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Danio rerio

FAMILY

Cyprinidae

TAXONOMY

Cyprinus rerio Hamilton, 1822, Kosi River, Utter Pradesh, India.

OTHER COMMON NAMES

English: Zebra danio, striped danio; German: Zebrabärbling.

PHYSICAL CHARACTERISTICS

Small fish, rarely grows beyond 1.97–2.36 in (50–60 mm) in length. Body slender, slightly compressed. Two pairs of barbels: rostral barbels extend to anterior margin of orbit; maxillary barbels end at about middle of opercle. Dorsal fin with 3 unbranched, 7 branched rays. Anal fin striped, with 3 unbranched, 10–12 branched rays. Lateral line incomplete or absent. Vertebrae 31–32. Body silvery, sometimes tinted with

gold, with five blue horizontal stripes on the sides. Stripes also present in the anal and caudal fins.

DISTRIBUTION

Native to tributaries of the Ganges River, along the Coromandel Coast of India, from Calcutta to Masulipatam, Bengal, Nepal, Pakistan, and Bangladesh. As aquarium fish and experimental animal, it has been introduced worldwide.

HABITAT

Slow-moving and still water bodies such as streams, canals, ditches, and ponds, particularly rice fields.

BEHAVIOR

Very active, usually swimming in schools.

FEEDING ECOLOGY AND DIET

Feeds mainly on worms and small crustaceans. It also feeds on insect larvae and can be used for mosquito control.

REPRODUCTIVE BIOLOGY

Matures in 4–6 months. Females are larger and have less vibrant coloration than males. Typically, spawning occurs in the early hours of the morning. Eggs are semiadhesive, relatively large, and released into open waters. Under experimental conditions, this species spawns at intervals of 1.9 to 2.7 days. However, spawning intervals in nature are typically much longer, varying from 5 days to several weeks. Between 21 and 60 eggs are released per spawning event. In captivity, the total number of eggs spawned is usually between 400 and 500. Eggs hatch approximately 20–48 hours after spawning. Larvae live from 48 to 72 hours on their yolk-sac provision.

CONSERVATION STATUS

Not listed by IUCN.

SIGNIFICANCE TO HUMANS

Because of their small size, zebrafish are of no value as a food fish. However, they are very popular aquarium fish and also very important as experimental subjects for genomic study.

 
 

The zebrafish (Brachydanio rerio) is a small tropical freshwater fish that began to be used as a genetic model system in the early 1980s. The zebrafish shares numerous anatomical and genetic similarities with higher vertebrates, including humans, both in the general body plan and in specific organs. Close parallels exist in many aspects of early embryogenesis and in the anatomical and histological features of the brain, spinal cord, sensory systems, cardiovascular system, and other organs. Not infrequently, genetic defects in zebrafish resemble human disorders. Owing to these similarities, zebrafish genetics is being broadly applied to address both basic biological questions and to model human inherited diseases.

Useful Traits for Researchers

Several characteristics favor the choice of zebrafish for genetic research. First, zebrafish are easy to maintain in large numbers in a small laboratory space. Second, their generation time is relatively short: three months. Finally, females produce large clutches of offspring, about 50 to 100 a week. The zebrafish also presents advantages for embryological analysis: Its embryos develop externally, and are largely transparent for the first 36 hours of development.

The first proponents of the zebrafish model, George Streisinger and his colleagues at the University of Oregon, outlined its genetic characteristics and provided a thorough description of zebrafish embryogenesis. Zebrafish research entered a new phase when two groups, at the University of Tuebingen (Germany), and at Harvard Medical School, performed large-scale chemical mutagenesis experiments and isolated nearly 2,000 mutations that affect almost every aspect of embryonic development, from gastrulation to axonal pathfinding. Once the mutations were identified, they were studied to determine their developmental effects, after which their genetic and molecular nature was analyzed. These early genetic studies in zebrafish were limited by the lack of genomic resources, such as maps of the genome or genomic libraries, but these deficiencies were gradually eliminated during the late 1990s. Zebrafish research has entered a new phase since the completion of the genome project. This effort provided the sequence of the entire zebrafish genome and made cloning of zebrafish genes much more efficient.

