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Zebrafish

 
 

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.

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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
Top
Danio rerio

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
  • Brachydanio rerio
  • Cyprinus chapalio
  • Cyprinus rerio
  • Danio frankei
  • Danio lineatus
  • Nuria rerio
  • Perilampus striatus
  • Zebra danio


The zebrafish, also known as Danio rerio, is a tropical freshwater fish belonging to the minnow family (Cyprinidae).[1] It is a popular aquarium fish, frequently sold under the trade name zebra danio, and is an important vertebrate model organism in scientific research.

Contents

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

Zebrafish have been introduced in aquariums in Japan, Canada, the United States and Australia.[3] They have also been sighted in Colombia, presumably having escaped from an aquarium.

Description

The fish is named for the five uniform, pigmented, horizontal blue stripes on the side of the body, all of which extend to the end of the caudal fin. Its shape can be described as fusiform and laterally compressed, with its mouth directed upwards. 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. Adult females will exhibit a small genital papilla in front of the anal fin origin. The zebrafish can grow to 6.4 centimetres (2.5 in), although it is uncommon for them to grow past 4 centimetres in captivity.

The approximate generation time for the Danio is 3–4 months. It has been observed that there must be a male present in order for ovulation and spawning of eggs to occur. Females are able to spawn as often as 2–3 days with hundreds of eggs being laid in each clutch. Upon release from the mother, developmental steps will be made, however without the presence of sperm growth will stop after the first few embryonic cleavages. Fertilized eggs will almost immediately become transparent, which is an important characteristic yielding D. rerio as a convenient research model[4]. Developement rapidly progresses, with precursors to all major organs appearing within 36 hours of fertilization. Hatching will take place anywhere from 48–72 hours post-fertilization, depending on the internal conditions of the embryo itself and the external temperature (ideally 28.5 °C). Swimming and feeding behavior are observed to occur approximately 72 hours post-fertilization. The sex of juvenile zebrafish cannot be distinguished except by dissection, and the genetic sex determinants are not clearly understood. The range of life-span for a zebrafish in captivity is around 2–3 years, although in ideal conditions, they may live up to 5 years.[4]

The zebrafish is omnivorous, and it primarily eats zooplankton, insects, and phytoplankton. It can eat a variety of foods if its main sources are not readily available.[4]

Varieties

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

The Leopard danio, previously known as Danio frankei, is a spotted colour morph of the zebrafish caused by a pigment mutation.[5] 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.[6]

Wild-Type Strains

The Zebra Fish Information Network [6] provides up-to-date information about current known Wild-Type strains of D. rerio. The most commonly found WT strains are: AB, TÜ, IN and WIK.

AB (AB)
AB/C32 (AB/C32)
AB/TL (AB/TL)
AB/Tuebingen (AB/TU)
C32 (C32)
Cologne (KOLN)
Darjeeling (DAR)
Ekkwill (EKW)

HK/AB (HK/AB)
HK/Sing (HK/SING)
Hong Kong (HK)
India (IND)
Indonesia (INDO)
Nadia (NA)
RIKEN WT (RW)
Singapore (SING)

SJA (SJA)
SJD (SJD)
SJD/C32 (SJD/C32)
Tuebingen (TU)
Tupfel long fin (TL)
Tupfel long fin nacre (TLN)
WIK (WIK)
WIK/AB (WIK/AB)

Hybrids

Hybrids between danios are common but they are sterile.

See link for photos of hybrids: http://www.nature.com/hdy/journal/v97/n3/fig_tab/6800867f1.html#figure-title

Brachydanio phylogenetic tree, see link: http://www.nature.com/hdy/journal/v97/n3/fig_tab/6800867f2.html#figure-title

Aquarium care

Zebrafish are hardy fish and considered good for beginner aquarists. Their ease of keeping and breeding, beauty, price, playful nature and broad availability all contribute to their popularity. They thrive best at temperatures above 22 °C (71.6 °F) and below 27 °C (80.6 °F). They feed on worms and small crustaceans and on insect larvae. They also thrive as shoals of six 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. Most Danios will accept common food flakes and tubifex worms. They are egglayers and as the female drops the eggs the male with fertilize them and within a few days the will hatch and some may be eaten by the parents unless the parents are in a separate tank or the eggs were scooped up into a breeder box or netted container.

