Homology (biology)

For use of the term 'homologous' in reference to chromosomes, see Homologous chromosomes. For use of the term 'homologous' in reference to behaviors, see Homology (psychology).
The principle of homology: The biological derivation relationship (shown by colors) of the various bones in the forelimbs of four vertebrates is known as homology and was one of Charles Darwin’s arguments in favor of evolution.

In the context of biology, homology is the existence of shared ancestry between a pair of structures, or genes, in different species.[1] A common example of homologous structures in evolutionary biology are the wings of bats and the arms of primates.[1] Evolutionary theory explains the existence of homologous structures adapted to different purposes as the result of descent with modification from a common ancestor.

In the context of sexual differentiation—the process of development of the differences between males and females from an undifferentiated fertilized egg—the male and female organs are homologous if they develop from the same embryonic tissue.[2] A typical example is the ovaries of female humans and the testicles of male humans.[2]

Etymology

The word homology, coined in about 1656, derives from the Greek ὁμόλογος homologos from ὁμός homos "same" and λόγος logos "relation." In biology, two things are homologous if they bear the same relationship to one another, such as a certain bone in various forms of the "hand".

Ray Lankester defined the terms "homogeny", meaning homology due to inheritance from a common ancestor, and "homoplasy", meaning homology due to other factors.[3][4]

Definition

Homology is a relationship defined between structures or DNA derived from a common ancestor. Homologous[Etymology 1] traits of organisms are therefore explained by descent from a common ancestor. The opposite of homologous organs are analogous organs which do similar jobs in two taxa that were not present in the last common ancestor but rather evolved separately. An example of an analogous trait would be the wings of bats and birds, which evolved independently in each lineage separately after diverging from ancestors with forelimbs not used as wings (terrestrial mammals and theropod dinosaurs, respectively).

It is important to distinguish between different hierarchical levels of homology in order to make informative biological comparisons. In the above example, the 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.[5] Homology can also be described at the level of the gene. In genetics homology can refer to both the gene (DNA) and the corresponding protein product. It has been hypothesized that some behaviors might be homologous, based on either shared behavior across related taxa or common origins of the behavior in an individual’s development, though this remains controversial.

Anatomical homology

The wings of pterosaurs (1), bats (2) and birds (3) are analogous as wings, but homologous as forelimbs.

Evolutionary ancestry means that structures evolved from some structure in a common ancestor; for example, the wings of bats and the arms of primates are homologous in this sense. Developmental ancestry means that structures arose from the same tissue in embryonal development; the ovaries of female humans and the testicles of male humans are homologous in this sense.

Homology is different from analogy, which describes the relation between characters that are apparently similar yet phylogenetically independent. The wings of a maple seed and the wings of an albatross are analogous but not homologous (they both allow the organism to travel on the wind, but they didn't both develop from the same structure). Analogy is commonly also referred to as homoplasy, which is further distinguished into parallelism, reversal, and convergence.[6]

From the point of view of evolutionary developmental biology (evo-devo) where evolution is seen as the evolution of the development of organisms, Rolf Sattler emphasized that homology can also be partial. New structures can evolve through the combination of developmental pathways or parts of them. As a result, hybrid or mosaic structures can evolve that exhibit partial homologies. For example, certain compound leaves of flowering plants are partially homologous both to leaves and shoots because they combine some traits of leaves and shoots.[7][8]

Determining homology

Systematists identify two forms of homology: primary homology is that initially conjectured by a researcher based on similar structure or anatomical connections, who states a hypothesis 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.[9] As implied in this definition, many cladists consider homology to be synonymous with synapomorphy.

Homologous structures in other phyla

Introductory discussions of homology commonly limit themselves to the limbs of tetrapod vertebrates, occasionally touching on other structures, such as modified teeth as in whales and elephants. However, homologies provide the fundamental basis for all aspects of biological classification, although some of them may be highly counterintuitive. For example, within the arthropods, Brusca and Brusca [10] provide the following homologies for the first 10 somites (embryonic segments) in several groups of arthropods, but add that "...the subject of head appendage homology among the arthropods is quite unsettled and highly controversial..."

