Blog Post 3 - Batesian Mimicry in Papilio polytes
Katoh, M., Tatsuta, H. and Tsuji, K., 2018. Ultraviolet exposure has an epigenetic effect on a Batesian mimetic trait in the butterfly Papilio polytes. Scientific reports, 8(1), p.13416.
This week I will be using the
swallowtail butterfly, Papilio polytes,
as an example of Batesian mimcry. The swallowtail butterfly is common
throughout Asia and is known to resemble the unpalatable red bodied
butterfly, Pachliopta aristolochiae (Katoh
et al. 2017). In the swallowtail butterfly there is a single male isoform and two different female
isoforms; Interestingly, only the female forms can mimic the red bodied
butterfly (Nishikawa et al.
2015). Females occur
either in the form of: 1 - A male-like, black and white non-mimetic form (Katoh et al.
2017) OR 2- As a red-spotted form that mimics a toxic
species (i.e. the red bodied butterfly) (Katoh et al. 2017)
This female limited mimicry is maternally heritable (Katoh et al. 2018) and is believed that single-locus Mendelian inheritance coded
by the autosomal doublesex (dsx) supergene, with mimetic alleles (H) dominant
to the non-mimetic allele (h), controls this polymorphism (Katoh et al. 2017). So mimicry in P. polytes is affected by a single gene, being the dsx, where the H locus is tracked to a sex
determining gene (Mallet 2015). Functional tests of the mimetic allele of the
dsx(H) locus have been carried out and imply that it plays a role in changing wing coloration from a non-mimetic to a mimetic
pattern (Nishikawa et al.
2015).
An interesting factor
to look at is what drives the evolution of this mimicry. As stated in my last
post, Batesian mimicry occurs in two steps. First, a major
mutation of large affect produces a rough resemblance to the model, then, fine tuning of the
mimic’s appearance toward the model through fixation of “modifier” alleles.
Mutations can arise spontaneously at low frequencies due to chemical instabilities
and errors during DNA replication (Lodish et
al. 2000). They can also occur in organisms through natural exposure to certain
environmental factors (Lodish et al.
2000). Micro-evolution
towards better mimicry in the P. polytes has been influenced by
selection pressures such as the arrival of a new model species, predation
pressures and exposure to ultraviolet (UV) light (Katoh et al. 2017; Katoh
et al. 2018). UV irradiation has been found to damage exposed tissues and damaged
wings can reduce reproductive success (Katoh et al. 2018). Melanin is what
many organisms use to protect themselves against UV irradiation and in the P. polytes it is the black
pigment in the wings (Katoh et al. 2018). A
negative correlation between UV irradiation and red spot size has been observed
in the species suggesting a conflict between protecting against UV damage and
avoiding predation (Katoh et al. 2018).
References
Katoh, M., Tatsuta, H. and Tsuji, K., 2017. Rapid evolution of a
Batesian mimicry trait in a butterfly responding to arrival of a new model. Scientific
reports, 7(1), p.6369.
Katoh, M., Tatsuta, H. and Tsuji, K., 2018. Ultraviolet exposure has an epigenetic effect on a Batesian mimetic trait in the butterfly Papilio polytes. Scientific reports, 8(1), p.13416.
Lodish H, Berk A, Zipursky SL, et al. 2000. Section 8.1, Mutations: types
and causes. Molecular
Cell Biology 4th edition.
Mallet, J., 2015. New genomes
clarify mimicry evolution. Nature genetics, 47(4), p.306.
Nishikawa, H., Iijima, T., Kajitani, R., Yamaguchi, J., Ando, T., Suzuki, Y., Sugano, S., Fujiyama, A., Kosugi, S., Hirakawa, H. and Tabata, S., 2015. A genetic mechanism for female-limited Batesian mimicry in Papilio butterfly. Nature genetics, 47(4), p.405.
Nishikawa, H., Iijima, T., Kajitani, R., Yamaguchi, J., Ando, T., Suzuki, Y., Sugano, S., Fujiyama, A., Kosugi, S., Hirakawa, H. and Tabata, S., 2015. A genetic mechanism for female-limited Batesian mimicry in Papilio butterfly. Nature genetics, 47(4), p.405.
It’s so cool that this change is caused by a single gene. Are there examples of other mimetic species that show this same genetic shift?
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