Model organism for development and genetics

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 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. An online database of zebrafish genetic, genomic, and developmental information, the Zebrafish Information Network (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.

Research with D. rerio has allowed advances in the fields of developmental biology, oncology[7], toxicology[8], reproductive studies, teratology, genetics, neurobiology, environmental sciences, stem cell and regenerative medicine[9], and evolutionary theory[10]. Perhaps its greatest advantages for use in the laboratory as a model system come from its now sequenced genetic code, well understood, easily observable and testable developmental behaviors, and the availability of well-characterized mutants. Zebrafish embryonic development provides advantages over other vertebrate model organisms as well. 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. [11] Their nearly constant size during early development facilitates simple staining techniques, and drugs may be administered by adding directly to the tank. Unfertilized eggs can be made to divide, and the two-celled embryo fused into a single cell, creating a fully homozygous embryo.

See link for pigmentation mutants of D rerio: http://www.nature.com/hdy/journal/v97/n3/fig_tab/6800867f5.html#figure-title

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, 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,[12][13] 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 commercially available global platforms for analysis of both gene expression by microarrays and promoter regulation using ChIP-on-chip exist.

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.

Recent developments

In October 2001, researchers from the University of Oklahoma published the complete mitochondrial DNA sequence of D. rerio[14]. The length of the zebrafish mitochondrial genome is 16,596 base pairs. This is within 100 base pairs of other related species of fish, and it is notably only 18 bp longer than the goldfish (Carassius auratus) and 21 bp longer than the carp (Cyprinus carpio). The zebrafish gene order and content is identical to the common vertebrate form of mitochondrial DNA. It contains 13 protein-coding genes and a noncoding control region containing the origin of replication for the heavy strand. In between a grouping of five tRNA genes, a sequence resembling vertebrate origin of light strand replication is found. In comparing the nucleotide sequence to other vertebrates it is difficult to draw any evolutionary conclusions because it is difficult to determine as to whether base pair changes have adaptive significance.

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 appeared 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.[15] 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, 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.[16]

On August 1, 2007, researchers at University College London said they had grown in the laboratory a type of adult stem cell found in the eyes of fish and mammals that develops into neurons in the retina. These cells could be injected in the eye to treat all diseases where the retinal neurons are damaged — nearly every disease of the eye, including macular degeneration, glaucoma, and diabetes-related blindness. Damage to the retina — the part of the eye that sends messages to the brain — is responsible for most cases of sight loss. The researchers studied Müller glial cells in the eyes of humans aged from 18 months to 91 years and 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 were 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.[17]

In February 2008, researchers at Children's Hospital Boston reported in the journal Cell Stem Cell the development of a new strain of zebrafish, named Casper, with see-through bodies.[18] This allows for detailed visualization of individual blood stem cells and metastasizing (spreading) cancer cells within a living adult organism. Because the function of many genes are shared between fish and humans, this tool is expected to yield insight into human diseases such as leukemia and other cancers.[19][18]

In April 2009, Researchers at the Institute of Genomics and Integrative Biology, Delhi announced the sequencing of the wild-type strain of Zebrafish, complete with with about 1.7 billion genetic alphabets[20][21].

