Parthenogenesis in squamata

Parthenogenesis is a mode of asexual reproduction in which offspring are produced by females without the genetic contribution of a male. Among all the sexual vertebrates, the only examples of true parthenogenesis, in which all-female populations reproduce without the involvement of males, are found in squamate reptiles (snakes and lizards).[1] There are about 50 species of lizard and 1 species of snake that reproduce solely through parthenogenesis (obligate parthenogenesis).[2] It is unknown how many sexually reproducing species are also capable of parthenogenesis in the absence of males (facultative parthenogenesis), but recent research has revealed that this ability is widespread among squamates.

Mechanisms

Parthenogenesis can result from either full cloning of the mother's genome, or through the combination of haploid genomes to create a "half-clone". Both mechanisms of parthenogenesis are seen in reptiles.

Full-cloning

Females can produce full clones of themselves through a modification of the normal meiosis process used to produce haploid egg cells for sexual reproduction. The female's germ cells undergo a process of premeiotic genome doubling, or endoreduplication, so that two consecutive division cycles in the process of meoisis result in a diploid, rather than haploid, genome. Whereas homologous chromosomes pair and separate during meiosis I in sexual species, identical duplicate sister chromosomes, produced through premeiotic replication, pair and separate during meiosis I in true parthenotes.[3] Pairing of identical sister chromosomes, in comparison to the alternative of pairing homologous chromosomes, maintains heterozygosity in obligate parthenotes. Meiosis II involves the separation of sister chromatids in both sexual and parthenogenetic species. This method of parthenogenesis is observed in obligate parthenotes, such as lizards in the genus Cnemidophorus and Lacerta, and also in certain facultative parthenotes like the Burmese python.

There appears to be an internal contradiction in the conclusion that "identical duplicate sister chromosomes, produced through premeiotic replication, pair and separate during meiosis I in true parthenotes..... in comparison to the alternative of pairing homologous chromosomes, maintains heterozygosity in obligate parthenotes...." Homologous chromosomal pairings are more likely to create variations.

Half-cloning

Another mechanism typically observed in facultative parthenote reptiles is terminal fusion, in which a haploid polar body produced as a byproduct of normal female meiosis fuses with the egg cell to form a diploid nucleus, much as a haploid sperm cell fuses its nucleus with that of an egg cell to form a diploid genome during sexual reproduction. This method of parthenogenesis produces offspring that are homozygous at nearly all genetic loci, and inherit approximately half of their mother's genetic diversity. This form of parthenogenesis can produce male as well as WW-genotype females. Because the meiosis process proceeds normally in species employing this mechanism, they are capable of both sexual and asexual reproduction, as in the Komodo dragon and several species of snakes.

Types of parthenogenesis

True parthenogenesis

"True" parthenogenesis is a form of asexual reproduction in all-female species that produce offspring without any male involvement.[1]

Lizards

There are at least eight parthenogenetic species of Caucasian rock lizard in the genus Lacerta.[4][5] This genus is unique in containing the only known monoclonal parthenogenetic species, Lacerta rostombekovi, where the entire species originates from a single hybridization event. In all other cases of unisexual reptilian species that have been examined, multiple separate asexual lineages are present.[1] As true parthenotes, Lacerta do not require stimulation from sperm to reproduce.

The best-known and perhaps most evolutionarily derived example of parthenogenesis in reptiles occurs within the Teiid genus of whiptail lizards known as Cnemidophorus. This genus contains at least 13 truly parthenogenetic species, which originate from hybridization events between sexual Cnemidophorus species.[6] Parthenogenetic whiptails are unusual in that they engage in female-female courtship to induce ovulation, with one non-ovulating female engaging in courting behavior normally seen in males while the ovulating female assumes the typical female role. While sex hormone levels in parthenogenetic Cnemidophorus uniparens mimic the cycles seen in their sexual relatives, their nervous systems appear to have evolved unique responses to female sex hormones. Male-like behavior in C. uniparens is correlated with high progesterone levels.[6] This female-female pseudocopulation has also been found to enhance fecundity. A triploid parthenogenetic species in the genus Aspidoscelis, formerly part of Cnemidophorus, has been fertilized with sperm from a sexual species in the same genus to produce a new tetraploid parthenogenetic species in laboratory experiments. Such experiments provide evidence that even truly parthenogenetic species are still capable of incorporating new genetic material and may therefore be capable of evolution.[7]

There are six parthenogenetic gecko species in five genera: Hemidactylus garnotii (Indo-Pacific house gecko), Hemidactylus vietnamensis (Vietnamese house gecko), Hemiphyllodactylus typus (dwarf tree gecko), Heteronotia binoei (Binoe’s gecko), Nactus pelagicus (pelagic gecko), and Lepidodactylus lugubris (mourning gecko). The often quoted parthenogeneetic species N. arnouxi is nomen rejectum (ICZN 1991) and therefore a synonym of N. pelagicus, while Gehyra ogasawarisimae is a misidentified L. lugubris.[8] The gecko Lepidodactylus lugubris is a parthenogenetic species also known to engage in female-female copulation. The species consists of a number of clonal genetic lineages thought to arise from different hybridization events. Surprisingly, parthenogenetic females of this species occasionally produce male offspring, which are thought to be the result of non-genetic hormonal inversions.[9] While these males are anatomically normal, they produce abnormal sperm and are sterile.