Ongoing Research Involving Zebrafish

Zebrafish research continues at a fast pace. New rounds of mutation identification are in progress. To supplement chemical mutagenesis, retroviral vectors were developed as mutagenic agents and applied on a large scale. Tools to study the functions of individual genes, such as transgenics, were developed in parallel to mutant screening approaches. A technique that complements mutagenesis screens in zebrafish very well is known as gene knockdown. This approach uses modified antisense oligonucleotides to block the function of specific genes. These oligonuculeotides contain a substitution of the sugar ring in the nucleic acid backbone that makes them resistant to degradation by enzymes in living tissues. Gene knockdown is widely used to study mutant phenotypes of genes for which chemically induced mutations are not available.

The usefulness of the zebrafish as a model organism originates in its unique combination of genetic and embryological characteristics. Genetic approaches, such as mutagenesis screens, can be combined in zebrafish with other techniques, enabling researchers to study cell movements, cell birth dates, or interactions between cells in the living embryo. Although most of the zebrafish genetic research focuses on embryonic development, other problems, such as the genetic basis of circadian rhythms, cancer formation, neurodegenerative disorders, and drug addiction, are also being addressed.

Bibliography

Amsterdam, A., and N. Hopkins. "Retrovirus Mediated Insertional Mutagenesis in Zebrafish." Methods of Cell Biology 60 (1999): 87-98.

Driever, W., et al. "A Genetic Screen for Mutations Affecting Embryogenesis in Zebrafish." Development 123 (1996): 37-46.

Haffter, P., et al. "The Identification of Genes with Unique and Essential Functions in the Development of the Zebrafish, Danio rerio." Development 123 (1996): 1-36.

Kimmel, C. B., et al. "Stages of Embryonic Development of the Zebrafish." Development Dynamics 203 (1995): 253-310.

Malicki, Jarema. "Harnessing the Power of Forward Genetics: Analysis of Neuronal Diversity and Patterning in the Zebrafish Retina." Trends in Neuroscience 23 (2000): 531-541.

Nasevicius, A., and S. C. Ekker. "Effective Targeted Gene 'Knockdown' in Zebrafish." Nature Genetics 26 (2000): 457.

Thisse, C., and L. Zon. "Organogenesis-Heart and Blood Formation from the Zebrafish Point of View." Science 295 (2002): 216-220.

Westerfield, M. The Zebrafish Book. Eugene: University of Oregon Press, 1994.

Internet Resource

Zebrafish Information Network. http://zfin.org.

—Jarema Malicki

 
Wikipedia: zebrafish
For the venomous Australian coral reef fish which is also known as zebrafish, see red lionfish.
Danio rerio
Zebrafisch.jpg
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
Order: Cypriniformes
Family: Cyprinidae
Genus: Danio
Species: D. rerio
Binomial name
Danio rerio
(Hamilton-Buchanan, 1822)
Synonyms
  • Barilius rerio
  • Cyprinus chapalio
  • Brachydanio rerio
  • Cyprinus rerio
  • Danio lineatus
  • Nuria rerio
  • Perilampus striatus

The zebrafish or zebra danio, Danio rerio, is a tropical fish belonging to the minnow family (Cyprinidae).[1] It is a popular aquarium fish, where it is frequently sold under the trade name zebra danio, and is also an important model organism.

Taxonomy

The zebrafish is a derived member of the genus Danio. It has a sister group relationship with Danio kyathit.[2]

Distribution

The zebrafish is native to the streams of South-eastern Himalayan region.[2] The zebrafish arose in the Ganges region in Eastern India and is also native to Pakistan, Bangladesh, Nepal and Myanmar. It commonly inhabits streams, canals, ditches, ponds and slow-moving to stagnant water bodies, including rice fields.

Zebrafish have been introduced in Japan and the United States as well as Australia, where they are kept in aquariums. [1]. They have also been sighted in Colombia, presumably having escaped from an aquarium.