See also

References

  1. ^ Froese, R. and D. Pauly. Editors.. "Danio rerio". FishBase. http://www.fishbase.org/Summary/speciesSummary.php?ID=4653&genusname=Danio&speciesname=rerio. Retrieved on 2007-04-07. 
  2. ^ a b c Mayden, Richard L.; Tang, Kevin L.; Conway, Kevin W.; Freyhof, Jörg; Chamberlain, Sarah; Haskins, Miranda; Schneider, Leah; Sudkamp, Mitchell; Wood Robert M.; Agnew, Mary; Bufalino, Angelo; Sulaiman, Zohrah; Miya, Masaki; Saitoh, Kenji; He, Shunping (2007). "Phylogenetic relationships of Danio within the order Cypriniformes: a framework for comparative and evolutionary studies of a model species". J. Exp. Zool. (Mol. Dev. Evol.) 308B: 642–654. doi:10.1002/jez.b.21175. 
  3. ^ USGS NAS - Nonindigenous Aquatic Species
  4. ^ a b c Spence R, Gerlach G, Lawrence C, Smith C (February 2008). "The behaviour and ecology of the zebrafish, Danio rerio". Biological Reviews 83 (1): 13-34. PMID 18093234. 
  5. ^ Watanabe M, Iwashita M, Ishii M, et al. (September 2006). "Spot pattern of leopard Danio is caused by mutation in the zebrafish connexin41.8 gene". EMBO Rep. 7 (9): 893–7. doi:10.1038/sj.embor.7400757. PMID 16845369. 
  6. ^ Mills, Dick (1993). Eyewitness Hnbk Aquarium Fish. Harper Collins. ISBN 0-7322-5012-9. 
  7. ^ [1]Xiang J, et al. (Feb 2009). "Identifying Tumor Cell Growth Inhibitors by Combinatorial Chemistry and Zebrafish Assays". PLoS ONE 4 (2): e4361. PMID 19194508. 
  8. ^ [2]Hill AJ, Teraoka H, Heideman W & Peterson RE (Jul 2005). "Zebrafish as a Model Vertebrate for Investigating Chemical Toxicity". Toxicological Sciences 86 (1): 6-19. PMID 15703261. 
  9. ^ [3]Major RJ, Poss KD (2007). "Zebrafish heart regeneration as a model for cardiac tissue repair". Drug Discov Today Dis Models 4 (4): 219-225. PMID 19081827. 
  10. ^ [4]Parichy, DM (Sep 2006). "Evolution of danio pigment pattern development". Heredity 97: 200-210. PMID 16835593. 
  11. ^ Dahm, Ralf (2006), "The Zebrafish Exposed", American Scientist 94 (5): 446–453 
  12. ^ Kimmel CB, Law RD (Mar 1985). "Cell lineage of zebrafish blastomeres. I. Cleavage pattern and cytoplasmic bridges between cells". Dev Biol. 108 (1): 78–85. doi:10.1016/0012-1606(85)90010-7. PMID 3972182. http://linkinghub.elsevier.com/retrieve/pii/0012-1606(85)90010-7. 
  13. ^ Kimmel CB, Law RD (Mar 1985). "Cell lineage of zebrafish blastomeres. III. Clonal analyses of the blastula and gastrula stages". Dev Biol. 108 (1): 94–101. doi:10.1016/0012-1606(85)90012-0. PMID 3972184. http://linkinghub.elsevier.com/retrieve/pii/0012-1606(85)90012-0. 
  14. ^ [5]Broughton RE, Milam JE, Roe BA (October 2001). "The complete sequence of the zebrafish (Danio rerio) mitochondrial genome and evolutionary patterns in vertebrate mitochondrial DNA". Genome Res 11: 1958–67. PMID 11691861. 
  15. ^ Lamason RL, Mohideen MA, Mest JR, et al. (Dec 2005). "SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans". Science 310 (5755): 1782–6. doi:10.1126/science.1116238. PMID 16357253. 
  16. ^ Fudan scientists turn fish into estrogen alerts
  17. ^ news.yahoo
  18. ^ a b White RM, Sessa A, Burke C, et al. (Feb 2008). "Transparent adult zebrafish as a tool for in vivo transplantation analysis". Cell Stem Cell 2 (2): 183–9. doi:10.1016/j.stem.2007.11.002. PMID 18371439. 
  19. ^ livescience.com
  20. ^ Decoding the Genome Mystery Indian Express, Jul 05, 2009.
  21. ^ Genome@IGIB Institute of Genomics and Integrative Biology (IGIB)

Further reading

External links


 
 

 

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