Drosophila melanogaster

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Drosophila melanogaster
Male Drosophila melanogaster
Male Drosophila melanogaster
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Diptera
Family: Drosophilidae
Subfamily: Drosophilinae
Genus: Drosophila
Subgenus: Sophophora
Species group: melanogaster group
Species subgroup: melanogaster subgroup
Species complex: melanogaster complex
Species: D. melanogaster
Binomial name
Drosophila melanogaster
Meigen, 1830[1]

Drosophila melanogaster (from the Greek for black-bellied dew-lover) is a two-winged insect that belongs to the Diptera, the order of the flies. The species is commonly known as the common fruit fly, and is one of the most commonly used model organisms in biology, including studies in genetics, physiology and life history evolution. Flies belonging to the Tephritidae are also called fruit flies, which can lead to confusion, especially in Australia where the term fruit fly is used to refer to the Tephritidae, an economic pest in fruit production.

Contents

[edit] Physical appearance

Male (left) and female D. melanogaster
Male (left) and female D. melanogaster

Wildtype fruit flies have brick red eyes, are yellow-brown in colour, and have transverse black rings across their abdomen. They exhibit sexual dimorphism: females are about 2.5 millimetres (0.1 inches) long; males are slightly smaller and the back of their bodies is darker. Males are easily distinguished from females based on colour differences, with a distinct black patch at the abdomen, less noticeable in recently emerged flies (see fig), and the sexcombs (a row of dark bristles on the tarsus of the first leg). Furthermore, males have a cluster of spiky hairs (claspers) surrounding the reproducing parts used to attach to the female during mating. There are extensive images at Fly Base.

[edit] Life cycle

Egg of D. melanogaster
Egg of D. melanogaster

The D. melanogaster lifespan is about 30 days at 29 °C (84 °F).

The developmental period for Drosophila melanogaster varies with temperature, as with many ectothermic species. The shortest development time (egg to adult), 7 days, is achieved at 28 °C (82 °F).[2][3] Development times increase at higher temperatures (30 °C (86 °F), 11 days) due to heat stress. Under ideal conditions, the development time at 25 °C (77 °F) is 8.5 days,[4][2][3] at 18 °C (64 °F) it takes 19 days[2][3] and at 12 °C (54 °F) it takes over 50 days.[2][3] Under crowded conditions, development time increases,[5] while the emerging flies are smaller.[5][6] Females lay some 400 eggs (embryos), about five at a time, into rotting fruit or other suitable material such as decaying mushrooms and sap fluxes. The eggs, which are about 0.5 millimetres long, hatch after 12–15 h (at 25 °C (77 °F)).[2][3] The resulting larvae grow for about 4 days (at 25 °C) while molting twice (into 2nd- and 3rd-instar larvae), at about 24 and 48 h after eclosion.[2][3] During this time, they feed on the microorganisms that decompose the fruit, as well as on the sugar of the fruit itself. Then the larvae encapsulate in the puparium and undergo a four-day-long metamorphosis (at 25 °C), after which the adults eclose (emerge).[2][3]

Mating fruit flies. Note sexcombs male insert
Mating fruit flies. Note sexcombs male insert

Females become receptive to courting males at about 8-12 hours after emergence.[7] Males perform a sequence of five behavioral patterns to court females. First, males orient themselves while playing a courtship song by horizontally extending and vibrating their wings. Soon after, the male positions itself at the rear of the female's abdomen in a low posture to tap and lick the female genitalia. Finally, the male curls its abdomen, and attempts copulation. Females can reject males by moving away and extruding their ovipositor. The average duration of successful copulation is 30 minutes, during which males transfer a few hundred very long (1.76mm) sperm cells in seminal fluid to the female.[8] Females store the sperm, which may need to compete with other males' stored sperm to fertilize eggs.

[edit] Model organism in genetics

D. melanogaster types (clockwise): brown eyes with black body, cinnabar eyes, sepia eyes with ebony body, vermilion eyes, white eyes, and wild-type eyes with yellow body.
D. melanogaster types (clockwise): brown eyes with black body, cinnabar eyes, sepia eyes with ebony body, vermilion eyes, white eyes, and wild-type eyes with yellow body.
Drosophila melanogaster mutation: yellow cross-veinless forked fruit fly.
Drosophila melanogaster mutation: yellow cross-veinless forked fruit fly.
A wild fruit fly (left) has antennae, while a fly with the antennapedia mutation (right) has an extra set of feet in the place of antennae.
A wild fruit fly (left) has antennae, while a fly with the antennapedia mutation (right) has an extra set of feet in the place of antennae.

