Homology (biology)

The principle of homology: The biological relationships (shown by colors) of the bones in the forelimbs of vertebrates were used by Charles Darwin as an argument in favor of evolution.

In biology, homology is the existence of shared ancestry between a pair of structures, or genes, in different taxa. A common example of homologous structures is the forelimbs of vertebrates, where the wings of bats, the arms of primates, the front flippers of whales and the forelegs of dogs and horses are all derived from the same ancestral tetrapod structure. Evolutionary biology explains homologous structures adapted to different purposes as the result of descent with modification from a common ancestor. Homology was explained by Charles Darwin's theory of evolution in 1859, but had been observed before this, from Aristotle onwards, and it was explicitly analysed by Pierre Belon in 1555. The term was applied to biology by the anatomist Richard Owen in 1843.

In developmental biology, organs that developed in the embryo in the same manner and from similar origins, such as from matching primordia in successive segments of the same animal, are serially homologous. Examples include the legs of a centipede, the maxillary palp and labial palp of an insect, and the spinous processes of successive vertebrae in a vertebral column. Male and female reproductive organs are homologous if they develop from the same embryonic tissue, as do the ovaries and testicles of mammals including humans.

Sequence homology between protein or DNA sequences is similarly defined in terms of shared ancestry. Two segments of DNA can have shared ancestry because of either a speciation event (orthologs) or a duplication event (paralogs). Homology among proteins or DNA is inferred from their sequence similarity. Significant similarity is strong evidence that two sequences are related by divergent evolution from a common ancestor. Alignments of multiple sequences are used to discover the homologous regions.

Homology remains controversial in animal behaviour, but there is suggestive evidence that, for example, dominance hierarchies are homologous across the primates.

History

Pierre Belon compared the skeletons of birds and humans in his Book of Birds (1555).[1]

Homology was noticed by Aristotle (c. 350 BC), and was explicitly analysed by Pierre Belon in his 1555 Book of Birds, where he systematically compared the skeletons of birds and humans. The pattern of similarity was interpreted as part of the static great chain of being through the mediaeval and early modern periods: it was not then seen as implying evolutionary change. In the German Naturphilosophie tradition, homology was of special interest as demonstrating unity in nature.[1][2] In 1790, Goethe stated his foliar theory in his essay "Metamorphosis of Plants", showing that flower part are derived from leaves.[3] The serial homology of limbs was described late in the 18th century. The French zoologist Etienne Geoffroy Saint-Hilaire showed in 1818 in his theorie d'analogue ("theory of homologues") that structures were shared between fishes, reptiles, birds, and mammals. When Geoffroy went further and sought homologies between Georges Cuvier's embranchements, such as vertebrates and molluscs, his claims triggered the 1830 Cuvier-Geoffroy debate. Geoffroy stated the principle of connections, namely that what is important is the relative position of different structures and their connections to each other. The Estonian embryologist Karl Ernst von Baer stated what are now called von Baer's laws in 1828, noting that related animals begin their development as similar embryos and then diverge: thus, animals in the same family are more closely related and diverge later than animals which are only in the same order and have fewer homologies. von Baer's theory recognises that each taxon (such as a family) has distinctive shared features, and that embryonic development parallels the taxonomic hierarchy: not the same as recapitulation theory. The term "homology" was first used in biology by the anatomist Richard Owen in 1843 when studying the similarities of vertebrate fins and limbs, contrasting it with the matching term "analogy" which he used to describe different structures with the same function. In 1859, Charles Darwin explained homologous structures as meaning that the organisms concerned shared a body plan from a common ancestor, and that taxa were branches of a single tree of life.[1][4][2]

Definition

The front wings of beetles such as this five-horned rhinoceros beetle have evolved into elytra, hard wing-cases. These are homologous with the front wings of other insects.

The word homology, coined in about 1656, derives from the Greek ὁμόλογος homologos from ὁμός homos "same" and λόγος logos "relation".[5][6][lower-alpha 1]

The hind wings of Dipteran flies such as this cranefly have evolved divergently to form small club-like halteres. These are homologous with the hind wings of other insects.

