Lineage (genetic)

The topic of Lineage (genetic) is an issue that has generated great interest and debate in recent times. With the advancement of technology and changes in society, Lineage (genetic) has become a crucial aspect that affects different areas of our lives. On a personal, professional, social and political level, the importance of Lineage (genetic) is undeniable. In this article we will explore different aspects related to Lineage (genetic), analyzing its impact and relevance in various contexts. From its origin to its evolution, through its implications and possible consequences, this topic does not leave anyone indifferent. In addition, we will try to shed light on the possible solutions or approaches that can be adopted against Lineage (genetic), with the aim of offering a global and complete vision of this issue that is so relevant today.

A genetic lineage includes all descendants of a given genetic sequence, typically following a new mutation. It is not the same as an allele because it excludes cases where different mutations give rise to the same allele, and includes descendants that differ from the ancestor by one or more mutations. The genetic sequence can be of different sizes, e.g. a single gene or a haplotype containing multiple adjacent genes along a chromosome. Given recombination, each gene can have a separate genetic lineages, even as the population shares a single organismal lineage. In asexual microbes or somatic cells, cell lineages exactly match genetic lineages, and can be traced.[1]

Incomplete lineage sorting

Main article: Incomplete lineage sorting
Figure 1. Incomplete lineage sorting. The gene G has two versions (alleles), G0 and G1. The ancestor of A, B and C originally had only one version of gene G, G0. At some point, a mutation occurred and the ancestral population became polymorphic, with some individuals having G0 and others G1. When species A split off, it retained only G1, while the ancestor of B and C remained polymorphic. When B and C diverged, B retained only G1 and C only G0; neither were now polymorphic in G. The tree for gene G shows A and B as sisters, whereas the species tree shows B and C as sisters.

Incomplete lineage sorting describes when the phylogenetic tree for a gene does not match that of the species. For example, while most human gene lineages coalesce first with chimpanzee lineages, and then with gorilla lineages, other configurations also occur.[2]

Lineage selection

Lineage selection occurs when the frequency of members of one lineage changes relative to another lineage. It is useful for studying alleles with complex effects that play out over multiple generations, e.g. alleles that affect recombination, evolvability, or altruism.[3][4] Lineage selection is also useful in determining the effects of mutations in highly structured environments such as tumors.[5]

Long-term stochastic outcomes of competition among lineages can be quantified within mathematical models as the ratio of fixation probability : counterfixation probability.[6] Inclusive fitness is equal to the average organismal fitness of individuals across the probability distribution of possible lineages.[7]

Tree sequence recording

Tree sequence recording describes efficient methods to record surviving lineages while conducting computer simulations of population genetics.[8] Resulting 'forward time' computer simulations offer an alternative to 'backward time' coalescent theory. Tree sequence recording has been incorporated into the population simulation software SLiM.[9]

Sexual lineages compared to asexual lineages

Sexual reproduction is the most common form of reproduction in the genetic lineages of multicellular organisms, and a complete lack of sexual reproduction is relatively rare among such organisms, particularly animals. Sexual reproduction appears to have emerged very early in the evolution of eukaryotes implying that the essential features of meiosis were already present in the earliest eukaryotic genetic lineage.[10][11]

Among eukaryotes, almost all lineages with asexual modes of reproduction maintain meiosis either in a modified form or as an alternative pathway.[12] A constraint on a meiotic sexual lineage undergoing switching to an ameiotic, asexual form of reproduction appears to be the concomitant loss of the protective recombinational repair of DNA damage that is a key function of meiosis.[13][14]

