Common descent

Common descent is a concept in evolutionary biology applicable when one species is the ancestor of two or more species later in time. Its broadest application, the last universal common ancestor (LUCA) of all life on Earth, is a central assumption of modern evolutionary theory.[1][2]

Common descent is an effect of speciation, in which multiple species derive from a single ancestral population. The more recent the ancestral population two species have in common, the more closely are they related. The most recent common ancestor of all currently living organisms is the last universal ancestor,[1] which lived about 3.9 billion years ago.[3][4] The two earliest pieces of evidence for life on Earth are graphite found to be biogenic in 3.7 billion-year-old metasedimentary rocks discovered in western Greenland[5] and microbial mat fossils found in 3.48 billion-year-old sandstone discovered in Western Australia.[6][7] All currently living organisms on Earth share a common genetic heritage, though the suggestion of substantial horizontal gene transfer during early evolution has led to questions about the monophyly (single ancestry) of life.[1] 6,331 groups of genes common to all living animals have been identified; these may have arisen from a single common ancestor that lived 650 million years ago in the Precambrian.[8][9]

Universal common descent through an evolutionary process was first proposed by the British naturalist Charles Darwin in the concluding sentence of his 1859 book On the Origin of Species:

There is grandeur in this view of life, with its several powers, having been originally breathed into a few forms or into one; and that, whilst this planet has gone cycling on according to the fixed law of gravity, from so simple a beginning endless forms most beautiful and most wonderful have been, and are being, evolved.[10]

History

In the 1740s, the French mathematician Pierre Louis Maupertuis made the first known suggestion that all organisms had a common ancestor, and had diverged through random variation and natural selection.[11][12] In Essai de cosmologie (1750), Maupertuis noted:

May we not say that, in the fortuitous combination of the productions of Nature, since only those creatures could survive in whose organizations a certain degree of adaptation was present, there is nothing extraordinary in the fact that such adaptation is actually found in all these species which now exist? Chance, one might say, turned out a vast number of individuals; a small proportion of these were organized in such a manner that the animals' organs could satisfy their needs. A much greater number showed neither adaptation nor order; these last have all perished.... Thus the species which we see today are but a small part of all those that a blind destiny has produced.[13]

In 1790, the philosopher Immanuel Kant wrote in Kritik der Urteilskraft (Critique of Judgment) that the similarity[lower-alpha 1] of animal forms implies a common original type, and thus a common parent.[14]

In 1794, Charles Darwin's grandfather, Erasmus Darwin asked:

[W]ould it be too bold to imagine, that in the great length of time, since the earth began to exist, perhaps millions of ages before the commencement of the history of mankind, would it be too bold to imagine, that all warm-blooded animals have arisen from one living filament, which the great First Cause endued with animality, with the power of acquiring new parts attended with new propensities, directed by irritations, sensations, volitions, and associations; and thus possessing the faculty of continuing to improve by its own inherent activity, and of delivering down those improvements by generation to its posterity, world without end?[15]

Charles Darwin's views about common descent, as expressed in On the Origin of Species, were that it was probable that there was only one progenitor for all life forms:

Therefore I should infer from analogy that probably all the organic beings which have ever lived on this earth have descended from some one primordial form, into which life was first breathed.[16]

But he precedes that remark by, "Analogy would lead me one step further, namely, to the belief that all animals and plants have descended from some one prototype. But analogy may be a deceitful guide." And in the subsequent edition,[17] he asserts rather,

"We do not know all the possible transitional gradations between the simplest and the most perfect organs; it cannot be pretended that we know all the varied means of Distribution during the long lapse of years, or that we know how imperfect the Geological Record is. Grave as these several difficulties are, in my judgment they do not overthrow the theory of descent from a few created forms with subsequent modification".

Common descent was widely accepted amongst the scientific community after Darwin's publication.[18] In 1907, Vernon Kellogg commented that "practically no naturalists of position and recognized attainment doubt the theory of descent."[19]

In 2008, biologist T. Ryan Gregory noted that:

No reliable observation has ever been found to contradict the general notion of common descent. It should come as no surprise, then, that the scientific community at large has accepted evolutionary descent as a historical reality since Darwin’s time and considers it among the most reliably established and fundamentally important facts in all of science.[20]

Evidence

Common biochemistry

All known forms of life are based on the same fundamental biochemical organization: genetic information encoded in DNA, transcribed into RNA, through the effect of protein- and RNA-enzymes, then translated into proteins by (highly similar) ribosomes, with ATP, NADPH and others as energy sources. Analysis of small sequence differences in widely shared substances such as cytochrome c further supports universal common descent.[21] Some 23 proteins are found in all organisms, serving as enzymes carrying out core functions like DNA replication. The fact that only one such set of enzymes exists is convincing evidence of a single ancestry.[1][22] 6,331 genes common to all living animals have been identified; these may have arisen from a single common ancestor that lived 650 million years ago in the Precambrian.[8][9]

