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Drosophila sechellia
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Arthropoda
Class:	Insecta
Order:	Diptera
Family:	Drosophilidae
Genus:	Drosophila
Subgenus:	Sophophora
Species group:	melanogaster
Species subgroup:	melanogaster
Species complex:	simulans
Species:	D. sechellia
Binomial name
Drosophila sechellia Tsacas and Baechli, 1981

Drosophila sechellia is a species of fruit fly, used in lab studies of speciation because it can mate with Drosophila simulans.

Drosophila sechellia is endemic to (some of) the Seychelles, and was one of 12 fruit fly genomes sequenced for a large comparative study.

Morinda fruit

Drosophila sechellia are known to preferentially lay eggs on toxic Morinda fruits.

The resistance that the D. sechellia shows to the fruit’s toxins is due to its attraction to the ripe Morinda through its octanoic acid. The presence of this fruit is said to help stimulate egg production, which can be attributed to evolutionary adaptive traits. A plausible evolutionary explanation to this attraction is that, upon its arrival in the Seychelles, the ancestor of Drosophila sechellia used a diversity of resources available such as aged, rotten, and nontoxic Morinda fruits.

Research has shown that a mutation in the gene that inhibits egg production is associated with a reduction in L-DOPA; L-DOPA is a precursor of the fertility-regulating hormone dopamine. Morinda fruits are rich in L-DOPA, owing to their usually insecticidal capacities. Drosophila sechellia fertility is reliant on the L-DOPA found in Morinda fruit, and as a result Drosophila sechellia reproduces solely on these toxic fruits. Recent research found that reduced expression of a newly discovered gene, Esterase 6 (Est6), is an important element of the genetic underpinnings behind the adaptation of D. Sechellia to feed on Morinda fruits.

Compared to other species and close relatives, the D. sechellia is found to have lower female adult reproductive potential, as it is shown to produce fewer ovarioles than the D. simulans, but also produces large eggs. This can lead to the evidence in which the evolution of ovoviviparity in D. sechellia is a result to avoid competition and possible exploitation of an unoccupied niche. An evolutionary hypothesis proposed by Mueller & Bitner (2015) is that during the initial phases of ovoviviparity, the more rapidly developing genotypes could not begin development at the peak of octanoic acid concentration despite requiring degradation. This can be due to its tolerance only slightly increasing relative to the other slower developing genotypes. The rapid developing genotypes thus only had a short time to grow on the Morinda fruit before the arrival of other strong larval competitors.

This adaptation to the fresh Morinda fruit would require toleration to the toxins and would make the D. sechellia larvae develop quickly after the eggs were deposited. Its ovoviviparity would ensure that eggs hatch almost immediately in the chosen environment, like a fresh Morinda fruit, and virtually be competitor free until the fruit becomes rotten. The tolerance is a consequence of the changing biotic community in the Morinda fruit as it decays, and expects that such a mutation would accelerate the process of adaptation.

References

1. Drosophila 12 Genomes Consortium; et al. (2007). "Evolution of genes and genomes on the Drosophila phylogeny". Nature. 450 (7167): 203–218. Bibcode:2007Natur.450..203C. doi:10.1038/nature06341. PMID 17994087.{{cite journal}}: CS1 maint: numeric names: authors list (link)
2. Jones, C. D. (2005, February). Genetica. The genetics of adaptation in Drosophila sechellia, 123, 139. https://doi.org/10.1007/s10709-004-2728-6
3. RHKA, S., CAPY, P., & DAVID, J. (1991, March). PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. Host-plant specialization in the Drosophila melanogaster species complex: a physiological, behavioral, and genetical analysis., 88(5), 1835-1839. https://doi.org/10.1073/pnas.88.5.1835
4. "Toxic fruits hold the key to reproductive success". Max-Planck-Gesellschaft. December 9, 2014.
5. Stephen M. Lanno, Ivy Lam; Zachary Drum; Samuel C. Linde; Sara M. Gregory; Serena J. Shimshak; Mariel V. Becker; Kerry E. Brew; Aashli Budhiraja; Eliza A. Carter; Lorencia Chigweshe; Keagan P. Collins; Timothy Earley; Hannah L. Einstein; Angela A. Fan; Sarah S. Goss; Eric R. Hagen; Sarah B. Hutcheon; Timothy T. Kim; Mackenzie A. Mitchell; Nola R. Neri; Sean E. Patterson; Gregory Ransom; Guadalupe J. Sanchez; Bella M. Weiner; Dacheng Zhao & Joseph D. Coolon (1 October 2019). "Genomics Analysis of L-DOPA Exposure in Drosophila sechellia.". G3: Genes, Genomes, Genetics. 9 (12): 3973–3980. doi:10.1534/g3.119.400552. PMC 6893205. PMID 31575638.
6. Mueller, L. D., & Bitner, K. (2015, December). The American Naturalist (D. N. Reznick & S. Kalisz, Eds.). The Evolution of Ovoviviparity in a Temporally Varying Environment, 186(6), 711. 10.1086/683661
7. Mueller, L. D., & Bitner, K. (2015, December). The American Naturalist (D. N. Reznick & S. Kalisz, Eds.). The Evolution of Ovoviviparity in a Temporally Varying Environment, 186(6), 708-715. 10.1086/683661
8. Mueller, L. D., & Bitner, K. (2015, December). The American Naturalist (D. N. Reznick & S. Kalisz, Eds.). The Evolution of Ovoviviparity in a Temporally Varying Environment, 186(6), 714. 10.1086/683661

External links

• Drosophila sechellia at FlyBase
• Drosophila sechellia at Ensembl Genomes Metazoa
• View the droSec1 genome assembly in the UCSC Genome Browser

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