Somite Trilobite Spider
(Chelicerata)		 Centipede
(Uniramia)		 Insect
(Uniramia)		 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

Plants

Modifications of primary leaves, stems, and roots occur in many higher plants.

Examples:

Primary organs Defensive structures Storage structures
Leaves Spines swollen leaves as in succulents
Stems Thorns tubers such as the potato, rhizomes such as ginger, and the fleshy stems of cacti.
Roots - carrot, and root tubers such as sweet potatoes

Sequence homology

A sequence alignment, produced by ClustalO, of mammalian histone proteins.
Sequences are the amino acids for residues 120-180 of the proteins. Residues that are conserved across all sequences are highlighted in grey. Below the protein sequences is a key denoting conserved sequence (*), conservative mutations (:), semi-conservative mutations (.), and non-conservative mutations ( ).[11]

As with anatomical structures, 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).[12]

Homology among proteins or DNA is often incorrectly concluded on the basis of sequence similarity. The terms "percent homology" and "sequence similarity" are often used interchangeably. As with anatomical structures, high sequence similarity might occur because of convergent evolution, or, as with shorter sequences, because of chance. Such sequences are similar but not homologous. Sequence regions that are homologous are also called conserved. This is not to be confused with conservation in amino acid sequences in which the amino acid at a specific position has been substituted with a different one with functionally equivalent physicochemical properties. One can, however, refer to partial homology where a fraction of the sequences compared (are presumed to) share descent, while the rest does not. For example, partial homology may result from a gene fusion event.

Orthology

Homologous sequences are orthologous if they are inferred to be 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. Orthologs, or orthologous genes, are genes in different species that originated by vertical descent from a single gene of the last common ancestor. The term "ortholog" was coined in 1970 by Walter Fitch.[13]

For instance, the plant Flu regulatory protein is present both in Arabidopsis (multicellular higher plant) and Chlamydomonas (single cell green algae). The Chlamydomonas version is more complex: it crosses the membrane twice rather than once, contains additional domains and undergoes alternative splicing. However it can fully substitute the much simpler Arabidopsis protein, if transferred from algae to plant genome by means of gene engineering. Significant sequence similarity and shared functional domains indicate that these two genes are orthologous genes,[14] inherited from the shared ancestor.

Orthology is strictly defined in terms of ancestry. Given that the exact ancestry of genes in different organisms is difficult to ascertain due to gene duplication and genome rearrangement events, the strongest evidence that two similar genes are orthologous is usually found by carrying out phylogenetic analysis of the gene lineage. Orthologs often, but not always, have the same function.[15]

Orthologous sequences provide useful information in taxonomic classification and phylogenetic studies of organisms. The pattern of genetic divergence can be used to trace the relatedness of organisms. Two organisms that are very closely related are likely to display very similar DNA sequences between two orthologs. Conversely, an organism that is further removed evolutionarily from another organism is likely to display a greater divergence in the sequence of the orthologs being studied.

Databases of orthologous genes

Given their tremendous importance for biology and bioinformatics, orthologous genes have been organized in several specializeddatabases that provide tools to identify and analyze orthologous gene sequences. These resources employ approaches that can be generally classified into those that are based on all pairwise sequence comparisons (heuristic) and those that use phylogenetic methods. Sequence comparison methods were first pioneered by COGs,[16] now extended and automatically enhanced by the eggNOG[17] database. InParanoid[18] focuses on pairwise ortholog relationships. OrthoDB[19] appreciates that the orthology concept is relative to different speciation points by providing a hierarchy of orthologs along the species tree. Other databases that provide eukaryotic orthologs include OrthoMCL,[20] OMA, Roundup,[21] OrthoMaM[22] for mammals, OrthologID[23] and GreenPhylDB[24] for plants.