Parthenotes are also found in two species of the night lizard genus Lepidophyma. Unlike most parthenogenetic reptiles, Lepidophyma lizards show very low genetic heterozygosity, suggesting a non-hybrid origin.[10]

Snakes

The brahminy blindsnake is a triploid obligate parthenote and the only snake species known to be obligately parthenogenetic.[11]

Facultative parthenogenesis

A juvenile male dragon at the Chester Zoo. Females of the species can occasionally, reproduce through parthenogenesis

Facultative parthenogenesis is the type of parthenogenesis when a female individual can reproduce via both sexual and asexual reproduction.[12] Females can produce viable offspring with or without genetic contribution from a male, and such an ability may, just like true parthenogens, enable colonization of new habitats by single female animals. Facultative parthenogenesis is extremely rare in nature, with only a few examples of animal taxa capable of facultative parthenogenesis, of which none are vertebrate taxa.[12]

Facultative parthenogenesis is often incorrectly used to describe cases of accidental or spontaneous parthenogenesis in normally sexual animals, including many examples in squamata.[13] For example, many cases of accidental parthenogenesis in sharks, some snakes, Komodo dragons and a variety of domesticated birds were widely perpetuated as facultative parthenogenesis.[14] These cases should, however, be considered accidental parthenogenesis, given the frequency of asexually produced eggs and their hatching rates are extremely low, in contrast to true facultative parthenogenesis where the majority of asexually produced eggs hatch.[12][13] In addition, asexually produced offspring in vertebrates exhibit extremely high levels of sterility, highlighting that this mode of reproduction is not adaptive. The occurrence of such asexually produced eggs in sexual animals can be explained by a meiotic error, leading to automictically produced eggs.[13][15]

Gynogenesis

Gynogenesis is a form of asexual reproduction in which female eggs are activated by male sperm, but no male genetic material is contributed to offspring. While this mode of reproduction has not been observed in reptiles, it occurs in several salamander species of the genus Ambystoma.

Hybridogenesis

Hybridogenesis is a variation of parthenogenesis in which males mate with females, but only the mother's genetic material is propagated by these offspring to their own young. While this form of reproduction has not been observed in reptiles, it does occur in frogs of the genus Pelophylax.

Evolution

Origin

In all parthenogenetic reptile species studied to date, chromosomal evidence supports the theory that parthenogenesis arose through a hybridization event, although members of the genus Lepidophyma may be exceptions to this rule.[10][17] The original hybridization event is believed to occur between two related species and is often followed by backcrossing to either parent species to create triploid parthenogenetic offspring. As no crosses of two sexual species in captivity have ever produced parthenogenetic offspring, it is unclear how a hybridization event would actually lead to asexual reproduction. It is possible that parthenogenesis evolved as a way of overcoming sterility due to improper chromosomal pairing and segregation during meiosis in hybrids, and that rare hybrid individuals that could premeiotically duplicate their chromosomes could escape hybrid sterility by reproducing through parthenogenesis. The ability to premeiotically duplicate chromosomes would be selected for in this scenario as it would be the only option for successful reproduction.

Selective advantage

While it is often assumed that parthenogenesis is an inferior evolutionary strategy to sexual reproduction because parthenogenetic species lack the ability to complement genetic mutations through outcrossing or are unable to incorporate new genetic material, research on parthenogenetic species has gradually revealed a number of advantages to this mode of reproduction. Triploid unisexual geckos of the species Heteronotia binoei have greater endurance and aerobic capacity than their diploid ancestors, and this advantage may be the result of polyploidy and a form of hybrid vigor.[18] It has also been observed that obligate parthenotes are often found at high altitudes and in sparse or marginal habitats, a pattern known as "geographical parthenogenesis," and their distribution in suboptimal territories may be a result of their increased colonization ability.[19] A single parthenogenetic individual can colonize a new territory and produce offspring, while for a sexual species multiple individuals would need to occupy a new habitat and come into contact with each other for mating in order for successful colonization to occur. A parthenogenetic species can undergo a more rapid population increase than a sexual species, because all parthenotes are female and produce offspring, while in sexual species half of all individuals are males and do not give birth to offspring. Additionally, laboratory experiments have revealed that even obligate parthenotes retain the capability of incorporating new genetic material through sexual reproduction to form new parthenogenetic lineages, and the ability to outcross on occasion may explain the lengthy evolutionary persistence of some parthenogenetic species.[7]