Drosophila melanogaster is the most studied organism in biological research, particularly in genetics and developmental biology. There are several reasons:

  • It is small and easy to grow in the laboratory.
  • It has a short generation time (about two weeks) and high fecundity (females can lay >800 eggs in life time i.e. one egg per 30 min with enough food).
  • The mature larvae show giant chromosomes in the salivary glands called polytene chromosomes—"puffs" indicate regions of transcription and hence gene activity.
  • It has only four pairs of chromosomes: three autosomes, and one sex chromosome.
  • Males do not show meiotic recombination, facilitating genetic studies.
  • Genetic transformation techniques have been available since 1987.
  • Its compact genome was sequenced and first published in 2000.[9]

Charles W. Woodworth is credited with being the first to breed Drosophila in quantity and for suggesting to W. E. Castle that they might be used for genetic research during his time at Harvard University. Beginning in 1910, fruit flies helped Thomas Hunt Morgan accomplish his studies on heredity. "Thomas Hunt Morgan and colleagues extended Mendel's work by describing X-linked inheritance and by showing that genes located on the same chromosome do not show independent assortment. Studies of X-linked traits helped confirm that genes are found on chromosomes, while studies of linked traits led to the first maps showing the locations of genetic loci on chromosomes" (Freman 214). The first maps of Drosophila chromosomes were completed by Alfred Sturtevant.

[edit] Genome

The genome of D. melanogaster (sequenced in 2000, and curated at the FlyBase database[9]) contains four pairs of chromosomes: an X/Y pair, and three autosomes labeled 2, 3, and 4. The fourth chromosome is so tiny that it is often ignored, aside from its important eyeless gene. Its sequenced genome of 120 million base pairs has been annotated[9] and contains approximately 13,767 protein-coding genes which comprise ~20% of the genome. More than 60% of the genome appears to be functional non-protein-coding DNA[10] involved in gene expression control. Determination of sex in Drosophila occurs by the ratio of X chromosomes to autosomes, not because of the presence of a Y chromosome as in human sex determination.

Drosophila genes are traditionally named after the phenotype they cause when mutated. For example, the absence of a particular gene in Drosophila will result in a mutant embryo that does not develop a heart. Scientists have thus called this gene tinman, named after the Oz character of the same name (Cf. Azpiazu & Frasch (1993) Genes and Development: 7: 1325-1340.). This system of nomenclature results in a wider range of gene names than in other organisms.

[edit] Similarity to humans

About 75% of known human disease genes have a recognizable match in the genetic code of fruit flies (Reiter et al (2001) Genome Research: 11(6):1114-25), and 50% of fly protein sequences have mammalian analogues. An online database called Homophila [1] is available to search for human disease gene homologues in flies and vice versa. Drosophila is being used as a genetic model for several human diseases including the neurodegenerative disorders Parkinson's, Huntington's, spinocerebellar ataxia and Alzheimer's disease. The fly is also being used to study mechanisms underlying aging and oxidative stress, immunity, diabetes, and cancer, as well as drug abuse.

[edit] Development

Main article: Drosophila embryogenesis

Embryogenesis in Drosophila has been extensively studied, as its small size, short generation time, and large brood size makes it ideal for genetic studies. It is also unique among model organisms in that cleavage occurs in a syncytium.

Drosophila melanogaster oogenesis
Drosophila melanogaster oogenesis

During oogenesis, cytoplasmic bridges called "ring canals" connect the forming oocyte to nurse cells. Nutrients and developmental control molecules move from the nurse cells into the oocyte. In the figure to the left, the forming oocyte can be seen to be covered by follicular support cells.

After fertilization of the oocyte the early embryo or (syncytial embryo) undergoes rapid DNA replication and 13 nuclear divisions until approximately 5000 to 6000 nuclei accumulate in the unseparated cytoplasm of the embryo. By the end of the 8th division most nuclei have migrated to the surface, surrounding the yolk sac (leaving behind only a few nuclei, which will become the yolk nuclei). After the 10th division the pole cells form at the posterior end of the embryo, segregating the germ line from the syncytium. Finally, after the 13th division cell membranes slowly invaginate, dividing the syncytium into individual somatic cells. Once this process is completed gastrulation starts.

Nuclear division in the early Drosophila embryo happens so quickly there are no proper checkpoints so mistakes may be made in division of the DNA. To get around this problem the nuclei which have made a mistake detach from their centrosomes and fall into the centre of the embryo (yolk sac) which will not form part of the fly.

The gene network (transcriptional and protein interactions) governing the early development of the fruitfly embryo is one of the best understood gene networks to date, especially the patterning along the antero-posterior (AP) and dorso-ventral (DV) axes (See under morphogenesis).

The embryo undergoes well-characterized morphogenetic movements during gastrulation and early development, including germ-band extension, formation of several furrows, ventral invagination of the mesoderm, posterior and anterior invagination of endoderm (gut), as well as extensive body segmentation[11] until finally hatching from the surrounding cuticle into a 1st-instar larva.