Biological structures or sequences in different taxa are homologous if they are derived from a common ancestor. Homology thus implies divergent evolution. For example, many insects (such as dragonflies) possess two pairs of flying wings. In beetles, the first pair of wings has evolved into a pair of hard wing covers,[9] while in Dipteran flies the second pair of wings has evolved into small halteres used for balance.[lower-alpha 2][10]

Similarly, the forelimbs of ancestral vertebrates have evolved into the front flippers of whales, the wings of birds, the running forelegs of dogs, deer, and horses, the short forelegs of frogs and lizards, and the grasping hands of primates including humans. The same major forearm bones (humerus, radius, and ulna[lower-alpha 3]) are found in fossils of lobe-finned fish such as Eusthenopteron.[11]

Homology vs analogy

Sycamore maple fruits have wings analogous to a bird's.

The opposite of homologous organs are analogous organs which do similar jobs in two taxa that were not present in their last common ancestor but rather evolved separately. For example, the wings of insects and birds evolved independently in widely separated groups, and converged functionally to support powered flight, so they are analogous. Similarly, the wings of a sycamore maple seed and the wings of a bird are analogous but not homologous, as they develop from quite different structures.[12][13] A structure can be homologous at one level, but only analogous at another. Pterosaur, bird and bat wings are analogous as wings, but homologous as forelimbs because the organ served as a forearm (not a wing) in the last common ancestor of tetrapods, and evolved in different ways in the three groups. Thus, in the pterosaurs, the "wing" involves both the forelimb and the hindlimb.[14] Analogy is called homoplasy in cladistics, and convergent or parallel evolution in evolutionary biology.[15][16]

In cladistics

Specialised terms are used in taxonomic research. Primary homology is the initial hypothesis made by a researcher based on similar structure or anatomical connections, inferring that two characters share an ancestry. Secondary homology is implied by parsimony analysis, where a character that only occurs once on a tree is taken to be homologous.[17] As implied in this definition, many cladists consider homology to be synonymous with synapomorphy, a shared derived character or trait state that distinguishes a clade from other organisms.[18]

In different taxa

pax6 alterations result in similar changes to eye morphology and function across a wide range of taxa.

Homologies provide the fundamental basis for all biological classification, although some may be highly counter-intuitive. For example, deep homologies like the pax6 genes that control the development of the eyes of vertebrates and arthropods were unexpected, as the organs are anatomically dissimilar and appeared to have evolved entirely independently.[19][20]

In arthropods

The embryonic body segments (somites) of different arthropods taxa have diverged from a simple body plan with many similar appendages which are serially homologous, into a variety of body plans with fewer segments equipped with specialised appendages.[21] The homologies between these have been discovered by comparing genes in evolutionary developmental biology.[19]

Somite
(body
segment)		 Trilobite
(Trilobitomorpha)
 Spider
(Chelicerata)
 Centipede
(Myriapoda)
 Insect
(Hexapoda)
 Shrimp
(Crustacea)
1 antennae chelicerae (jaws and fangs) antennae antennae 1st antennae
2 1st legs pedipalps - - 2nd antennae
3 2nd legs 1st legs mandibles mandibles mandibles (jaws)
4 3rd legs 2nd legs 1st maxillae 1st maxillae 1st maxillae
5 4th legs 3rd legs 2nd maxillae 2nd maxillae 2nd maxillae
6 5th legs 4th legs collum (no legs) 1st legs 1st legs
7 6th legs - 1st legs 2nd legs 2nd legs
8 7th legs - 2nd legs 3rd legs 3rd legs
9 8th legs - 3rd legs - 4th legs
10 9th legs - 4th legs - 5th legs

Among insects, the stinger of the female honey bee is a modified ovipositor, homologous with ovipositors in other insects such as the Orthoptera, Hemiptera, and those Hymenoptera without stingers.[22]

In mammals

The three small bones in the middle ear of mammals including humans, the malleus, incus, and stapes, are today used to transmit sound from the eardrum to the inner ear. The malleus and incus develop in the embryo from structures that form jaw bones (the quadrate and the articular) in lizards, and in fossils of lizard-like ancestors of mammals. Both lines of evidence show that these bones are homologous, sharing a common ancestor.[23]

