|This image is courtesy of Sarah Farrington of the
Center for Cancer Research at MIT. It comes from the home page of ZFIN ("Zebrafish Information Network"): http://zfin.org/cgi-bin/webdriver?MIval=aa-ZDB_home.apg|
The zebrafish, Danio rerio, has become another popular "model" organism with which to study fundamental biological questions.
It is a small (1–1.5 inches)(2.5–3.8 cm) freshwater fish that grows easily in aquaria (it is available at many pet stores).
Some of its advantages for biologists:
- It breeds early and often (daily).
- It is a vertebrate, like us, and thus can provide clues to human biology that invertebrates like Drosophila and Caenorhabditis elegans may not.
- Its embryos, like those of most fishes, develop outside the body where they can be easily observed (unlike mice).
- Its embryos are transparent so defects in development can be seen easily.
- Individual cells in the embryo can be labeled with a fluorescent dye and their fate followed.
- Embryonic development is quick (they hatch in two days).
- They can absorb small molecules, such as mutagens, from the aquarium water.
- Individual cells — or clusters of cells — can be transplanted to other locations in the embryo (as Mangold did with newt embryos — Link).
- They can be forced to develop by parthenogenesis to produce at will homozygous animals with either:
- a male-derived or
- female-derived genome.
- They can be cloned from somatic cells.
- They can be made transgenic (like mice and Drosophila)
- Its genome (1.4 x 109 base pairs) has been sequenced revealing 26,606 protein-coding genes.
"Forward" and "Reverse" Genetics
Since Mendel's time, most genetics has involved
- observing an interesting phenotype
- tracking down the gene responsible for it.
So this "forward" genetics proceeds from phenotype -> genotype.
Some examples in these pages:
These methods have been called "forward" genetics to distinguish them from a more recent approach, which has become an urgent priority with the successes of genome sequencing.
Rapid methods of DNA sequencing has generated a vast amount of data.
Thousands of suspected genes have been revealed (e.g., finding open reading frames — ORFs), but the function of many of them is still unknown.
But now with
- a knowledge of the DNA sequence of a gene of unknown function,
- one can use methods for suppressing that particular gene ("knockdown"), and then
- observe the effect on the phenotype.
So this "reverse" genetics proceeds from genotype -> phenotype.
Reverse genetics has been applied successfully to
For example, the function of a mysterious gene sequence in Danio can be studied by
- synthesizing a short antisense oligonucleotide complementary to a section of the gene.
- The oligonucleotide is chemically-modified to make it more stable than a fragment of RNA.
- Binding to its complementary sequence on the messenger RNA (mRNA) produced by transcription of the animal's gene, blocks ("knocks down") gene expression by
Because we share so many similar gene sequences (orthologous genes) with Danio, if one can discover the function of the gene in Danio, then we have a better idea of the role of its ortholog in humans.
3 May 2013