Mating system

A mating system is a way in which a group is structured in relation to sexual behaviour. The precise meaning depends upon the context. With respect to animals, the term describes which males and females mate, under which circumstances; recognised systems include monogamy, polygamy (which includes polygyny, polyandry, and polygynandry), and promiscuity, all of which lead to different mate choice outcomes and thus these systems affect how sexual selection works in the species which practice them. In plants, the term refers to the degree and circumstances of outcrossing. In human sociobiology, the terms have been extended to encompass the formation of relationships such as marriage.

In plants

The primary mating systems in plants are outcrossing (cross-fertilisation), autogamy (self-fertilisation) and apomixis (asexual reproduction without fertilization, but only when arising by modification of sexual function). Mixed mating systems, in which plants use two or even all three mating systems, are not uncommon.[1]

A number of models have been used to describe the parameters of plant mating systems. The basic model is the mixed mating model, which is based on the assumption that every fertilisation is either self-fertilisation or completely random cross-fertilisation. More complex models relax this assumption; for example, the effective selfing model recognises that mating may be more common between pairs of closely related plants than between pairs of distantly related plants.[1]

In animals

Chimpanzees have a promiscuous mating system
Male and female gorilla, gorillas have a polygynous mating system

The following are some of the mating systems generally recognized in animals:

These mating relationships may or may not be associated with social relationships, in which the sexual partners stay together to become parenting partners. As the alternative term "pair bonding" implies, this is usual in monogamy. In many polyandrous systems, the males and the female stay together to rear the young. In polygynous systems where the number of females paired with each male is low and the male will often stay with one female to help rear the young, while the other females rear their young on their own. In polygynandry, each of the males may assist one female; if all adults help rear all the young, the system is more usually called "communal breeding". In highly polygynous systems, and in promiscuous systems, paternal care of young is rare, or there may be no parental care at all.

These descriptions are idealized, and the social partnerships are often easier to observe than the mating relationships. In particular:

In humans

Compared to other vertebrates, where a species usually has a single mating system, human display great variety. Humans also differ by having formal marriages which in many cultures involve negotiation and arrangement between elder relatives. Regarding sexual dimorphism (see the section about animals above), humans are in the intermediate group with moderate sex differences in body size but with relatively large testes. This indicates relatively frequent sperm competition which is supported by reports of extrapair paternity of 2-22% in socially monogamous and polygynous human societies. One estimate is that 83% of human societies are polygynous, 0.05% are polyandrous, and the rest are monogamous. Even the last group may at least in part be genetically polygynous.[4]

Polygyny is associated with an increased sharing of subsistence provided by women. This is consistent with the theory that if women raise the children alone, men can concentrate on the mating effort. Polygyny is also associated with greater environmental variability in the form of variability of rainfall. This may increase the differences in the resources available to men. An important association is that polygyny is associated with a higher pathogen load in an area which may make having good genes in a male increasingly important. A high pathogen load also decreases the relative importance of sororal polygyny which may be because it becomes increasingly important to have genetic variability in the offspring (See Major histocompatibility complex and sexual selection).[4]

Virtually all the terms used to describe animal mating systems were adopted from social anthropology, where they had been devised to describe systems of marriage. This shows that human sexual behavior is unusually flexible since, in most animal species, one mating system dominates. While there are close analogies between animal mating systems and human marriage institutions, these analogies should not be pressed too far, because in human societies, marriages typically have to be recognized by the entire social group in some way, and there is no equivalent process in animal societies. The temptation to draw conclusions about what is "natural" for human sexual behavior from observations of animal mating systems should be resisted: a socio-biologist observing the kinds of behavior shown by humans in any other species would conclude that all known mating systems were natural for that species, depending on the circumstances or on individual differences.

As culture increasingly affects human mating choices, ascertaining what is the 'natural' mating system of the human animal from a zoological perspective becomes increasingly difficult. Some clues can be taken from human anatomy, which is essentially unchanged from the prehistoric past:

Some have suggested that these anatomical factors signify some degree of sperm competition, though as levels of genetic and societal promiscuity are highly varied across cultures,[5] this evidence is far from conclusive.

