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Course: Biology library > Unit 22
Lesson 2: Signaling & transcription factors in developmentFrog development examples
How do you build a frog from a single cell? Learn how body axes are established and nerve tissue is induced in frog embryos.
Key points
- The African clawed frog, Xenopus laevis, is a popular model organism studied by many developmental biologists.
- The egg cell of a Xenopus frog is prepatterned by the mother frog with m
- Body axes begin to form when the sperm enters the egg, setting up the dorsal-ventral—back-belly—axis and a region called the gray crescent.
- The gray crescent turns into Spemann's organizer, a signaling center that "talks" with other tissues to direct development. Transplantation of an extra organizer into a newt embryo results in two newts joined at the belly!
- Signaling by Spemann's organizer is a classic example of induction, a process through which one tissue sends signals to change the development of another.
Introduction
When you were younger, did you ever grow frogs in an aquarium? I have vivid memories of watching tadpoles hatch and metamorphose into adults, a process I found simultaneously kind of gross and totally amazing.
Actually, I still feel that combo of reactions about a lot of developmental biology—whether frogs are involved or not! In development, many experiments involve dissecting, injecting, analyzing, or otherwise manipulating very tiny bits of developing tissue with results that are sometimes pretty bizarre—like a two-headed newt or a frog that develops as a blob of mystery cells.
However, these experiments are the only way we can discover the intricate networks of genes that program the development of living things. In a series of cascading, largely self-organizing events, these networks coordinate and carry out the development of a complex organism from a single cell. From a more practical standpoint, development is often closely linked to disease—for instance, human cancer cells turn many early developmental genes back on.
As mentioned in the intro to development article, the embryonic development of just about any organism involves processes like cell division, establishment of axes—such as the head-to-tail axis—tissue and organ formation, and cell differentiation. In this article, we'll see examples of these processes in frogs, though probably not the kind of frogs you'd have grown in a tank as a kid!
Xenopus: our friend the African clawed frog
To make the processes of development a little more concrete, let’s consider an example: our friend the frog. To be more exact, let’s use a frog that’s a favorite of developmental biologists: Xenopus laevis, or the African clawed frog. This bizarre-looking name is pronounced ZEN-oh-puss LAY-vis.
Xenopus has a relatively typical life cycle for a frog. A female frog lays eggs in the water, which are fertilized by sperm from a male frog. The resulting zygote goes through embryonic development to become a free-living tadpole, which then metamorphoses into an adult frog—for instance, by losing its tail through programmed cell death, or apoptosis.
Since Xenopus embryos develop outside of the mother frog's body, their development is much easier to watch than, say, the embryonic development of a mammal.
Let's look at a few selected parts of Xenopus embryo development to see how they illustrate some of the basic processes of development.
Cell division and axis formation
In frogs, the egg cell is a massive cell—much larger than a normal frog cell—and it has an uneven distribution of various molecules, which are deposited in the egg by the mother frog before fertilization.
The key cue that kicks off embryonic development is the entry of the sperm into the egg, which can occur anywhere on the dark-colored upper portion, or animal pole.
How does this work? When the sperm enters the egg, the cytoplasm at the edge of the egg cell, called the cortical cytoplasm, rotates 30 degrees towards the site of sperm entry.
The gray crescent corresponds to the future dorsal, or back, side of the embryo, while the the sperm entry site corresponds to the ventral, or belly, side.
What does the rotation of the cytoplasm actually do to establish this axis? The basic idea is that molecules specifying dorsal, or back, fate—which are initially located in the cortical cytoplasm of the yolky bottom part of the egg—get shifted upwards, towards the animal pole of the zygote.
At this point, we're still looking at one big zygote. So, where do these cells we're talking about come from? An early Xenopus embryo is pretty much a cell division machine. Through many repeated rounds of cell division, the zygote—with its unequally distributed m
Making tissues and organs
How does our friend the frog go from a ball of cells to something that looks more like, well, a frog? The tadpole that forms in embryogenesis is the result of a huge number of genes being expressed in specific patterns and of their protein products interacting in different ways to set up yet other patterns of gene expression. A frog embryo is an amazing, self-organizing system, in which one molecular event triggers another in a cascade in time and space.
Understanding all of those events would be the work of a lifetime—so we're not going to attempt it in this article! In fact, even the best developmental biologists are pretty far away from understanding how a frog develops in full, Technicolor molecular detail. However, we can see one classic example of cascading events in development by looking at the behavior of cells in a particular area of the embryo—the area that develops from the gray crescent.
Case study: Spemann-Mangold organizer
What happens to the gray crescent we saw in the zygote? Let's trace where the cytoplasm from this area ends up in two later stages: blastula and gastrula.
