Abstract
We review the cytological mechanisms underlying asexual reproduction, i.e. reproduction without fertilization, in animals. Asexuality or parthenogenesis has evolved many times and the cytological mechanisms to restore the parental chromosome number can vary between and even within species. In automictic or meiotic parthenogenesis, meiosis takes place but the chromosomal constitution of the mother is restored through one or several different mechanisms. Some of these mechanisms enforce homozygosity at all loci while some other mechanisms pass the genome of the mother intact to the offspring. In apomictic or mitotic parthenogenesis the eggs are formed through what is essentially a set of mitoses. Polyploidy, is in general incompatible with chromosomal sex determination and is a rare condition in animals. However, many asexual and hermaphroditic forms are polyploid to various degrees. Polyploidy is divided into allo- and autopolyploidy. In the former mode the chromosome sets are derived from two or more different species while in autopolyploidy the multiplication has taken place within one species. We discuss the evolutionary consequences of the different cytological mechanisms involved in asexual reproduction.
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References
Asher J Jr (1970) Parthenogenesis and genetic variability. PhD thesis. University of Michigan, Ann Arbor
Asker SE, Jerling L (1992) Apomixis in plants. CRC Press, Boca Raton
Balsano JS, Rasch EM, Monaco PJ (1989) The evolutionary ecology of Poecilia formosa and its triploid associate. In: Meffe GK, Snelson FF (eds) Ecology and evolution of livebearing fishes (Poeciliidae). Prentice Hall, Englewood Cliffs, pp. 277–297
Beukeboom LW, Pijnacker LP (2000) Automictic parthenogenesis in the parasitoid Venturia canescens (Hymeoptera: Ichneumonidae) revisited. Genome 43: 939–944
Bordenstein SR, Werren JH (2007) Bidirectional incompatibility among divergent Wolbachia and incompatibility level differences among closely related Wolbachia in Nasonia. Heredity 99: 278–287
Carroll SB, Grenier JK, Weatherbee SD (2005). From DNA to diversity: molecular genetics and the evolution of animal design. Blackwell, Oxford
Cuellar O (2005) Reproduction and the mechanism of meiotic restitution in the parthenogenetic lizard Cnemidophorus uniparens. J Morphol 133: 139–165
Fountain MT, Hopkin SP (2005) Folsomia candida (Collembola): a “standard” soil arthropod. Annu Rev Ent 50: 201–222
Holloway AK, Cannatella DC, Gerhart HC, Hillis DM (2006) Polyploids with different origins and ancestors from a single sexual polyploid species. Am Nat 167: E88–E101
Hsu WS (1956) Oogenesis in Habrotricha tridens (Milne). Biol Bull 111: 364–374
Lewis WH (ed.) (1980) Polyploidy/biological relevance. Plenum, New York
Lundmark M, Saura A (2006) Asexuality does not explain the success of clonal forms in insects with geographical parthenogenesis. Hereditas 143: 24–33
Ma XF, Gustafson JP (2005) Genome evolution in allopolyploids: a process of cytological and genetic diploidization. Cytogenet Genome Res 109: 236–249
Mark Welch JL, Mark Welch DB, Meselson M (2004) Cytogenetic evidence for asexual evolution of bdelloid rotifers. Proc Natl Acad Sci 101: 1618–1621
Monaco PJ, Rasch EM, Balsano JS (1984) Apomictic reproduction in the Amazon molly, Poecilia formosa, and its triploid hybrids. In: Turner BJ (ed.) Evolutionary genetics of fishes. Plenum Press, New York, pp. 311–328
Narbel-Hofstetter M (1964) Les altérations de la meiose chez les animaux parthénogénétiques. Protoplasmatologia VI. F2. Springer-Verlag, Wien