In microorganisms

Bacteria

Mating in bacteria involves transfer of DNA from one cell to another and incorporation of the transferred DNA into the recipient bacteria’s genome by homologous recombination. Transfer of DNA between bacterial cells can occur in three main ways. First, a bacterium can take up exogenous DNA released into the intervening medium from another bacterium by a process called transformation. DNA can also be transferred from one bacterium to another by the process of transduction, which is mediated by an infecting virus (bacteriophage). The third method of DNA transfer is conjugation, in which a plasmid mediates transfer through direct cell contact between cells.

Transformation, unlike transduction or conjugation, depends on numerous bacterial gene products that specifically interact to perform this complex process,[6] and thus transformation is clearly a bacterial adaptation for DNA transfer. In order for a bacterium to bind, take up and recombine donor DNA into its own chromosome, it must first enter a special physiological state termed natural competence. In Bacillus subtilis about 40 genes are required for the development of competence and DNA uptake.[7] The length of DNA transferred during B. subtilis transformation can be as much as a third and up to the whole chromosome.[8][9] Transformation appears to be common among bacterial species, and at least 60 species are known to have the natural ability to become competent for transformation.[10] The development of competence in nature is usually associated with stressful environmental conditions, and seems to be an adaptation for facilitating repair of DNA damage in recipient cells.[11]

Archaea

In several species of archaea, mating is mediated by formation of cellular aggregates. Halobacterium volcanii, an extreme halophilic archaeon, forms cytoplasmic bridges between cells that appear to be used for transfer of DNA from one cell to another in either direction.[12]

When the hyperthermophilic archaea Sulfolobus solfataricus[13] and Sulfolobus acidocaldarius[14] are exposed to the DNA damaging agents UV irradiation, bleomycin or mitomycin C, species-specific cellular aggregation is induced. Aggregation in S. solfataricus could not be induced by other physical stressors, such as pH or temperature shift,[13] suggesting that aggregation is induced specifically by DNA damage. Ajon et al.[14] showed that UV-induced cellular aggregation mediates chromosomal marker exchange with high frequency in S. acidocaldarius. Recombination rates exceeded those of uninduced cultures by up to three orders of magnitude. Frols et al.[13] and Ajon et al.[14] hypothesized that cellular aggregation enhances species-specific DNA transfer between Sulfolobus cells in order to provide increased repair of damaged DNA by means of homologous recombination. This response appears to be a primitive form of sexual interaction similar to the more well-studied bacterial transformation systems that are also associated with species specific DNA transfer between cells leading to homologous recombinational repair of DNA damage.[15]

Protists

Protists are a large group of diverse eukaryotic microorganisms, mainly unicellular animals and plants, that do not form tissues. Eukaryotes emerged in evolution more than 1.5 billion years ago.[16] The earliest eukaryotes were likely protists. Mating and sexual reproduction are widespread among extant eukaryotes. Based on a phylogenetic analysis, Dacks and Roger[17] proposed that facultative sex was present in the common ancestor of all eukaryotes.

However, to many biologists it seemed unlikely until recently, that mating and sex could be a primordial and fundamental characteristic of eukaryotes. A principal reason for this view was that mating and sex appeared to be lacking in certain pathogenic protists whose ancestors branched off early from the eukaryotic family tree. However, several of these protists are now known to be capable of, or to recently have had, the capability for meiosis and hence mating. To cite one example, the common intestinal parasite Giardia intestinalis was once considered to be a descendant of a protist lineage that predated the emergence of meiosis and sex. However, G. intestinalis was recently found to have a core set of genes that function in meiosis and that are widely present among sexual eukaryotes.[18] These results suggested that G. intestinalis is capable of meiosis and thus mating and sexual reproduction. Furthermore, direct evidence for meiotic recombination, indicative of mating and sexual reproduction, was also found in G. intestinalis.[19][19] Other protists for which evidence of mating and sexual reproduction has recently been described are parasitic protozoa of the genus Leishmania,[20] Trichomonas vaginalis,[21] and acanthamoeba.[22]

