Arabidopsis thaliana

From Free net encyclopedia

{{Taxobox | color = lightgreen | name = Thale Cress | image = Arabidopsis thaliana.jpg | image_width = 200px | regnum = Plantae | divisio = Magnoliophyta | classis = Magnoliopsida | ordo = Brassicales | familia = Brassicaceae | subfamilia = Brassicoideae | genus = Arabidopsis | species = A. thaliana | binomial = Arabidopsis thaliana | binomial_authority = (L.) Heynh. }}

Arabidopsis thaliana, commonly called arabidopsis, Thale Cress, or Mouse-ear Cress, a small flowering plant related to cabbage and mustard, is one of the model organisms for studying plant sciences, including genetics and plant development. It plays the role for plant science that mouse and fruit fly (Drosophila) play in human biology.

1 Model organism
2 History of arabidopsis as a model organism
3 Research
- 3.1 Non-mendelian inheritance
- 3.2 Light sensing
4 See also
5 References
6 External links

[edit]

Model organism

Although Arabidopsis thaliana has little agronomic significance, it has several advantages that made it the model for understanding the genetic, cellular and molecular biology of flowering plants.

The small size of its genome made it useful for genetic mapping and sequencing. At about 125 million base pairs and five chromosomes, it is a small genome for a plant species. It was the first sequenced plant genome, in 2000. Much work has been done to assign a function to the 25,500 genes so far found.

The plant's small size and rapid life cycle are also advantages. It takes about six weeks from germination to mature seed. Its small size is convenient for cultivation in a small space and it produces many seeds.

Finally, plant transformation in arabidopsis is easy, using Agrobacterium tumefaciens to transfer DNA to the plant genome.

[edit]

History of arabidopsis as a model organism

The first mutant in arabidopsis was documented by Alexander Braun in 1873. It is now known as AGAMOUS, and was cloned in 1990. Yet the potential of arabidopsis as a model organism was not documented until 1943.

Friedrich Laibach published the chromosome number of arabidopsis in 1907 and proposed it as a model organism in 1943. His student Erna Reinholz published her thesis on arabidopsis in 1945, describing the first collection of arabidopsis mutants that they generated using x-ray mutagenesis. Laibach continued his important contributions to arabidopsis research by collecting a large number of ecotypes. With the help of Albert Kranz, these were organised into the current ecotype collection of 750 natural accessions of Arabidopsis thaliana from around the world.

In the 1950s and 1960s John Langridge and George Rédei played an important role in establishing arabidopsis as a useful organism for biological laboratory experiments. Rédei wrote several scholarly reviews instrumental in introducing the model to the scientific community.

The start of the arabidopsis research community dates to a newsletter called Arabidopsis Information Service, established in 1964. The first International Arabidopsis Conference was held in 1965, in Göttingen, Germany.

In the 1980s arabidopsis started to become widely used in plant research laboratories around the world. It was one of several candidates that included maize, petunia and tobacco. The latter two were attractive since they were easily transformable, while maize was a well established genetic model for plant biology. The breakthrough year for arabidopsis as the preferred model plant came in 1986 when T-DNA mediated transformation was first published and this coincided with the first gene to be cloned and published.

[edit]

Research

[edit]

Non-mendelian inheritance

In 2005, scientists at Purdue University discovered in arabidopsis an alternative to previously known mechanisms of DNA repair, which one scientist called a "parallel path of inheritance". It was observed in mutations of the HOTHEAD gene. Plants mutant in this gene exhibit organ fusion, and pollen can germinate on all plant surfaces, not just the stigma. After spending over a year eliminating simpler explanations, it was indicated that the plants "cached" versions of their ancestors' genetic code going back at least four generations, and used these records as templates to correct the HOTHEAD mutation and other Single nucleotide polymorphisms. The initial hypothesis proposed that the record may be RNA-based (Lolle 2005). [1] Since then, alternative models have been proposed which would explain the phenotype without requiring a new model of inheritance (Chaudhury 2005)(Comai and Cartwright 2005). [2]

[edit]

Light sensing

The photoreceptors phytochrome A, B, C, D and E mediate red light based phototropic response. Understanding the function of these receptors has helped plant biologists understand the signalling cascades that regulate photoperiodism, germination, de-etiolation and shade avoidance in plants.

Arabidopsis was used extensively in the study of the genetic basis of phototropism, chloroplast alignment, and stomatal aperture and other blue light-influenced processes. These traits respond to blue light, which is perceived by the phototropin light receptors. Another blue light receptor, cryptochrome, is also know to function in arabidopsis and is especially important for light entrainment to control the plants circadian rhythms.

Light response was even found in roots, which were thought not to respond to light. While gravitropic response of arabidopsis root organs is their predominant tropic response, specimens treated with mutagens and selected for the absence of gravitropic action showed negative phototropic response to blue or white light, and positive response to red light.

[edit]

References

Lolle, S.J., Victor, J.L., Young, J.M., and Pruitt, R.E. (2005). Genome-wide non-mendelian inheritance of extra-genomic information in Arabidopsis. Nature 434, 505–509.

Chaudhury, A. (2005). Hothead healer and extragenomic information. Nature 437, E1–E2.

Comai, L. and Cartwright, R.A. (2005). A Toxic Mutator and Selection Alternative to the Non-Mendelian RNA Cache Hypothesis for hothead Reversion. The Plant Cell, 17 2856-2858

[edit]