References

  1. ^ Levy, Sasha F.; Blundell, Jamie R.; Venkataram, Sandeep; Petrov, Dmitri A.; Fisher, Daniel S.; Sherlock, Gavin (March 2015). "Quantitative evolutionary dynamics using high-resolution lineage tracking". Nature. 519 (7542): 181–186. Bibcode:2015Natur.519..181L. doi:10.1038/nature14279. PMC 4426284. PMID 25731169.
  2. ^ Rivas-González, Iker; Rousselle, Marjolaine; Li, Fang; Zhou, Long; Dutheil, Julien Y.; Munch, Kasper; Shao, Yong; Wu, Dongdong; Schierup, Mikkel H.; Zhang, Guojie (2 June 2023). "Pervasive incomplete lineage sorting illuminates speciation and selection in primates". Science. 380 (6648). doi:10.1126/science.abn4409. PMID 37262154.
  3. ^ Graves, Christopher J.; Weinreich, Daniel M. (2 November 2017). "Variability in Fitness Effects Can Preclude Selection of the Fittest". Annual Review of Ecology, Evolution, and Systematics. 48 (1): 399–417. doi:10.1146/annurev-ecolsys-110316-022722. PMC 6768565. PMID 31572069.
  4. ^ De Vienne, Damien M.; Giraud, Tatiana; Gouyon, Pierre-Henri (2013). "Lineage Selection and the Maintenance of Sex". PLOS ONE. 8 (6e66906): e66906. Bibcode:2013PLoSO...866906D. doi:10.1371/journal.pone.0066906. PMC 3688966. PMID 23825582.
  5. ^ Nunney, Leonard (1999-03-07). "Lineage selection and the evolution of multistage carcinogenesis". Proceedings of the Royal Society of London B: Biological Sciences. 266 (1418): 493–498. doi:10.1098/rspb.1999.0664. ISSN 0962-8452. PMC 1689794. PMID 10189713.
  6. ^ King, Oliver D.; Masel, Joanna (December 2007). "The evolution of bet-hedging adaptations to rare scenarios". Theoretical Population Biology. 72 (4): 560–575. doi:10.1016/j.tpb.2007.08.006. PMC 2118055. PMID 17915273.
  7. ^ Akçay, Erol; Van Cleve, Jeremy (2016-02-05). "There is no fitness but fitness, and the lineage is its bearer". Phil. Trans. R. Soc. B. 371 (1687): 20150085. doi:10.1098/rstb.2015.0085. ISSN 0962-8436. PMC 4760187. PMID 26729925.
  8. ^ Kelleher, Jerome; Thornton, Kevin R.; Ashander, Jaime; Ralph, Peter L. (1 November 2018). "Efficient pedigree recording for fast population genetics simulation". PLOS Computational Biology. 14 (11): e1006581. Bibcode:2018PLSCB..14E6581K. doi:10.1371/journal.pcbi.1006581. PMC 6233923. PMID 30383757.
  9. ^ Haller, Benjamin C.; Galloway, Jared; Kelleher, Jerome; Messer, Philipp W.; Ralph, Peter L. (March 2019). "Tree-sequence recording in SLiM opens new horizons for forward-time simulation of whole genomes". Molecular Ecology Resources. 19 (2): 552–566. doi:10.1111/1755-0998.12968. PMC 6393187.
  10. ^ Dacks, Joel; Roger, Andrew J. (1999). "The First Sexual Lineage and the Relevance of Facultative Sex". Journal of Molecular Evolution. 48 (6): 779–783. Bibcode:1999JMolE..48..779D. doi:10.1007/PL00013156. ISSN 0022-2844. PMID 10229582. S2CID 9441768.
  11. ^ Bernstein, Harris; Bernstein, Carol (2010-08-01). "Evolutionary Origin of Recombination during Meiosis". BioScience. 60 (7): 498–505. doi:10.1525/bio.2010.60.7.5. ISSN 1525-3244. S2CID 86663600.
  12. ^ Hörandl, Elvira; Hadacek, Franz (2013). "The oxidative damage initiation hypothesis for meiosis". Plant Reproduction. 26 (4): 351–367. doi:10.1007/s00497-013-0234-7, PMC 3825497, PMID 23995700
  13. ^ Bernstein, H.; Hopf, F.A.; Michod, R.E. (1987). "The Molecular Basis of the Evolution of Sex". Molecular Genetics of Development. Advances in Genetics. Vol. 24. pp. 323–70. doi:10.1016/s0065-2660(08)60012-7, ISBN 9780120176243, PMID 3324702
  14. ^ Avise, J. (2008) Clonality: The Genetics, Ecology and Evolution of Sexual Abstinence in Vertebrate Animals. See pp. 22-25. Oxford University Press. ISBN 978-0-19-536967-0
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