The blastula is a ball of cells with a hollow space in the middle. In it, the gray crescent cells are found in a group on one side of the embryo, the dorsal side. This is pretty much where the gray crescent was in the zygote.
At the gastrula stage, however, these cells do something more interesting: they start marching into the interior of the embryo, causing the tissue to fold inward. The site where the cells migrate into the interior of the embryo is called the blastopore, and the gray crescent cells make up its dorsal lip.
What is the purpose of all this complex cell migration? For one thing, it's key to forming multiple layers of tissue in the embryo. But it's not just a matter of creating more layers; it's also a matter of cells in different tissues "talking" with one another and, in some cases, changing each other's fate. For instance, we now know that the cells that migrate inward instruct the cells above them, a type of tissue called ectoderm, to develop into neural—nervous system—tissue.
This interaction was first discovered in the 1920s by Hans Spemann and Hilde Mangold, in what is now one of the most classic experiments in embryology. Spemann and Mangold took the dorsal blastopore lip from a light-colored newt embryo and transplanted it into the belly, or ventral, side of a dark-colored newt embryo. This was a very technically demanding experiment, and Mangold worked for years to get five embryos in which it worked correctly!
Normally, the tissue at the transplant site would have turned into skin on the newt's belly, the ventral side. However, when the chunk of dorsal blastopore lip was transplanted in, its cells migrated inward, creating a second, functional gastrulation site opposite to the normal one.
What exactly happened in this experiment? There were two basic possibilities for how the transplanted tissue could have led to the formation of the second newt:
- The transplanted tissue might have developed into the second newt all by itself, building its structures from the small group of transplanted cells.
- The transplanted tissue might have "talked" to the layers of recipient tissue around it, organizing their behavior so that they—along with the transplanted cells—coordinated to form a second newt.
Thanks to the use of different-colored newts as donor and recipient, Mangold and Spemann were able to tell which possibility was correct. The structures found in the second newt's body consisted of some donor—light—cells but mostly recipient—dark—cells, meaning that cells in the transplanted tissue must have “talked” with the recipient cells nearby and induced them to change their behavior.
Today, the cells of the dorsal blastopore lip and their descendants are called the Spemann-Mangold organizer. Two of the organizer's key roles are to specify dorsal—back, rather than belly—fate and to make nearby ectoderm turn into neural tissue. However, the organizer also guides head-tail axis development and other processes.
Importantly, the organizer itself doesn't directly guide the development of the entire newt. That is, it doesn't pull the strings, so to speak, that make each neuron in the newt's brain or photoreceptor in the newt's eye develop. Instead, it starts a chain reaction of molecular induction events that lead, domino-like, to the formation of the many complex structures of the newt's body—or, in the case of a transplant, to a second newt body!
The organizer acts largely by releasing secreted proteins that diffuse into the surrounding tissues and affect their behavior. For instance, some of the proteins released by the organizer bind to and neutralize other secreted proteins, which instruct cells to develop as skin. By interfering with the “Develop as skin!” cues, the organizer signals allow the overlying tissue to develop as neural tissue, actually its default path.
Want to join the conversation?
Which part is the archenteron or coelom?(5 votes)
This response is a few years late, but for those wondering... In late gastrula of figure. 6?, the archenteron is the space that forms from the blastopore lip. In blastula, you can see the blastocoel as the cavity at the top, it disappears shortly after the archenteron is formed.(5 votes)
How is the uneven distribution of the molecules in the egg kept like that? Wouldn't the molecules tend to spread out evenly, even if they were positioned on one side of the cell in the beginning?(3 votes)- What I recall, in fruit flies, all the chemicals are locked on one side of the egg, and unlocked/released by molecules provided by sperm at time of fertilization. Once unlocked, the chemicals diffuse producing a gradient. Overtime, the chemicals will be uniformly distributed like you mentioned, and no longer be useful as location marker.(4 votes)
"In fact, I remember one of my professors telling us that you could squeeze a female Xenopus frog "like a tube of toothpaste" to get the eggs out for experiments!"
Wouldn't that hurt the frog? Or do scientists not care about that if they need something for their experiments? I'm sorry about how blunt this sounds, but I am vegan and a strong believer in animal rights, and was just wondering if some scientists use more humane methods to get what they need for their research.(2 votes)- I agree and am curious as well, as to the humaneness of the methods used. I believe that all living beings should be treated the most humane way possible. Are there ethics guidelines regarding the use of animals in research? What do these guidelines entail?(3 votes)
is there a part where I can disect a frog(2 votes)
did this experiment have to be with light and dark embryos, or could it be that the only reason Hans Spemann and Hilde Mangold did that was to check at the end of the experiment if those cells really did use induction?(2 votes)- Which organ is developed first in the frog embryo?(2 votes)