Zebrafish (Danio rerio) are an important model organism that is particularly valuable for research in developmental biology. Zebrafish are extremely f…
Zebrafish are a small but powerful model system. These prolific fish can generate hundreds of offspring per week and many thousands over their lifetimes. Rapid external development and transparent bodies make the embryos ideal for diverse applications. This video will cover the basics of embryo collection and handling before describing current research methods that take advantage of zebrafish embryos.
In order to generate embryos, it helps to know a little bit about zebrafish mating behavior.
Zebrafish undergo sexual reproduction, so breeding requires both male and female fish. Males have slimmer bodies with a slightly red hue, while females have bigger, silver bellies full of eggs.
Periodic mating keeps eggs healthy, but making all those eggs takes a lot of work, so individual females should only be mated once per week.
Finally, like many other animals, sensory processes guide mating behavior in fish.
Olfactory cues from the male help to get his lady friend ready to spawn, while a little bit of mood lighting sets them both in action.
Having learned how to identify male and female fish, it’s time to set up a cross.
For zebrafish breeding, researchers use tanks specifically designed for mating. Breeding tanks typically feature a removable insert with holes that allow eggs to fall through. This feature protects the eggs from being eaten by hungry adult fish.
To begin, combine adult fish in breeding tanks during the afternoon or evening. To collect early stage embryos the following morning, separate male and female fish with a divider, which stops them from breeding before you’re ready to begin an experiment. To prevent the fish from jumping out, be sure to cover the breeding tank with a lid. Then, leave the fish to acclimate to each other overnight.
After spending the night together in a breeding tank, the fish will mate the following morning.
The first step in the morning is to remove the divider from between the male and female fish to initiate spawning. If a divider is not used, the fish will lay eggs shortly after light onset.
As the males chase the females around the tank, they stimulate spawning of eggs while releasing sperm into the water for fertilization. Wait approximately 15 - 30 minutes after pulling a divider to give the fish time to mate. Then, remove the adults from the tank by using a net or by lifting the tank insert and placing the fish into another tank.
Next, pour the water and the embryos through a mesh tea strainer for collection. Then, using “egg water,” wash the embryos off the strainer into a petri dish. It may be necessary to transfer embryos between dishes to achieve an optimal density of 50 - 100 per dish. To ensure development proceeds at a normal pace, place the dishes in an incubator at 28.5 °C.
Once you’ve got your embryos, handle them with care. They are important for your experiments! Let’s go over some pointers.
To keep embryos healthy, make sure to keep the water in the petri dishes clean and free of debris. Dead embryos will be opaque and should be removed daily. Additionally, methylene blue can be added to the water to prevent fungal growth.
Any time you need to move embryos from one dish to another, use a transfer pipet. By swirling the dish, you can concentrate the embryos in the center of the plate, making the pipetting easier.
Some protocols require a few additional steps for embryo maintenance. For the first three days of life, zebrafish embryos develop inside of a chorion, which can impede manipulation of the embryo. The chorion can be removed by treatment with the proteolytic enzyme, pronase, or by using forceps to remove it manually. Additionally, zebrafish begin to develop pigment by 24 hours, as shown here in this zebrafish larva, which can interfere with microscopy. To see through this problem, scientists supplement the embryo water with PTU, which inhibits production of the pigment melanin.
Now that you know how to obtain and care for zebrafish embryos, let’s explore some of the ways researchers use them for scientific discovery.
The external development of zebrafish embryos allows for genetic manipulation by microinjection of DNA, RNA, or gene knockdown reagents. This method leads to uniform distribution of injected material throughout the embryo and can produce visible phenotypes resulting from the overexpression or loss of a protein. The same technique can also be used to make transgenic fish in which specific structures are marked by the expression of fluorescent proteins.
Additionally, the small size of zebrafish embryos and larvae make them ideal for phenotypic chemical screening. Here, embryos are loaded into 96-well plates and then treated with libraries of small molecules by adding the chemicals into the water. Later, these plates of fish are screened for morphological defects, such as the abnormal development shown here.
Finally, the transparency of the zebrafish embryos makes them well suited for microscopy. Live embryos expressing fluorescent proteins in specific cell types can be mounted and visualized with confocal microscopy, allowing researchers to examine cell movements in developing tissues over time.
You’ve just watched JoVE’s video on zebrafish breeding and embryo handling. In this video, we’ve discussed the basics of mating, setting up breeding tanks, and embryo handling. We also discussed some research methods that take advantage of this powerful little embryo. Thanks for watching!
Zebrafish are a small but powerful model system. These prolific fish can generate hundreds of offspring per week and many thousands over their lifetimes. Rapid external development and transparent bodies make the embryos ideal for diverse applications. This video will cover the basics of embryo collection and handling before describing current research methods that take advantage of zebrafish embryos.
In order to generate embryos, it helps to know a little bit about zebrafish mating behavior.
Zebrafish undergo sexual reproduction, so breeding requires both male and female fish. Males have slimmer bodies with a slightly red hue, while females have bigger, silver bellies full of eggs.
Periodic mating keeps eggs healthy, but making all those eggs takes a lot of work, so individual females should only be mated once per week.
Finally, like many other animals, sensory processes guide mating behavior in fish.
Olfactory cues from the male help to get his lady friend ready to spawn, while a little bit of mood lighting sets them both in action.
Having learned how to identify male and female fish, it’s time to set up a cross.
For zebrafish breeding, researchers use tanks specifically designed for mating. Breeding tanks typically feature a removable insert with holes that allow eggs to fall through. This feature protects the eggs from being eaten by hungry adult fish.