Tree-based phylogenetic approaches aim to distinguish speciation from gene duplication events by comparing gene trees with species trees, as implemented in resources such as TreeFam[25] and LOFT.[26] A third category of hybrid approaches uses both heuristic and phylogenetic methods to construct clusters and determine trees, for example Ortholuge,[27] EnsemblCompara GeneTrees[28] and HomoloGene.[29]

Paralogy

Homologous sequences are paralogous if they were created by a duplication event within the genome. If this was a gene duplication event: 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, but this is not necessary: for example, the hemoglobin gene of humans and the myoglobin gene of chimpanzees are paralogs. Paralogs can be split into in-paralogs (paralogous pairs that arose after a speciation event) and out-paralogs (paralogous pairs that arose before a speciation event). Between-species out-paralogs are pairs of paralogs that exist between two organisms due to duplication before speciation, whereas within-species out-paralogs are pairs of paralogs that exist in the same organism, but whose duplication event happened before speciation. Paralogs typically have the same or similar function, but sometimes do not: due to lack of the original selective pressure upon one copy of the duplicated gene, this copy is free to mutate and acquire new functions.

Paralogous sequences provide useful and dramatic insight into some of the way genomes evolve. The genes encoding myoglobin and hemoglobin are considered to be ancient paralogs. Similarly, the four known classes of hemoglobins (hemoglobin A, hemoglobin A2, hemoglobin B, and hemoglobin F) are paralogs of each other. While each of these proteins serves the same basic function of oxygen transport, they have already diverged slightly in function: fetal hemoglobin (hemoglobin F) has a higher affinity for oxygen than adult hemoglobin. Function is not always conserved, however. Human angiogenin diverged from ribonuclease, for example, and while the two paralogs remain similar in tertiary structure, their functions within the cell are now quite different.

It is often asserted that orthologs are more functionally similar than paralogs of similar divergence, but several papers have challenged this notion.[30][31][32]

Ohnology

Ohnologous genes are paralogous genes that have originated by a process of whole-genome duplication (WGD). The name was first given in honour of Susumu Ohno by Ken Wolfe.[33] Ohnologs/Ohnologues are interesting for evolutionary analysis because they all have been diverging for the same length of time since their common origin.

Xenology

Homologs resulting from horizontal gene transfer between two organisms are termed xenologs. Xenologs can have different functions, if the new environment is vastly different for the horizontally moving gene. In general, though, xenologs typically have similar function in both organisms. The term was coined by Walter Fitch.[13]

Gametology

Gametology denotes the relationship between homologous genes on nonrecombining, opposite sex chromosomes. Gametologs result from the origination of genetic sex determination and barriers to recombination between sex chromosomes. Examples of gametologs include CHDW and CHDZ in birds.

Homology between sexes and forms

The term homology is sometimes applied to reproductive structures that share a common embryonic origin, but become spectacularly different between the two sexes in the adult. Those listed below are some of the more commonly cited examples.

Male structure Female structure Notes
prostate skene's gland -
penis clitoris -
- uterus homologous to eggshell-depositing organs in reptiles and birds
bulbourethral gland Bartholin's gland -

Among insects, the stinger used by infertile female worker bees is a modified ovipositor.

Homologies across phyla

For more details on this topic, see Deep homology.

See also

Notes

  1. ↑ from Greek ομολογειν, 'to agree'