Description

The fish is named for its five uniform, pigmented, horizontal blue stripes on the side of the body, all of which extend to the end of the caudal fin. Males are torpedo shaped and have gold stripes between the blue stripes; females have a larger, whitish belly and have silver stripes instead of gold. The zebrafish grows to 3.8 cm, lives for around 5 years, and produces 300-500 eggs per spawning.

Varieties

Recently, transgenic zebrafish have become commercially available that express green fluorescent protein, red fluorescent protein, and yellow fluorescent protein. These fish are tradenamed GloFish. Other varieties include leopard and longfin.

The Leopard danio, previously known as Danio frankeri, is a spotted colour morph of the zebrafish Danio rerio caused by a pigment mutation.[3] Xanthistic forms of both the zebra and leopard pattern, along with long-finned varieties have been obtained via selective breeding programs for the aquarium trade.[4]

Aquarium Care

Zebrafish are hardy fish and considered good for beginner aquarists. Their ease of keeping and breeding, beauty, price and broad availability may all contribute to their popularity. They thrive best at temperatures above 22 degrees celsius and below 27 degrees celsius. They also thrive as shoals of 6 or more, although they do interact well with other fish types in the Aquarium. However, they are susceptible to Oodinium, or Velvet disease, Microsporidia (Pseudoloma neurophilia),and mycobacterium species.

Model organism for development and genetics

Zebrafish chromatophores, shown here mediating background adaptation, are studied by scientists
Enlarge
Zebrafish chromatophores, shown here mediating background adaptation, are studied by scientists

D. rerio are a common and useful model organism for studies of vertebrate development and gene function.[2] They may supplement or replace higher vertebrate models, such as rats and mice. Pioneering work of George Streisinger at the University of Oregon established the zebrafish as a model organism; its importance was consolidated by large scale forward genetic screens (commonly referred to as the Tübingen/Boston screens). The scholarly journal Development devoted an issue to research using the fish in celebration of this landmark. [2] An online database of zebrafish genetic, genomic, and developmental information (ZFIN) has been established. D. rerio is one of the few species of fish to have been flown into space (see Animals in space).

A Zebrafish Pigment Mutant. The mutant called bleached blond was produced by insertional mutagenesis. The embryos in the picture are four days old. At the top is a wild-type embryo, below is the mutant. The mutant lacks black pigment in the melanocytes because it fails to synthesise melanin properly.
Enlarge
A Zebrafish Pigment Mutant. The mutant called bleached blond was produced by insertional mutagenesis. The embryos in the picture are four days old. At the top is a wild-type embryo, below is the mutant. The mutant lacks black pigment in the melanocytes because it fails to synthesise melanin properly.

Zebrafish embryonic development provides advantages over other vertebrate model organisms. Although the overall generation time of zebrafish is comparable to that of mice, zebrafish embryos develop rapidly, progressing from eggs to larvae in under three days. The embryos are large, robust, and transparent and develop externally to the mother, characteristics which all facilitate experimental manipulation and observation. [5] Their nearly constant size during early development facilitates simple staining techniques, and drugs may be administered by adding directly to the tank. Unfertilised eggs can be made to divide, and the two-celled embryo fused into a single cell, creating a fully homozygous embryo.

A common reverse genetics technique is to reduce gene expression or modify splicing in zebrafish using Morpholino antisense technology. Morpholino oligonucleotides are stable, synthetic macromolecules that contain the same bases as DNA or RNA; by binding to complementary RNA sequences, they reduce the expression of specific genes. The journal Genesis devoted an issue to research using Morpholino oligos[3], mostly in D. rerio. Morpholino oligonucleotides can be injected into one cell of a zebrafish embryo after the 32-cell stage, producing an organism in which gene expression is reduced in only the cells descended from the injected cell. However, cells in the early embryo (<32 cells) are interpermeable to large molecules[4], [5], allowing diffusion of Morpholinos between cells. A known problem with gene knockdowns in zebrafish is that, because the genome underwent a duplication after the divergence of ray-finned fishes and lobe-finned fishes, it is not always easy to silence the activity one of the two gene paralogs reliably due to complementation by the other paralog.