To begin, combine adult fish in breeding tanks during the afternoon or evening. To collect early stage embryos the following morning, separate male and female fish with a divider, which stops them from breeding before you’re ready to begin an experiment. To prevent the fish from jumping out, be sure to cover the breeding tank with a lid. Then, leave the fish to acclimate to each other overnight.
After spending the night together in a breeding tank, the fish will mate the following morning.
The first step in the morning is to remove the divider from between the male and female fish to initiate spawning. If a divider is not used, the fish will lay eggs shortly after light onset.
As the males chase the females around the tank, they stimulate spawning of eggs while releasing sperm into the water for fertilization. Wait approximately 15 - 30 minutes after pulling a divider to give the fish time to mate. Then, remove the adults from the tank by using a net or by lifting the tank insert and placing the fish into another tank.
Next, pour the water and the embryos through a mesh tea strainer for collection. Then, using “egg water,” wash the embryos off the strainer into a petri dish. It may be necessary to transfer embryos between dishes to achieve an optimal density of 50 - 100 per dish. To ensure development proceeds at a normal pace, place the dishes in an incubator at 28.5 °C.
Once you’ve got your embryos, handle them with care. They are important for your experiments! Let’s go over some pointers.
To keep embryos healthy, make sure to keep the water in the petri dishes clean and free of debris. Dead embryos will be opaque and should be removed daily. Additionally, methylene blue can be added to the water to prevent fungal growth.
Any time you need to move embryos from one dish to another, use a transfer pipet. By swirling the dish, you can concentrate the embryos in the center of the plate, making the pipetting easier.
Some protocols require a few additional steps for embryo maintenance. For the first three days of life, zebrafish embryos develop inside of a chorion, which can impede manipulation of the embryo. The chorion can be removed by treatment with the proteolytic enzyme, pronase, or by using forceps to remove it manually. Additionally, zebrafish begin to develop pigment by 24 hours, as shown here in this zebrafish larva, which can interfere with microscopy. To see through this problem, scientists supplement the embryo water with PTU, which inhibits production of the pigment melanin.
Now that you know how to obtain and care for zebrafish embryos, let’s explore some of the ways researchers use them for scientific discovery.
The external development of zebrafish embryos allows for genetic manipulation by microinjection of DNA, RNA, or gene knockdown reagents. This method leads to uniform distribution of injected material throughout the embryo and can produce visible phenotypes resulting from the overexpression or loss of a protein. The same technique can also be used to make transgenic fish in which specific structures are marked by the expression of fluorescent proteins.
Additionally, the small size of zebrafish embryos and larvae make them ideal for phenotypic chemical screening. Here, embryos are loaded into 96-well plates and then treated with libraries of small molecules by adding the chemicals into the water. Later, these plates of fish are screened for morphological defects, such as the abnormal development shown here.
Finally, the transparency of the zebrafish embryos makes them well suited for microscopy. Live embryos expressing fluorescent proteins in specific cell types can be mounted and visualized with confocal microscopy, allowing researchers to examine cell movements in developing tissues over time.
You’ve just watched JoVE’s video on zebrafish breeding and embryo handling. In this video, we’ve discussed the basics of mating, setting up breeding tanks, and embryo handling. We also discussed some research methods that take advantage of this powerful little embryo. Thanks for watching!
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Q1: How do you identify male and female zebrafish for breeding?
Male zebrafish have slimmer bodies with a slightly red hue, while females have bigger, silver bellies full of eggs. Recognizing these physical differences is essential for setting up successful breeding crosses. Periodic mating keeps eggs healthy, but individual females should only be mated once per week to ensure their wellbeing.
Q2: What is the purpose of a removable insert in zebrafish breeding tanks?
Breeding tanks feature a removable insert with holes that allow eggs to fall through, protecting embryos from being eaten by adult fish. This design is critical for successful embryo collection. The insert can be lifted to remove adults after spawning, making the entire breeding process more efficient and reliable.
Q3: How long should you wait after removing the divider before collecting zebrafish embryos?
Wait approximately 15 to 30 minutes after pulling the divider to give the fish time to mate and spawn. During this period, males chase females around the tank, stimulating spawning while releasing sperm for fertilization. After this time, remove the adults and collect embryos by pouring water and embryos through a mesh tea strainer.
Q4: What is PTU and why is it used in zebrafish embryo culture?
PTU is a chemical that inhibits production of the pigment melanin in zebrafish embryos. Zebrafish begin developing pigment by 24 hours, which can interfere with microscopy observations. By supplementing embryo water with PTU, researchers can maintain transparency and improve visualization of developmental processes during live imaging studies.
Q5: What is dechorionation and when is it necessary for zebrafish embryos?
Dechorionation is the removal of the chorion, a shell-like membrane surrounding the embryo that can impede manipulation. For the first three days of life, zebrafish embryos develop inside this protective chorion. The chorion can be removed using the proteolytic enzyme pronase or manually with forceps, depending on experimental requirements.
Q6: How can zebrafish embryos be used for genetic manipulation in research?
The external development and transparency of zebrafish embryos allow for genetic manipulation through introduction microinjection early zebrafish embryos of DNA, RNA, or gene knockdown reagents. This method produces uniform distribution of injected material and can generate visible phenotypes from protein overexpression or loss. Transgenic fish with fluorescent protein markers can also be created for cell-type-specific visualization.
Q7: What daily care practices keep zebrafish embryos healthy in the laboratory?
Keep water in petri dishes clean and free of debris, and remove dead opaque embryos daily. Methylene blue can be added to prevent fungal growth. Maintain optimal embryo density at 50 to 100 per dish, and place dishes in an incubator at 28.5 degrees Celsius. Use a transfer pipet to move embryos between dishes, swirling the dish first to concentrate them in the center.