Common genetic code

Amino acids nonpolar polar basic acidic Stop codon
Standard genetic code
1st
base
2nd base
T C A G
T TTT Phenyl-
alanine
TCT Serine TAT Tyrosine TGT Cysteine
TTC TCC TAC TGC
TTA Leucine TCA TAA Stop TGA Stop
TTG TCG TAG Stop TGG Tryptophan 
C CTT CCT Proline CAT Histidine CGT Arginine
CTC CCC CAC CGC
CTA CCA CAA Glutamine CGA
CTG CCG CAG CGG
A ATT Isoleucine ACT Threonine  AAT Asparagine AGT Serine
ATC ACC AAC AGC
ATA ACA AAA Lysine AGA Arginine
ATG Methionine ACG AAG AGG
G GTT Valine GCT Alanine GAT Aspartic
acid
GGT Glycine
GTC GCC GAC GGC
GTA GCA GAA Glutamic
acid
GGA
GTG GCG GAG GGG

The genetic code (the "translation table" according to which DNA information is translated into amino acids, and hence proteins) is nearly identical for all known lifeforms, from bacteria and archaea to animals and plants. The universality of this code is generally regarded by biologists as definitive evidence in favor of universal common descent.[21]

The way that codons (DNA triplets) are mapped to amino acids seems to be strongly optimised. Richard Egel argues that in particular the hydrophobic (non-polar) side-chains are well organised, suggesting that these enabled the earliest organisms to create peptides with water-repelling regions able to support the essential electron exchange (redox) reactions for energy transfer.[23]

Selectively neutral similarities

Similarities which have no adaptive relevance cannot be explained by convergent evolution, and therefore they provide compelling support for universal common descent. Such evidence has come from two areas: amino acid sequences and DNA sequences. Proteins with the same three-dimensional structure need not have identical amino acid sequences; any irrelevant similarity between the sequences is evidence for common descent. In certain cases, there are several codons (DNA triplets) that code redundantly for the same amino acid. Since many species use the same codon at the same place to specify an amino acid that can be represented by more than one codon, that is evidence for their sharing a recent common ancestor. Had the amino acid sequences come from different ancestors, they would have been coded for by any of the redundant codons, and since the correct amino acids would already have been in place, natural selection would not have driven any change in the codons, however much time was available. Genetic drift could change the codons, but it would be extremely unlikely to make all the redundant codons in a whole sequence match exactly across multiple lineages. Similarly, shared nucleotide sequences, especially where these are apparently neutral such as the positioning of introns and pseudogenes, provide strong evidence of common ancestry.[24]

Other similarities

Biologists often point to the universality of many aspects of cellular life as supportive evidence to the more compelling evidence listed above. These similarities include the energy carrier adenosine triphosphate (ATP), and the fact that all amino acids found in proteins are left-handed. It is, however, possible that these similarities resulted because of the laws of physics and chemistry - rather than through universal common descent - and therefore resulted in convergent evolution. In contrast, there is evidence for homology of the central subunits of Transmembrane ATPases throughout all living organisms, especially how the rotating elements are bound to the membrane. This supports the assumption of a LUCA as a cellular organism, although primordial membranes may have been semipermeable and evolved later to the membranes of modern bacteria, and on a second path to those of modern archaea also.[25]

Phylogenetic trees

BacteriaArchaeaAquifexThermotogaCytophagaBacteroidesPlanctomycesCyanobacteriaProteobacteriaSpirochetesGram-positive bacteriaGreen filantous bacteriaPyrodicticumThermoproteusThermococcus celerMethanococcusMethanobacteriumMethanosarcinaHalophilesEntamoebaeSlime moldAnimalFungusPlantCiliateFlagellateTrichomonadMicrosporidiaDiplomonad
A phylogenetic tree based on ribosomal RNA genes implies a single origin for all life.

Another important piece of evidence is from detailed phylogenetic trees (i.e., "genealogic trees" of species) mapping out the proposed divisions and common ancestors of all living species. In 2010, Douglas L. Theobald published a statistical analysis of available genetic data,[1] mapping them to phylogenetic trees, that gave "strong quantitative support, by a formal test, for the unity of life."[2]

Traditionally, these trees have been built using morphological methods, such as appearance, embryology, etc. Recently, it has been possible to construct these trees using molecular data, based on similarities and differences between genetic and protein sequences. All these methods produce essentially similar results, even though most genetic variation has no influence over external morphology. That phylogenetic trees based on different types of information agree with each other is strong evidence of a real underlying common descent.[26]

Potential objections

2005 tree of life shows many horizontal gene transfers, implying multiple possible origins.