Despite the complications of the zebrafish genome a number of attempts have also been made to develop global platforms for analysis of both gene expression by microarrays and also promoter regulation using ChIP-on-chip.

Zebrafish have the ability to regenerate fins, skin, the heart and the brain (in larval stages). Zebrafish have also been found to regenerate photoreceptors and retinal neurons following injury. The mechanisms of this regeneration are unknown, but are currently being studied. Researchers frequently cut the dorsal and ventral tail fins and analyze their regrowth to test for mutations. This research is leading the scientific community in the understanding of healing/repair mechanisms in vertebrates.

The results of genetic engineering in these fishes have been used to produce the Glofish, an aquarium pet with fluorescent pigments. Other varieties include golden, sandy and long fin fish.

In December 2005, a study of the golden strain identified the gene responsible for the unusual pigmentation of this strain as SLC24A5, a solute carrier that appears to be required for melanin production, and confirmed its function with a Morpholino knockdown. The orthologous gene was then characterized in humans and a one base pair difference was found to segregate strongly between fair skinned Europeans and dark skinned Africans. [6] This study featured on the cover of the academic journal Science and demonstrates the power of zebrafish as a model organism in the relatively new field of comparative genomics.

In January 2007, Chinese researchers at Fudan University raised genetically modified fish that can detect estrogen pollution in lakes and rivers, showing environmental officials what waterways need to be treated for the substance, which is linked to male infertility. Song Houyan and Zhong Tao, two professors at Fudan's molecular medicine lab, spent three years cloning estrogen-sensitive genes and injecting them into the fertile eggs of zebrafish. The modified fish turn green if they are placed into water that is polluted by estrogen[7].


On August 1, 2007, British researchers said they had successfully grown in the laboratory a type of adult stem cell found in the eyes of both fish and mammals that develops into neurons in the retina.

In future, these cells could be injected into the eye as a treatment for diseases such as macular degeneration, glaucoma and diabetes-related blindness, according to Astrid Limb of University College London's (UCL) Institute of Ophthalmology.

Damage to the retina -- the part of the eye that sends messages to the brain -- is responsible for most cases of sight loss.

"Our findings have enormous potential," Limb said. "It could help in all diseases where the neurons are damaged, which is basically nearly every disease of the eye."

Limb and her colleagues studied so-called Mueller glial cells in the eyes of people aged from 18 months to 91 years and found they were able to develop them into all types of neurons found in the retina.

They were also able to grow them easily in the lab, they reported in the journal Stem Cells.

The cells have already been tested in rats with diseased retinas, where they successfully migrated into the retina and took on the characteristics of the surrounding neurons. Now the team is working on the same approach in humans.[8].

See also

References

  1. ^ Froese, R. and D. Pauly. Editors.. Danio rerio. FishBase. Retrieved on 2007-04-07.
  2. ^ a b c
  3. ^ Watanabe M, Iwashita M, Ishii M, Kurachi Y, Kawakami A, Kondo S, Okada N. (2006) Spot pattern of leopard Danio is caused by mutation in the zebrafish connexin41.8 gene. EMBO Report.7: 893-897.
  4. ^ Mills D (1993) Aquarium Fish Harper Collins ISBN 0-7322-5012-9
  5. ^ Dahm, Ralf (2006), "The Zebrafish Exposed", American Scientist 94 (5): pp. 446-453

Further reading

External links


Major model organisms in genetics
Lambda phage | E. coli | Chlamydomonas | Tetrahymena | Budding yeast | Fission yeast | Neurospora | Maize | Arabidopsis | Medicago truncatula | C. elegans | Drosophila | Zebrafish | Rat | Mouse

 
 

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Copyrights:

Animal Encyclopedia. Grzimek's Animal Life Encyclopedia. Copyright © 2005 by The Gale Group, Inc. All rights reserved.  Read more
Genetics Encyclopedia. Genetics. Copyright © 2003 by The Gale Group, Inc. All rights reserved.  Read more
Wikipedia. This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Zebrafish" Read more

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