Protists generally reproduce asexually under favorable environmental conditions, but tend to reproduce sexually under stressful conditions, such as starvation or heat shock.[15]

Viruses

Both animal viruses and bacterial viruses (bacteriophage) are able to undergo mating. When a cell is mixedly infected by two genetically marked viruses, recombinant virus progeny are often observed indicating that mating interaction had occurred at the DNA level. Another manifestation of mating between viral genomes is multiplicity reactivation (MR). MR is the process by which at least two virus genomes, each containing inactivating genome damage, interact with each other in an infected cell to form viable progeny viruses. The genes required for MR in bacteriophage T4 are largely the same as the genes required for allelic recombination.[23] Examples of MR in animal viruses are described in the articles Herpes simplex virus, Influenza A virus, Adenoviridae, Simian virus 40, Vaccinia virus, and Reoviridae.

See also

References

  1. 1 2 Brown, A. H. D.; et al. (1989). "Isozyme analysis of plant mating systems". In Soltis, D. E.; Soltis, P. S. Isozymes in Plant Biology. Portland: Dioscorides Press. pp. 73–86.
  2. ↑ Pickett, K. M., Osborne, D. M., Wahl, D., and Wenzel, J. W. (2001). "An Enormous Nest of Vespula squamosa from Florida, the Largest Social Was Nest Reported from North America, with Notes on Colony Cycle and Reproduction", "Journal of the New York Entomological Society", 2001.
  3. ↑ McAuslane, H. J.; Vinson, S. B.; Williams, H. J. (1990-06-01). "Change in mandibular and mesosomal gland contents of maleXylocopa micans (Hymenoptera: Anthophoridae) associated with mating system". Journal of Chemical Ecology. 16 (6): 1877–1885. doi:10.1007/BF01020501. ISSN 0098-0331.
  4. 1 2 The Oxford Handbook of Evolutionary Psychology, Edited by Robin Dunbar and Louise Barret, Oxford University Press, 2007, Chapter 30 Ecological and socio-cultural impacts on mating and marriage systems by Bobbi S. Low
  5. ↑ http://raptor1.bizlab.mtsu.edu/s-drive/TEFF/662/papers2010/men_dominance/The%20Mating%20System%20of%20Foragers%20in%20the%20Standard%20Cross-Cultural%20Sample.pdf
  6. ↑ Chen I, Dubnau D (2004). "DNA uptake during bacterial transformation". Nat. Rev. Microbiol. 2 (3): 241–9. doi:10.1038/nrmicro844. PMID 15083159.
  7. ↑ Solomon JM, Grossman AD (1996). "Who's competent and when: regulation of natural genetic competence in bacteria". Trends Genet. 12 (4): 150–5. doi:10.1016/0168-9525(96)10014-7. PMID 8901420.
  8. ↑ Akamatsu T, Taguchi H (2001). "Incorporation of the whole chromosomal DNA in protoplast lysates into competent cells of Bacillus subtilis". Biosci. Biotechnol. Biochem. 65 (4): 823–9. doi:10.1271/bbb.65.823. PMID 11388459.
  9. ↑ Saito Y, Taguchi H, Akamatsu T (2006). "Fate of transforming bacterial genome following incorporation into competent cells of Bacillus subtilis: a continuous length of incorporated DNA". J. Biosci. Bioeng. 101 (3): 257–62. doi:10.1263/jbb.101.257. PMID 16716928.
  10. ↑ Johnsborg O, Eldholm V, Håvarstein LS (2007). "Natural genetic transformation: prevalence, mechanisms and function". Res. Microbiol. 158 (10): 767–78. doi:10.1016/j.resmic.2007.09.004. PMID 17997281.