    References

    1. ↑ 1.0 1.1 "Homology". Encyclopædia Britannica Online. Retrieved 2013-08-30.
    2. ↑ 2.0 2.1 Hyde, Janet Shibley; DeLamater, John D. (June 2010), "Chapter 5", Understanding Human Sexuality (11th ed.), New York: McGraw-Hill, p. 103, ISBN 978-0073382821
    3. ↑ Bower, Frederick Orpen (1906). "Plant Morphology". Congress of Arts and Science: Universal Exposition, St. Louis, 1904. Houghton, Mifflin. p. 64.
    4. ↑ Williams, David Malcolm; Forey, Peter L. (2004). Milestones in Systematics. CRC Press. p. 198. ISBN 0-415-28032-X.
    5. ↑ Scotland, R. W. (2010). "Deep homology: A view from systematics". BioEssays 32 (5): 438–449. doi:10.1002/bies.200900175. PMID 20394064.
    6. ↑ Cf. Butler, A. B.: Homology and Homoplasty. In: Squire, Larry R. (Ed.): Encyclopedia of Neuroscience, Academic Press, 2009, pp. 1195–1199.
    7. ↑ Sattler R (1984). "Homology — a continuing challenge". Systematic Botany 9 (4): 382–94. doi:10.2307/2418787. JSTOR 2418787.
    8. ↑ 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.
    9. ↑ 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.
    10. ↑ Brusca, R.C. & Brusca, G.J. 1990. Invertebrates. Sinauer Associates, Sunderland.: [i]-xviii, 1-922., P. 669
    11. ↑ "Clustal FAQ #Symbols". Clustal. Retrieved 8 December 2014.
    12. ↑ Koonin EV (2005). "Orthologs, paralogs, and evolutionary genomics". Annual Review of Genetics 39: 309–38. doi:10.1146/annurev.genet.39.073003.114725. PMID 16285863.
    13. ↑ 13.0 13.1 Fitch WM (June 1970). "Distinguishing homologous from analogous proteins". Systematic Zoology 19 (2): 99–113. doi:10.2307/2412448. PMID 5449325.
    14. ↑ Falciatore A, Merendino L, Barneche F et al. (January 2005). "The FLP proteins act as regulators of chlorophyll synthesis in response to light and plastid signals in Chlamydomonas". Genes & Development 19 (1): 176–87. doi:10.1101/gad.321305. PMC 540235. PMID 15630026.
    15. ↑ Fang G, Bhardwaj N, Robilotto R, Gerstein MB (March 2010). "Getting started in gene orthology and functional analysis". PLoS Computational Biology 6 (3): e1000703. doi:10.1371/journal.pcbi.1000703. PMC 2845645. PMID 20361041.
    16. ↑ COGs: Clusters of Orthologous Groups of proteins
      Tatusov RL, Koonin EV, Lipman DJ (October 1997). "A genomic perspective on protein families". Science 278 (5338): 631–7. doi:10.1126/science.278.5338.631. PMID 9381173.
    17. ↑ eggNOG: evolutionary genealogy of genes: Non-supervised Orthologous Groups
      Muller J, Szklarczyk D, Julien P et al. (January 2010). "eggNOG v2.0: extending the evolutionary genealogy of genes with enhanced non-supervised orthologous groups, species and functional annotations". Nucleic Acids Research 38 (Database issue): D190–5. doi:10.1093/nar/gkp951. PMC 2808932. PMID 19900971.
    18. ↑ Inparanoid: Eukaryotic Ortholog Groups
      Ostlund G, Schmitt T, Forslund K et al. (January 2010). "InParanoid 7: new algorithms and tools for eukaryotic orthology analysis". Nucleic Acids Research 38 (Database issue): D196–203. doi:10.1093/nar/gkp931. PMC 2808972. PMID 19892828.
    19. ↑ OrthoDB: The Hierarchical Catalog of Eukaryotic Orthologs
      Waterhouse RM, Zdobnov EM, Tegenfeldt F, Li J, Kriventseva EV (January 2011). "OrthoDB: the hierarchical catalog of eukaryotic orthologs in 2011". Nucleic Acids Research 39 (Database issue): D283–8. doi:10.1093/nar/gkq930. PMC 3013786. PMID 20972218.