During larval development, tissues known as imaginal discs grow inside the larva. Imaginal discs develop to form most structures of the adult body, such as the head, legs, wings, thorax and genetalia. Cells of the imaginal disks are set aside during embryogenesis and continue to grow and divide during the larval stages - unlike most other cells of the larva which have differentiated to perform specialized functions and grow without further cell division. At metamorphosis, the larva forms a pupa, inside which the larval tissues are reabsorbed and the imaginal tissues undergo extensive morphogenetic movements to form adult structures.

[edit] Behavioral genetics and neuroscience

In 1971, Ron Konopka and Seymour Benzer published "Clock mutants of Drosophila melanogaster", a paper describing the first mutations that affected an animal's behavior. Wild-type flies show an activity rhythm with a frequency of about a day (24 hours). They found mutants with faster and slower rhythms as well as broken rhythms - flies that move and rest in random spurts. Work over the following 30 years has shown that these mutations (and others like them) affect a group of genes and their products that comprise a biochemical or biological clock. This clock is found in a wide range of fly cells, but the clock-bearing cells that control activity are several dozen neurons in the fly's central brain.

Since then, Benzer and others have used behavioral screens to isolate genes involved in vision, olfaction, audition, learning/memory, courtship, pain and other processes, such as longevity.

The first learning and memory mutants (dunce, rutabaga etc) were isolated by William "Chip" Quinn while in Benzer's lab, and were eventually shown to encode components of an intracellular signaling pathway involving cyclic AMP, protein kinase A and a transcription factor known as CREB. These molecules were shown to be also involved in synaptic plasticity in Aplysia and mammals.

Male flies sing to the females during courtship using their wing to generate sound, and some of the genetics of sexual behavior have been characterized. In particular, the fruitless gene has several different splice forms, and male flies expressing female splice forms have female-like behavior and vice-versa.

Furthermore, Drosophila has been used in neuropharmacological research, including studies of cocaine and alcohol consumption.

[edit] Vision

Stereo images of the fly eye
Stereo images of the fly eye

The compound eye of the fruit fly contains 760 unit eyes or ommatidia, and are one of the most advanced among insects. Each ommatidium contains 8 photoreceptor cells (R1-8), support cells, pigment cells, and a cornea. Wild-type flies have reddish pigment cells, which serve to absorb excess blue light so the fly isn't blinded by ambient light.

Each photoreceptor cell consists of two main sections, the cell body and the rhabdomere. The cell body contains the nucleus while the 100-μm-long rhabdomere is made up of toothbrush-like stacks of membrane called microvilli. Each microvillus is 1–2 μm in length and ~60 nm in diameter.[12] The membrane of the rhabdomere is packed with about 100 million rhodopsin molecules, the visual protein that absorbs light. The rest of the visual proteins are also tightly packed into the microvillar space, leaving little room for cytoplasm.

The photoreceptors in Drosophila express a variety of rhodopsin isoforms. The R1-R6 photoreceptor cells express Rhodopsin1 (Rh1) which absorbs blue light (480 nm). The R7 and R8 cells express a combination of either Rh3 or Rh4 which absorb UV light (345 nm and 375 nm), and Rh5 or Rh6 which absorb blue (437 nm) and green (508 nm) light respectively. Each rhodopsin molecule consists of an opsin protein covalently linked to a carotenoid chromophore, 11-cis-3-hydroxyretinal.[13]

Expression of Rhodopsin1 (Rh1) in photoreceptors R1-R6
Expression of Rhodopsin1 (Rh1) in photoreceptors R1-R6

As in vertebrate vision, visual transduction in invertebrates occurs via a G protein-coupled pathway. However, in vertebrates the G protein is transducin, while the G protein in invertebrates is Gq (dgq in Drosophila). When rhodopsin (Rh) absorbs a photon of light its chromophore, 11-cis-3-hydroxyretinal, is isomerized to all-trans-3-hydroxyretinal. Rh undergoes a conformational change into its active form, metarhodopsin. Metarhodopsin activates Gq, which in turn activates a phospholipase Cβ (PLCβ) known as NorpA.

PLCβ hydrolyzes phosphatidylinositol (4,5)-bisphosphate (PIP2), a phospholipid found in the cell membrane, into soluble inositol triphosphate (IP3) and diacylgycerol (DAG), which stays in the cell membrane. DAG or a derivative of DAG causes a calcium selective ion channel known as TRP (transient receptor potential) to open and calcium and sodium flows into the cell. IP3 is thought to bind to IP3 receptors in the subrhabdomeric cisternae, an extension of the endoplasmic reticulum, and cause release of calcium, but this process doesn't seem to be essential for normal vision.[14]

Calcium binds to proteins such as calmodulin (CaM) and an eye-specific protein kinase C (PKC) known as InaC. These proteins interact with other proteins and have been shown to be necessary for shut off of the light response. In addition, proteins called arrestins bind metarhodopsin and prevent it from activating more Gq.