  11. ↑ Bernstein H, Bernstein C, Michod RE (2012). DNA repair as the primary adaptive function of sex in bacteria and eukaryotes. Chapter 1: pp.1-49 in: DNA Repair: New Research, Sakura Kimura and Sora Shimizu editors. Nova Sci. Publ., Hauppauge, N.Y. ISBN 978-1-62100-808-8 https://www.novapublishers.com/catalog/product_info.php?products_id=31918
  12. ↑ Rosenshine I, Tchelet R, Mevarech M (1989). "The mechanism of DNA transfer in the mating system of an archaebacterium". Science. 245 (4924): 1387–9. doi:10.1126/science.2818746. PMID 2818746.
  13. 1 2 3 Fröls S, Ajon M, Wagner M, Teichmann D, Zolghadr B, Folea M, Boekema EJ, Driessen AJ, Schleper C, Albers SV (2008). "UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation". Mol. Microbiol. 70 (4): 938–52. doi:10.1111/j.1365-2958.2008.06459.x. PMID 18990182.
  14. 1 2 3 Ajon M, Fröls S, van Wolferen M, Stoecker K, Teichmann D, Driessen AJ, Grogan DW, Albers SV, Schleper C (2011). "UV-inducible DNA exchange in hyperthermophilic archaea mediated by type IV pili". Mol. Microbiol. 82 (4): 807–17. doi:10.1111/j.1365-2958.2011.07861.x. PMID 21999488.
  15. 1 2 Bernstein H and Bernstein C (2013). Evolutionary Origin and Adaptive Function of Meiosis. In Meiosis: Bernstein C and Bernstein H, editors. ISBN 978-953-51-1197-9, InTech, http://www.intechopen.com/books/meiosis/evolutionary-origin-and-adaptive-function-of-meiosis
  16. ↑ Javaux EJ, Knoll AH, Walter MR (2001). "Morphological and ecological complexity in early eukaryotic ecosystems". Nature. 412 (6842): 66–9. doi:10.1038/35083562. PMID 11452306.
  17. ↑ Dacks J, Roger AJ (1999). "The first sexual lineage and the relevance of facultative sex". J. Mol. Evol. 48 (6): 779–83. doi:10.1007/pl00013156. PMID 10229582.
  18. ↑ Ramesh MA, Malik SB, Logsdon JM (2005). "A phylogenomic inventory of meiotic genes; evidence for sex in Giardia and an early eukaryotic origin of meiosis". Curr. Biol. 15 (2): 185–91. doi:10.1016/j.cub.2005.01.003. PMID 15668177.
  19. 1 2 Cooper MA, Adam RD, Worobey M, Sterling CR (2007). "Population genetics provides evidence for recombination in Giardia". Curr. Biol. 17 (22): 1984–8. doi:10.1016/j.cub.2007.10.020. PMID 17980591.
  20. ↑ Akopyants NS, Kimblin N, Secundino N, Patrick R, Peters N, Lawyer P, Dobson DE, Beverley SM, Sacks DL (2009). "Demonstration of genetic exchange during cyclical development of Leishmania in the sand fly vector". Science. 324 (5924): 265–8. doi:10.1126/science.1169464. PMC 2729066Freely accessible. PMID 19359589.
  21. ↑ Malik SB, Pightling AW, Stefaniak LM, Schurko AM, Logsdon JM (2008). "An expanded inventory of conserved meiotic genes provides evidence for sex in Trichomonas vaginalis". PLoS ONE. 3 (8): e2879. doi:10.1371/journal.pone.0002879. PMC 2488364Freely accessible. PMID 18663385.
  22. ↑ Khan NA, Siddiqui R (2015). "Is there evidence of sexual reproduction (meiosis) in Acanthamoeba?". Pathog Glob Health. 109 (4): 193–5. doi:10.1179/2047773215Y.0000000009. PMID 25800982.
  23. ↑ Bernstein C (1981). "Deoxyribonucleic acid repair in bacteriophage". Microbiol. Rev. 45 (1): 72–98. PMC 281499Freely accessible. PMID 6261109.

Further reading

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