    20. ↑ OrthoMCL: Identification of Ortholog Groups for Eukaryotic Genomes
      Chen F, Mackey AJ, Stoeckert CJ, Roos DS (January 2006). "OrthoMCL-DB: querying a comprehensive multi-species collection of ortholog groups". Nucleic Acids Research 34 (Database issue): D363–8. doi:10.1093/nar/gkj123. PMC 1347485. PMID 16381887.
    21. ↑ Roundup
      Deluca TF, Wu IH, Pu J et al. (August 2006). "Roundup: a multi-genome repository of orthologs and evolutionary distances". Bioinformatics (Oxford, England) 22 (16): 2044–6. doi:10.1093/bioinformatics/btl286. PMID 16777906.
    22. ↑ OrthoMaM
      Ranwez V, Delsuc F, Ranwez S, Belkhir K, Tilak MK, Douzery EJ (2007). "OrthoMaM: a database of orthologous genomic markers for placental mammal phylogenetics". BMC Evolutionary Biology 7: 241. doi:10.1186/1471-2148-7-241. PMC 2249597. PMID 18053139.
    23. ↑ OrthologID
      Chiu JC, Lee EK, Egan MG, Sarkar IN, Coruzzi GM, DeSalle R (March 2006). "OrthologID: automation of genome-scale ortholog identification within a parsimony framework". Bioinformatics 22 (6): 699–707. doi:10.1093/bioinformatics/btk040. PMID 16410324.
    24. ↑ GreenPhylDB
      Conte MG, Gaillard S, Lanau N, Rouard M, Périn C (January 2008). "GreenPhylDB: a database for plant comparative genomics". Nucleic Acids Research 36 (Database issue): D991–8. doi:10.1093/nar/gkm934. PMC 2238940. PMID 17986457.
    25. ↑ TreeFam: Tree families database
      Ruan J, Li H, Chen Z et al. (January 2008). "TreeFam: 2008 Update". Nucleic Acids Research 36 (Database issue): D735–40. doi:10.1093/nar/gkm1005. PMC 2238856. PMID 18056084.
    26. ↑ TreeFam: Tree families database
      van der Heijden RT, Snel B, van Noort V, Huynen MA (2007). "Orthology prediction at scalable resolution by phylogenetic tree analysis". BMC Bioinformatics 8: 83. doi:10.1186/1471-2105-8-83. PMC 1838432. PMID 17346331.
    27. ↑ Fulton DL, Li YY, Laird MR, Horsman BG, Roche FM, Brinkman FS (2006). "Improving the specificity of high-throughput ortholog prediction". BMC Bioinformatics 7: 270. doi:10.1186/1471-2105-7-270. PMC 1524997. PMID 16729895.
    28. ↑ Vilella AJ, Severin J, Ureta-Vidal A, Heng L, Durbin R, Birney E (February 2009). "EnsemblCompara GeneTrees: Complete, duplication-aware phylogenetic trees in vertebrates". Genome Research 19 (2): 327–35. doi:10.1101/gr.073585.107. PMC 2652215. PMID 19029536.
    29. ↑ Sayers EW, Barrett T, Benson DA et al. (January 2011). "Database resources of the National Center for Biotechnology Information". Nucleic Acids Research 39 (Database issue): D38–51. doi:10.1093/nar/gkq1172. PMC 3013733. PMID 21097890.
    30. ↑ Studer RA, Robinson-Rechavi M (May 2009). "How confident can we be that orthologs are similar, but paralogs differ?". Trends in Genetics 25 (5): 210–6. doi:10.1016/j.tig.2009.03.004. PMID 19368988.
    31. ↑ Nehrt NL, Clark WT, Radivojac P, Hahn MW (June 2011). "Testing the ortholog conjecture with comparative functional genomic data from mammals". PLoS Computational Biology 7 (6): e1002073. doi:10.1371/journal.pcbi.1002073. PMC 3111532. PMID 21695233.
    32. ↑ Eisen, Jonathan. "Special Guest Post & Discussion Invitation from Matthew Hahn on Ortholog Conjecture Paper".
    33. ↑ Wolfe K (May 2000). "Robustness--it's not where you think it is". Nature Genetics 25 (1): 3–4. doi:10.1038/75560. PMID 10802639.

    Further reading

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