F-actin during apical constriction. As these boundaries move, the middle of the neural plate descends to form the neural groove. The neural tube forms when these two folds meet to form a hollow cylinder that becomes covered with a layer of the ectoderm known as the epidermis. Deep cells, which are non-neural cells, help bring the two folds together. The Wnt pathway also plays a critical role in these cell movements. Wnt needs to inhibit BMP in the gastrula stage and then BMP needs to be activated in the neurula for proper neural crest formation. Sox2 is shown to be consistently expressed throughout neurulation. There are hinge points located along the neural tube that aids in closing it. This happens almost simultaneously. Convergent extension is consistently being carried out, especially in the notochord, resulting in the elongation of the entire body.

Neurulation follows gastrulation and utilizes the germ layers and organizer set up that occurred during that stage. The early form of the nervous system is set up during this time, it is called the neural plate.

Organogenesis
Organogenesis benefits from the earlier stages because it requires the organizer and nervous system. The three germ layers, which were established during gastrulation, now respond to signaling and set up the organ systems.

Research shows that there are cells that support the germ layers in forming the organs during this time. These cells come from the immune system assist in creating organs such as kidneys.

Metamorphosis
Metamorphosis is the last stage of the developmental process and is a defining moment for Xenopus. The defining characteristics of the tadpole, such as the tail and gills, shrink and are replaced by arms, legs, and useful lungs.

TR hormones have been found to play an active role in the changes that occur during metamorphosis. They are found in the head, middle, and tail regions of the changing tadpole both before and after the change.

Axis Formation
All axis formation is centered around the organizer, which is located on the dorsal side of the developing embryo. The organizer is set up in this location because of the Nieuwkoop center. Axis formation is important to the development of Xenopus because without it the frog would lack proper body formation and more than likely would not survive.

Dorsal/Ventral
The dorsal and ventral body axis are the product of mainly two organizers. The first is Wnt, which signals on the dorsal side of the embryo. The other organizer responsible for setting up this axis is BMP, which is found on the ventral side of the embryo.

Research has been done on the specific forms of Wnt within the embryo and during the setup of the axis. It has been found that Wnt11 work in conjunction with one another to establish the dorsal side of the embryo. It has also been found that Dkk1 assists the two forms of Wnt in influencing only where they are supposed to go. This is achieved by it repressing and initiating the function of Wnt.

Anterior/Poster
Wnt and BMP not only influence the development of the dorsal and ventral axis, they are also the key players in the establishing of the anterior posterior axis. BMP is credited with congregating in the anterior side of the embryo. Wnt, on the other hand is found in the posterior.

Left/Right
The final axis that is present in the developing embryo is the left and right axis. This axis is unique from the others because it is regulated primarily by rotating cilia, whereas the others are set up by repression/expression of organizers. Pitx2 is a left signaling organizer, and as mentioned, it is set up on the left side because of the rotating of the cilia. The cilia are in the node and as it receives the Pitx2 from the organizer is carries it over.

Research has been done on the importance of the placement of the cilia for the equal spreading of the organizer, and therefore the proper setup of the axis. The cilia traditionally develop on the posterior side of the embryo, and carry out their function from there. They receive the signals that they need to develop in this area from Vangl2. It was discovered that if the Vangl2 levels were not held at steady amounts, the cilia grew in a more central location. This completely upsets the spread of Pitx2 and therefore causes the left and right axis to form incorrectly, or not at all.