Among the many homologies in mammal reproductive systems, ovaries and testicles are homologous.[24]

Rudimentary organs such as the human tailbone, now much reduced from their functional state, are readily understood as signs of evolution, the explanation being that they were cut down by natural selection from functioning organs when their functions were no longer needed, but make no sense at all if species are considered to be fixed. The tailbone is homologous to the tails of other primates.[25]

In plants

Leaves, stems, and roots

In many plants, defensive or storage structures are made by modifications of the development of primary leaves, stems, and roots. Leaves are variously modified from photosynthetic structures to form the insect-trapping pitchers of pitcher plants, the insect-trapping jaws of Venus flytrap, and the spines of cactuses, all homologous.[26]

Primary organs Defensive structures Storage structures
Leaves Spines Swollen leaves (e.g. succulents)
Stems Thorns Tubers (e.g. potato), rhizomes (e.g. ginger), fleshy stems (e.g. cacti)
Roots - Root tubers (e.g. sweet potato), taproot (e.g. carrot)

Certain compound leaves of flowering plants are partially homologous both to leaves and shoots, because their development has evolved from a genetic mosaic of leaf and shoot development.[27][28]

Flower parts

The ABC model of flower development. Class A genes affect sepals and petals, class B genes affect petals and stamens, class C genes affect stamens and carpels. In two specific whorls of the floral meristem, each class of organ identity genes is switched on.

The four types of flower parts, namely carpels, stamens, petals, and sepals, are homologous with and derived from leaves, as Goethe correctly noted in 1790. The development of these parts through a pattern of gene expression in the growing zones (meristems) is described by the ABC model of flower development. Each of the four types of flower parts is serially repeated in concentric whorls, controlled by a small number of genes acting in various combinations. Thus, A genes working alone result in sepal formation; A and B together produce petals; B and C together create stamens; C alone produces carpels. When none of the genes are active, leaves are formed. Two more groups of genes, D to form ovules and E for the floral whorls, complete the model. The genes are evidently ancient, as old as the flowering plants themselves.[3]

Developmental biology

The Cretaceous snake Pachyrhachis problematicus had hind legs (circled).

Developmental biology can identify homologous structures that arose from the same tissue in embryogenesis. For example, adult snakes have no legs, but their early embryos have limb-buds for hind legs, which are soon lost as the embryos develop. The implication that the ancestors of snakes had hind legs is confirmed by fossil evidence: the Cretaceous snake Pachyrhachis problematicus had hind legs complete with hip bones (ilium, pubis, ischium), thigh bone (femur), leg bones (tibia, fibula) and foot bones (calcaneum, astragalus) as in tetrapods with legs today.[29]

Sequence homology

A sequence alignment of amino acids for mammalian histone proteins. Sequences conserved across all five species analysed are highlighted in grey. Conservative, semi-conservative, and non-conservative mutations are indicated.[30]

As with anatomical structures, sequence homology between protein or DNA sequences is defined in terms of shared ancestry. Two segments of DNA can have shared ancestry because of either a speciation event (orthologs) or a duplication event (paralogs). Homology among proteins or DNA is typically inferred from their sequence similarity. Significant similarity is strong evidence that two sequences are related by divergent evolution of a common ancestor. Alignments of multiple sequences are used to indicate which regions of each sequence are homologous.[31]

Homologous sequences are orthologous if they are descended from the same ancestral sequence separated by a speciation event: when a species diverges into two separate species, the copies of a single gene in the two resulting species are said to be orthologous. The term "ortholog" was coined in 1970 by the molecular evolutionist Walter Fitch.[32]

Homologous sequences are paralogous if they were created by a duplication event within the genome. For gene duplication events, if a gene in an organism is duplicated to occupy two different positions in the same genome, then the two copies are paralogous. Paralogous genes often belong to the same species. They can shape the structure of whole genomes and thus explain genome evolution to a large extent. Examples include the Homeobox (Hox) genes in animals. These genes not only underwent gene duplications within chromosomes but also whole genome duplications. As a result, Hox genes in most vertebrates are clustered across multiple chromosomes with the HoxA-D clusters being the best studied.[33]

Dominance hierarchy behaviour, as in these weeper capuchin monkeys, may be homologous across the primates.