Norton RA, Kethley JB, Johnston DE, O’Connor BM (1993). Phylogenetic perspectives on genetic systems and reproductive modes of mites. In: Wrensch DL, Ebbert MA (eds) Evolution and diversity of sex ratio in insects and mites. Chapman and Hall, New York, pp. 8–99
Nur U (1979) Gonoid thelytoky in soft scale insects (Coccoidea: Homoptera). Chromosoma 72: 89–104
Pagani M, Ricci R, Redi CA (1993) Oogenesis in Macrotrachela quadricornifera (Rotifera, Bdelloidea). Hydrobiologia 255–256: 225–230
Plantard O, Rasplus J-Y, Mondor G, Le Clainche I, Solignac M (1998) Wolbachia-induced thelytoky in the rose gallwasp Diplolepis spinosissimae (Giraud)(Hymenoptera: Cynipidae), and its consequences on the genetic structure of its host. Proc R Soc Lond B 265: 1075–1090
Saura A, Lokki J, Suomalanen E (1993) Origin of polyploidy in parthenogenetic weevils. J Theor Biol 163: 449–456
Seiler J (1961) Untersuchungen über die Entstehung der Parthenogenese bei Solenobia triquetrella F.R. (Lepidoptera, Psychidae) III. Die geographische Verbreitung der drei Rassen von Solenobia triquetrella (bisexuell, diploid und tetraploid parthenogenetisch) in der Schweiz und in angrenzenden Ländern und die Beziehungen zur Eiszeit. Bemerkungen über die Entstehung der Parthenogenese. Z Vererbungsl 92: 261–316
Seiler J (1963) Untersuchungen über die Entstehung der Parthenogenese bei Solenobia triquetrella F.R. (Lepidoptera, Psychidae). IV. Wie besamen begattete diploid und tetraploid parthenogenetische Weibchen von S. triquetrella ihre Eier? Schicksal der Richtingskörper im unbesamten und besamten Ei. Vergleich der Ergebnisse mit F1-Aufzuchten und Beziehungen zur Genese der Parthenogenese. Z Vererbungsl 94: 29–66
Simonsen V, Holmstrup M (2008). Deviation from apomictic reproduction in Dendrobaena octaedra? Hereditas 145: 212–214
Soltis PS, Soltis DE (2000) The role of genetic and genomic attributes in the success of polyploids. Proc Natl Acad Sci USA 97: 7051–7057
Spitzer B (2006) Local maladaptation in the soft scale insect Saissetia coffeae Hemiptera: Coccidae. Evolution 60: 1859–1867.
Stenberg P, Lundmark M, Knutelski S, Saura A (2003) Evolution of clonality and polyploidy in a weevil system. Mol Biol Evol 20: 1626–1632
Suomalainen E, Saura A, Lokki J (1987) Cytology and evolution in parthenogenesis. CRC Press, Boca Raton
Terhivuo J, Saura A (2006) Dispersal and clonal diversity of North-European parthenogenetic earthworms. Biol Inv 8: 1205–1218
Van Wilgenburg E, Driessen G, Beukeboom LW (2006) Single locus complementary sex determination in Hymenoptera: an “unintelligent” design? Frontiers Zool 3: 1
von Siebold C (1856) Wahre Parthenogenesis bei Schmetterlingen und Bienen. Engelmann, Leipzig
Weeks AR, Braeuwer JAJ (2001) Wolbachia-induced parthenogenesis in a genus of phytophagous mites. Proc R Soc Lond B 268: 2245–2251
White MJD (1946) The evidence against polyploidy in sexually reproducing animals. Am Nat 80: 610–619
White MJD (1970) Heterozygosity and genetic polymorphism in parthenogenetic animals. In: Hecht MK, Steere WC (eds) Essays in evolution and genetics in honour of Theodosus Dobzhansky, suppl. Evol Biol. Appleton-Century-Crofts, New York
White MJD (1973) Animal cytology and evolution, 3rd ed. Cambridge University Press, Cambridge, UK
Zhu HP, Ma DM, Gui JF (2006) Triploid origin of the gibel carp as revealed by 5S rDNA localization and chromosome painting. Chromosome Res 14: 767–776
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Stenberg, P., Saura, A. (2009). Cytology of Asexual Animals. In: Schön, I., Martens, K., Dijk, P. (eds) Lost Sex. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-2770-2_4
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DOI: https://doi.org/10.1007/978-90-481-2770-2_4
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