Gene exchange clouds phylogenetic analysis

Theobald noted that substantial horizontal gene transfer could have occurred during early evolution. Bacteria today remain capable of gene exchange between distantly-related lineages. This weakens the basic assumption of phylogenetic analysis, that similarity of genomes implies common ancestry, because sufficient gene exchange would allow lineages to share much of their genome whether or not they shared an ancestor (monophyly). This has led to questions about the single ancestry of life.[1] However, biologists consider it very unlikely that completely unrelated proto-organisms could have exchanged genes, as their different coding mechanisms would have resulted only in garble rather than functioning systems. Later, however, many organisms all derived from a single ancestor could readily have shared genes that all worked in the same way, and it appears that they have.[1]

Convergent evolution

If early organisms had been driven by the same environmental conditions to evolve similar biochemistry convergently, they might independently have acquired similar genetic sequences. Theobald's "formal test" was accordingly criticised by Takahiro Yonezawa and colleagues[27] for not including consideration of convergence. They argued that Theobald's test was insufficient to distinguish between the competing hypotheses. Theobald has defended his method against this claim, arguing that his tests distinguish between phylogenetic structure and mere sequence similarity. Therefore, Theobald argued, his results show that "real universally conserved proteins are homologous."[28][29]

See also

Bibliography

  • Crombie, A. C.; Hoskin, Michael (1970). "The Scientific Movement and the Diffusion of Scientific Ideas, 1688–1751". In Bromley, J. S. (ed.). The Rise of Great Britain and Russia, 1688–1715/25. The New Cambridge Modern History. 6. London: Cambridge University Press. ISBN 978-0-521-07524-4. LCCN 57014935. OCLC 7588392.CS1 maint: ref=harv (link)
  • Darwin, Charles (1859). On the Origin of Species by Means of Natural Selection, or the Preservation of Favoured Races in the Struggle for Life (1st ed.). London: John Murray. LCCN 06017473. OCLC 741260650.CS1 maint: ref=harv (link) The book is available from The Complete Work of Charles Darwin Online. Retrieved 2015-11-23.
  • Darwin, Erasmus (1818) [Originally published 1794]. Zoonomia; or the Laws of Organic Life. 1 (4th American ed.). Philadelphia, PA: Edward Earle.CS1 maint: ref=harv (link) Zoonomia; or The laws of organic life: in three parts (Volume 1) (1818) at the Internet Archive Retrieved 2015-11-23.
  • Harris, C. Leon (1981). Evolution: Genesis and Revelations: With Readings from Empedocles to Wilson. Albany, NY: State University of New York Press. ISBN 978-0-87395-487-7. LCCN 81002555. OCLC 7278190.CS1 maint: ref=harv (link)
  • Kant, Immanuel (1987) [Originally published 1790 in Prussia as Kritik der Urteilskraft]. Critique of Judgment. Translated, with an introduction, by Werner S. Pluhar; foreword by Mary J. Gregor. Indianapolis, IN: Hackett Publishing Company. ISBN 978-0-87220-025-8. LCCN 86014852. OCLC 13796153.CS1 maint: ref=harv (link)
  • Treasure, Geoffrey (1985). The Making of Modern Europe, 1648-1780. New York: Methuen. ISBN 978-0-416-72370-0. LCCN 85000255. OCLC 11623262.CS1 maint: ref=harv (link)