In behaviour

It has been suggested that some behaviours might be homologous, based on either sharing across related taxa or common origins of the behaviour in an individual's development, though this remains controversial.[34] For example, D. W. Rajecki and Randall C. Flanery, using data on humans and on nonhuman primates, argue that patterns of behaviour in dominance hierarchies are homologous across the primates.[35]

Notes

  1. ↑ The alternative terms "homogeny" and "homogenous" were also used in the late 1800s and early 1900s. However, these terms are now archaic in biology, and the term "homogenous" is now generally found as a misspelling of the term "homogeneous" which refers to the uniformity of a mixture.[7][8]
  2. ↑ If the two pairs of wings are considered as interchangeable, homologous structures, this may be described as a parallel reduction in the number of wings, but otherwise the two changes are each divergent changes in one pair of wings.
  3. ↑ These are coloured in the lead image: humerus brown, radius pale buff, ulna red.

References

  1. 1 2 3 Panchen, A. L. (1999). "Homology—history of a concept". Novartis Found Symp (222): 5–18. PMID 10332750.
  2. 1 2 Brigandt, Ingo (23 November 2011). "Essay: Homology". The Embryo Project Encyclopedia.
  3. 1 2 Dornelas, Marcelo Carnier; Dornelas, Odair (2005). "From leaf to flower: Revisiting Goethe's concepts on the ¨metamorphosis¨ of plants". Brazilian Journal of Plant Physiology. 17 (4). doi:10.1590/S1677-04202005000400001.
  4. ↑ Sommer, R. J. (July 2008). "Homology and the hierarchy of biological systems". Bioessays. 30 (7): 653–658. PMID 18536034. doi:10.1002/bies.20776.
  5. ↑ Bower, Frederick Orpen (1906). "Plant Morphology". Congress of Arts and Science: Universal Exposition, St. Louis, 1904. Houghton, Mifflin. p. 64.
  6. ↑ Williams, David Malcolm; Forey, Peter L. (2004). Milestones in Systematics. CRC Press. p. 198. ISBN 0-415-28032-X.
  7. ↑ "homogeneous, adj.". OED Online. March 2016. Oxford University Press. http://www.oed.com/view/Entry/88045? (accessed April 09, 2016).
  8. ↑ "homogenous, adj.". OED Online. March 2016. Oxford University Press. http://www.oed.com/view/Entry/88055? (accessed April 09, 2016).
  9. ↑ Wagner, Günter P. (2014). Homology, Genes, and Evolutionary Innovation. Princeton University Press. pp. 53–54. ISBN 978-1-4008-5146-1. elytra have very little similarity with typical wings, but are clearly homologous to forewings. Hence butterflies, flies, and beetles all have two pairs of dorsal appendages that are homologous among species.
  10. ↑ Lipshitz, Howard D. (2012). Genes, Development and Cancer: The Life and Work of Edward B. Lewis. Springer. p. 240. ISBN 978-1-4419-8981-9. For example, wing and haltere are homologous, yet widely divergent, organs that normally arise as dorsal appendages of the second thoracic (T2) and third thoracic (T3) segments, respectively.
  11. ↑ "Homology: Legs and Limbs". UC Berkeley. Retrieved 15 December 2016.
  12. ↑ "Secret Found to Flight of 'Helicopter Seeds'". LiveScience. 11 June 2009. Retrieved 2 March 2017.
  13. ↑ Lentink, D.; Dickson, W. B.; van Leeuwen, J. L.; Dickinson, M. H. (12 Jun 2009). "Leading-Edge Vortices Elevate Lift of Autorotating Plant Seeds". Science. 324 (5933): 1438–1440. doi:10.1126/science.1174196.
  14. ↑ Scotland, R. W. (2010). "Deep homology: A view from systematics". BioEssays. 32 (5): 438–449. PMID 20394064. doi:10.1002/bies.200900175.