References

  1. 1 2 3 Macculloch, Ross; Robert Murphy; Larissa Kupriyanova; Ilya Darevsky (January 1997). "The Caucasian rock lizard Lacerta rostombekovi: a monoclonal parthenogenetic vertebrate". Biochemical Systematics and Ecology. 25 (1): 33–37. doi:10.1016/S0305-1978(96)00085-3. Retrieved 19 April 2014.
  2. ↑ Vitt, Laurie J., and Janalee P. Caldwell. Herpetology: an introductory biology of amphibians and reptiles. Academic Press, 2013.
  3. ↑ Lutes, Aracely A.; et al. (2010). "Sister chromosome pairing maintains heterozygosity in parthenogenetic lizards". Nature. 464 (7286): 283–286. doi:10.1038/nature08818.
  4. ↑ Darevskii IS. 1967. Rock lizards of the Caucasus: systematics, ecology and phylogenesis of the polymorphic groups of Caucasian rock lizards of the subgenus Archaeolacerta. Nauka: Leningrad [in Russian: English translation published by the Indian National Scientific Documentation Centre, New Delhi, 1978].
  5. ↑ Tarkhnishvili DN (2012) Evolutionary History, Habitats, Diversification, and Speciation in Caucasian Rock Lizards. In: Advances in Zoology Research, Volume 2 (ed. Jenkins OP), Nova Science Publishers, Hauppauge (NY), p.79-120
  6. 1 2 Moore, Michael C., Joan M. Whittier, and David Crews. "Sex steroid hormones during the ovarian cycle of an all-female, parthenogenetic lizard and their correlation with pseudosexual behavior." General and comparative endocrinology 60.2 (1985): 144-153.
  7. 1 2 Lutes, Aracely A.; et al. (2011). "Laboratory synthesis of an independently reproducing vertebrate species". Proceedings of the National Academy of Sciences. 108 (24): 9910–9915. doi:10.1073/pnas.1102811108.
  8. ↑ Bauer, A.M. (1994). "Familia Gekkonidae (Reptilia, Sauria) Part 1. Australia and Oceania". Das Tierreich. 109: xiii+306.
  9. ↑ Röll, Beate; von Düring, Monika UG (2008). "Sexual characteristics and spermatogenesis in males of the parthenogenetic gecko Lepidodactylus lugubris (Reptilia, Gekkonidae)". Zoology. 111 (5): 385–400. doi:10.1016/j.zool.2007.09.004.
  10. 1 2 Sinclair, Elizabeth A.; et al. (2010). "DNA evidence for nonhybrid origins of parthenogenesis in natural populations of vertebrates". Evolution. 64 (5): 1346–1357.
  11. ↑ Wynn, Addison H., Charles J. Cole, and Alfred L. Gardner. "Apparent triploidy in the unisexual brahminy blind snake, Ramphotyphlops braminus. American Museum novitates; no. 2868." (1987).
  12. 1 2 3 Bell, G. (1982). The Masterpiece of Nature: The Evolution and Genetics of Sexuality, University of California Press, Berkeley, pp. 1- 635 (see page 295). ISBN 0-520-04583-1 ISBN 978-0-520-04583-5
  13. 1 2 3 van der Kooi, C.J.; Schwander, T. (2015). "Parthenogenesis: birth of a new lineage or reproductive accident?" (PDF). Current Biology. 25: R659–R661. doi:10.1016/j.cub.2015.06.055.
  14. ↑ Lampert, K.P. (2008). "Facultative Parthenogenesis in Vertebrates: Reproductive Error or Chance?". Sexual Development. 2 (6): 290–301. PMID 19276631. doi:10.1159/000195678.
  15. ↑ Suomalainen E. et al. (1987). Cytology and Evolution in Parthenogenesis, Boca Raton, CRC Press
  16. ↑ Lowe, Charles H., and John W. Wright. "Evolution of parthenogenetic species of Cnemidophorus (whiptail lizards) in western North America." Journal of the Arizona Academy of Science (1966): 81-87.
  17. ↑ Maslin, T. Paul (1971). "Parthenogenesis in reptiles". American Zoologist. 11 (2): 361–380. doi:10.1093/icb/11.2.361.
  18. ↑ Kearney, Michael; Wahl, Rebecca; Autumn, Kellar (2005). "Increased capacity for sustained locomotion at low temperature in parthenogenetic geckos of hybrid origin". Physiological and Biochemical Zoology. 78 (3): 316–324. doi:10.1086/430033.
  19. ↑ Beukeboom, L. W.; Vrijenhoek, R. C. (1998). "Evolutionary genetics and ecology of sperm‐dependent parthenogenesis". Journal of Evolutionary Biology. 11 (6): 755–782. doi:10.1007/s000360050117.
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