Notes

  1. Now called homology.

References

  1. Theobald, Douglas L. (13 May 2010). "A formal test of the theory of universal common ancestry". Nature. 465 (7295): 219–222. Bibcode:2010Natur.465..219T. doi:10.1038/nature09014. PMID 20463738.
  2. Steel, Mike; Penny, David (13 May 2010). "Origins of life: Common ancestry put to the test". Nature. 465 (7295): 168–169. Bibcode:2010Natur.465..168S. doi:10.1038/465168a. PMID 20463725.
  3. Doolittle, W. Ford (February 2000). "Uprooting the Tree of Life" (PDF). Scientific American. 282 (2): 90–95. Bibcode:2000SciAm.282b..90D. doi:10.1038/scientificamerican0200-90. PMID 10710791. Archived from the original (PDF) on 2006-09-07. Retrieved 2015-11-22.
  4. Glansdorff, Nicolas; Ying Xu; Labedan, Bernard (9 July 2008). "The Last Universal Common Ancestor: emergence, constitution and genetic legacy of an elusive forerunner". Biology Direct. 3: 29. doi:10.1186/1745-6150-3-29. PMC 2478661. PMID 18613974.
  5. Ohtomo, Yoko; Kakegawa, Takeshi; Ishida, Akizumi; et al. (January 2014). "Evidence for biogenic graphite in early Archaean Isua metasedimentary rocks". Nature Geoscience. 7 (1): 25–28. Bibcode:2014NatGe...7...25O. doi:10.1038/ngeo2025.
  6. Borenstein, Seth (13 November 2013). "Oldest fossil found: Meet your microbial mom". Yahoo News. Associated Press. Retrieved 2015-11-22.
  7. Noffke, Nora; Christian, Daniel; Wacey, David; Hazen, Robert M. (16 December 2013). "Microbially Induced Sedimentary Structures Recording an Ancient Ecosystem in the ca. 3.48 Billion-Year-Old Dresser Formation, Pilbara, Western Australia". Astrobiology. 13 (12): 1103–1124. Bibcode:2013AsBio..13.1103N. doi:10.1089/ast.2013.1030. PMC 3870916. PMID 24205812.
  8. Zimmer, Carl (4 May 2018). "The Very First Animal Appeared Amid an Explosion of DNA". The New York Times. Retrieved 4 May 2018.
  9. Paps, Jordi; Holland, Peter W. H. (30 April 2018). "Reconstruction of the ancestral metazoan genome reveals an increase in genomic novelty". Nature Communications. 9 (1730 (2018)): 1730. Bibcode:2018NatCo...9.1730P. doi:10.1038/s41467-018-04136-5. PMC 5928047. PMID 29712911.
  10. Darwin 1859, p. 490
  11. Crombie & Hoskin 1970, pp. 62–63
  12. Treasure 1985, p. 142
  13. Harris 1981, p. 107
  14. Kant 1987, p. 304: "Despite all the variety among these forms, they seem to have been produced according to a common archetype, and this analogy among them reinforces our suspicion that they are actually akin, produced by a common original mother."
  15. Darwin 1818, p. 397 [§ 39.4.8]
  16. Darwin 1859, p. 484
  17. Darwin, C. R. 1860. On the origin of species by means of natural selection, or the preservation of favoured races in the struggle for life. London: John Murray. 2nd edition, second issue, page 466
  18. Krogh, David. (2005). Biology: A Guide to the Natural World. Pearson/Prentice Hall. p. 323. ISBN 978-0321946768 "Descent with modification was accepted by most scientists not long after publication of Darwin's On the Origin of Species by Means of Natural Selection in 1859. Scientists accepted it because it explained so many facets of the living world."
  19. Kellogg, Vernon L. (1907). Darwinism To-Day. Henry Holt and Company. p. 3
  20. Gregory, T. Ryan (2008). "Evolution as Fact, Theory, and Path". Evolution: Education and Outreach. 1: 46–52. doi:10.1007/s12052-007-0001-z.
  21. Knight, Robin; Freeland, Stephen J.; Landweber, Laura F. (January 2001). "Rewiring the keyboard: evolvability of the genetic code". Nature Reviews Genetics. 2 (1): 49–58. doi:10.1038/35047500. PMID 11253070.
  22. Than, Ker (14 May 2010). "All Species Evolved From Single Cell, Study Finds". National Geographic. Retrieved 22 November 2017.
  23. Egel, Richard (March 2012). "Primal Eukaryogenesis: On the Communal Nature of Precellular States, Ancestral to Modern Life". Life. 2 (1): 170–212. doi:10.3390/life2010170. PMC 4187143. PMID 25382122.
  24. Sharma, N. S. (2005). Continuity And Evolution Of Animals. Mittal Publications. pp. 32–. ISBN 978-81-8293-018-6.
  25. Lane, Nick (2015). The Vital Question: Why Is Life The Way It Is?. Profile Books. ISBN 978-1781250365.
  26. Theobald, Douglas L. "Prediction 1.3: Consilience of independent phylogenies". 29+ Evidences for Macroevolution: The Scientific Case for Common Descent. Version 2.89. The TalkOrigins Foundation. Retrieved 2009-11-20.
  27. Yonezawa, Takahiro; Hasegawa, Masami (16 December 2010). "Was the universal common ancestry proved?". Nature. 468 (7326): E9. Bibcode:2010Natur.468E...9Y. doi:10.1038/nature09482. PMID 21164432.
  28. Theobald, Douglas L. (16 December 2010). "Theobald reply". Nature. 468 (7326): E10. Bibcode:2010Natur.468E..10T. doi:10.1038/nature09483.
  29. Theobald, Douglas L. (24 November 2011). "On universal common ancestry, sequence similarity, and phylogenetic structure: The sins of P-values and the virtues of Bayesian evidence". Biology Direct. 6 (1): 60. doi:10.1186/1745-6150-6-60. PMC 3314578. PMID 22114984.
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