  15. ↑ Cf. Butler, A. B.: Homology and Homoplasty. In: Squire, Larry R. (Ed.): Encyclopedia of Neuroscience, Academic Press, 2009, pp. 1195–1199.
  16. ↑ "Homologous structure vs. analogous structure: What is the difference?". Retrieved 27 September 2016.
  17. ↑ Pinna, M. C. C. (1991). "Concepts and Tests of Homology in the Cladistic Paradigm". Cladistics. 7 (4): 367–394. doi:10.1111/j.1096-0031.1991.tb00045.x.
  18. ↑ Page, Roderick D.M.; Holmes, Edward C. (2009). Molecular Evolution: A Phylogenetic Approach. John Wiley & Sons. ISBN 978-1-4443-1336-9.
  19. 1 2 Brusca, R.C.; Brusca, G.J. (1990). Invertebrates. Sinauer Associates. p. 669.
  20. ↑ Carroll, Sean B. (2006). Endless Forms Most Beautiful. Weidenfeld & Nicolson. pp. 28, 66–69. ISBN 0-297-85094-6.
  21. ↑ Novartis Foundation; Hall, Brian (2008). Homology. John Wiley. p. 29. ISBN 978-0-470-51566-2.
  22. ↑ Shing, H.; Erickson, E. H. (1982). "Some ultrastructure of the honeybee (Apis mellifera L.) sting". Apidologie. 13 (3): 203–213.
  23. ↑ "Homology: From jaws to ears — an unusual example of a homology". UC Berkeley. Retrieved 15 December 2016.
  24. ↑ Hyde, Janet Shibley; DeLamater, John D. (June 2010), "Chapter 5" (PDF), Understanding Human Sexuality (11th ed.), New York: McGraw-Hill, p. 103, ISBN 978-0-07-338282-1
  25. ↑ Larson 2004, p. 112.
  26. ↑ "Homology: Leave it to the plants". University of California at Berkeley. Retrieved 7 May 2017.
  27. ↑ Sattler R (1984). "Homology — a continuing challenge". Systematic Botany. 9 (4): 382–94. JSTOR 2418787. doi:10.2307/2418787.
  28. ↑ Sattler, R. (1994). "Homology, homeosis, and process morphology in plants". In Hall, Brian Keith. Homology: the hierarchical basis of comparative biology. Academic Press. pp. 423–75. ISBN 0-12-319583-7.
  29. ↑ "Homologies: developmental biology". UC Berkeley. Retrieved 15 December 2016.
  30. ↑ "Clustal FAQ #Symbols". Clustal. Retrieved 8 December 2014.
  31. ↑ Koonin EV (2005). "Orthologs, paralogs, and evolutionary genomics". Annual Review of Genetics. 39: 309–38. PMID 16285863. doi:10.1146/annurev.genet.39.073003.114725.
  32. ↑ Fitch WM (June 1970). "Distinguishing homologous from analogous proteins". Systematic Zoology. 19 (2): 99–113. JSTOR 2412448. PMID 5449325. doi:10.2307/2412448.
  33. ↑ Zakany, Jozsef; Duboule, Denis (2007-08-01). "The role of Hox genes during vertebrate limb development". Current Opinion in Genetics & Development. 17 (4): 359–366. ISSN 0959-437X. PMID 17644373. doi:10.1016/j.gde.2007.05.011.
  34. ↑ Moore, David S (2013). "Importing the homology concept from biology into developmental psychology". Developmental Psychobiology. 55 (1): 13–21. PMID 22711075. doi:10.1002/dev.21015.
  35. ↑ Rajecki, D. W.; Flanery, Randall C. (2013). Lamb, M. E.; Brown, A. L., ed. Social Conflict and Dominance in Children: a Case for a Primate Homology. Advances in Developmental Psychology. Taylor and Francis. p. 125. ISBN 978-1-135-83123-3. Finally, much recent information on children's and nonhuman primates' behavior in groups, a conjunction of hard human data and hard nonhuman primate data, lends credence to our comparison. Our conclusion is that, based on their agreement in several unusual characteristics, dominance patterns are homologous in primates. This agreement of unusual characteristics is found at several levels, including fine motor movement, gross motor movement, and behavior at the group level.

Further reading

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