A sodium/calcium exchanger known as CalX pumps the calcium out of the cell. It uses the inward sodium gradient to export calcium at a stoichiometry of 3 Na+/ 1 Ca++.[15]

TRP, InaC, and PLC form a signaling complex by binding a scaffolding protein called InaD. InaD contains five binding domains called PDZ domain proteins which specifically bind the C termini of target proteins. Disruption of the complex by mutations in either the PDZ domains or the target proteins reduces the efficiency of signaling. For example, disruption of the interaction between InaC, the protein kinase C, and InaD results in a delay in inactivation of the light response.

Unlike vertebrate metarhodopsin, invertebrate metarhodopsin can be converted back into rhodopsin by absorbing a photon of orange light (580 nm).

Approximately two-thirds of the Drosophila brain (about 200,000 neurons total) is dedicated to visual processing. Although the spatial resolution of their vision is significantly worse than that of humans, their temporal resolution is approximately ten times better.

[edit] Flight

The wings of a fly are capable of beating at up to 220 times per second. Flies fly via straight sequences of movement interspersed by rapid turns called saccades. During these turns, a fly is able to rotate 90 degrees in fewer than 50 milliseconds.

It was long thought that the characteristics of Drosophila flight were dominated by the viscosity of the air, rather than the inertia of the fly body. However, research in the lab of Michael Dickinson has indicated that flies perform banked turns, where the fly accelerates, slows down while turning, and accelerates again at the end of the turn. This indicates that inertia is the dominant force, as is the case with larger flying animals.[16]

[edit] See also

[edit] References

  1. ^ Meigen JW (1830). Systematische Beschreibung der bekannten europäischen zweiflügeligen Insekten. (Volume 6) (in German). Schulz-Wundermann. 
  2. ^ a b c d e f g Ashburner M, Thompson JN (1978). The laboratory culture of Drosophila. In: The genetics and biology of Drosophila. (Ashburner M, Wright TRF (eds.)). Academic Press, volume 2A: pp. 1–81. 
  3. ^ a b c d e f g Ashburner M, Golic KG, Hawley RS (2005). Drosophila: A Laboratory Handbook., 2nd ed., Cold Spring Harbor Laboratory Press, pp. 162–4. ISBN 0879697067. 
  4. ^ Bloomington Drosophila Stock Center at Indiana University: Basic Methods of Culturing Drosophila
  5. ^ a b Chiang HC, Hodson AC (1950). "An analytical study of population growth in Drosophila melanogaster.". Ecological Monographs 20: 173–206. 
  6. ^ Bakker K (1961). "An analysis of factors which determine success in competition for food among larvae of Drosophila melanogaster.". Archives Neerlandaises de Zoologie 14: 200–81. 
  7. ^ Pitnick S (1996). "Investment in testes and the cost of making long sperm in Drosophila.". American Naturalist 148: 57–80. 
  8. ^ http://8e.devbio.com/article.php?ch=9&id=87
  9. ^ a b c Adams MD, Celniker SE, Holt RA, et al (2000). "The genome sequence of Drosophila melanogaster". Science 287 (5461): 2185–95. doi:10.1126/science.287.5461.2185. PMID 10731132. 
  10. ^ Halligan DL, Keightley PD (2006). "Ubiquitous selective constraints in the Drosophila genome revealed by a genome-wide interspecies comparison". Genome Res. 16 (7): 875–84. doi:10.1101/gr.5022906. PMID 16751341. 
  11. ^ FlyMove website
  12. ^ Hardie RC, Raghu P (2001). "Visual transduction in Drosophila". Nature 413 (6852): 186–93. doi:10.1038/35093002. PMID 11557987. 
  13. ^ Nichols R, Pak WL (1985). "Characterization of Drosophila melanogaster rhodopsin". J. Biol. Chem. 260 (23): 12670–4. PMID 3930500. 
  14. ^ Raghu P, Colley NJ, Webel R, et al (2000). "Normal phototransduction in Drosophila photoreceptors lacking an InsP(3) receptor gene". Mol. Cell. Neurosci. 15 (5): 429–45. doi:10.1006/mcne.2000.0846. PMID 10833300. 
  15. ^ Wang T,Xu H,Oberwinkler J,GU Y, Hardie R, Montell C, et al (2005). "Light activation, adaptation, and cell survival Functions of the Na+/Ca2+ exchanger CalX". Neuron 45 (3): 367-378. doi:10.1016/j.neuron.2004.12.046. PMID 15694299. 
  16. ^ Caltech Press Release 4/17/2003

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Major model organisms in genetics