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Weismann barrier

From Wikipedia, the free encyclopedia
Distinction between germ cell lineages producing gametes and somatic cells
Diagram ofAugust Weismann'sgerm plasm theory. The hereditary material, the germ plasm, is confined to thegonads. Somatic cells (of the body)develop afresh in each generation from the germ plasm. Whatever may happen to those cells does not affect the next generation.

TheWeismann barrier, proposed byAugust Weismann, is the strict distinction between the "immortal" germ cell lineages producing gametes and "disposable" somatic cells in animals (but not plants), in contrast toCharles Darwin's proposedpangenesis mechanism for inheritance.[1][2]

In more precise terminology, hereditary information is copied only fromgermline cells tosomatic cells. This means that new information from somatic mutation is not passed on to the germline. Thisbarrier concept implies that somatic mutations are not inherited.[3][4]

Weismann set out the concept in his 1892 book ″Das Keimplasma: eine Theorie der Vererbung″ (German forTheGerm Plasm: a theory of inheritance).[5] The use of this theory, commonly in the context of thegerm plasm theory of the late 19th century, before the development of better-based and more sophisticated concepts of genetics in the early 20th century, is sometimes referred to asWeismannism.[6] Some authors distinguishWeismannist development (eitherpreformistic orepigenetic) that in which there is a distinct germline, fromsomatic embryogenesis.[7] This type of development is correlated with theevolution of death of the somatic line.

The Weismann barrier was of great importance in its day and among other influences it effectively banished certainLamarckian concepts: in particular, it would make Lamarckian inheritance from changes to the body (the soma) difficult or impossible.[8] It remains important, but has however required qualification in the light of modern understanding ofhorizontal gene transfer and some other genetic and histological developments.[9]

Immortality of the germline

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The Russian biologist and historianZhores A. Medvedev, reviewing Weismann's theory a century later, considered that the accuracy ofgenome replicative and other synthetic systems alone could not explain the "immortal"germ cell lineages proposed by Weismann. Rather Medvedev thought that known features of the biochemistry and genetics ofsexual reproduction indicated the presence of unique information maintenance and restoration processes at the different stages ofgametogenesis. In particular, Medvedev considered that the most important opportunities for information maintenance ofgerm cells are created byrecombination during meiosis andDNA repair; he saw these as processes within the germ cells that were capable of restoring the integrity ofDNA andchromosomes from the types of damage that caused irreversible ageing insomatic cells.[10]

Basal animals

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Basal animals such as sponges (Porifera) and corals (Anthozoa) contain multipotent stem cell lineages, that give rise to both somatic and reproductive cells. The Weismann barrier appears to be of a more recent evolutionary origin among animals.[11]

Plants

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In plants, genetic changes in somatic lines can and do result in genetic changes in the germ lines, because the germ cells are produced by somatic cell lineages (vegetativemeristems), which may be old enough (many years) to have accumulated multiple mutations since seed germination, some of them subject to natural selection.[12] It is noteworthy in this context that, generally speaking, adult, reproducing plants tend to produce many more offspring in number than animal organisms.

See also

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References

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  1. ^Geison, G. L. (1969). "Darwin and heredity: The evolution of his hypothesis of pangenesis".J Hist Med Allied Sci.XXIV (4):375–411.doi:10.1093/jhmas/XXIV.4.375.PMID 4908353.
  2. ^You, Yawen (26 January 2015)."The Germ-Plasm: a Theory of Heredity (1893), by August Weismann".The Embryo Project Encyclopedia (Arizona State University). Retrieved7 September 2018.
  3. ^Gauthier, Peter (March–May 1990). "Does Weismann's Experiment Constitute a Refutation of the Lamarckian Hypothesis?".BIOS.61 (1/2):6–8.JSTOR 4608123.
  4. ^This does not refer to thecentral dogma of molecular biology, which states that no sequential information can travel fromprotein toDNA orRNA, but both hypotheses relate to a gene-centric view of life.De Tiege, Alexis; Tanghe, Koen; Braeckman, Johan; Van de Peer, Yves (January 2014). "From DNA- to NA-centrism and the conditions for gene-centrism revisited".Biology & Philosophy.29 (1):55–69.doi:10.1007/s10539-013-9393-z.S2CID 85866639.
  5. ^Weismann, August (1892).Das Keimplasma: eine Theorie der Vererbung. Jena: Fischer.
  6. ^Romanes, George John (1893).An examination of Weismannism. Chicago: Open court.OL 23380098M.
  7. ^Ridley, Mark (2004).Evolution (3rd ed.). Blackwell. pp. 295–297.
  8. ^Romanes, George John (1893).An examination of Weismannism. Open Court.OL 23380098M.
  9. ^Lindley, Robyn A."How Mutational and Epigenetic Changes Enable Adaptive Evolution".G. I. T. Laboratory Journal. Archived fromthe original on 2011-08-29. Retrieved2018-09-07.
  10. ^Medvedev, Zhores A. (1981). "On the immortality of the germ line: Genetic and biochemical mechanisms. A review".Mechanisms of Ageing and Development.17 (4):331–359.doi:10.1016/0047-6374(81)90052-X.ISSN 0047-6374.PMID 6173551.S2CID 35719466.
  11. ^Radzvilavicius, Arunas L.; Hadjivasiliou, Zena; Pomiankowski, Andrew; Lane, Nick (2016-12-20)."Selection for Mitochondrial Quality Drives Evolution of the Germline".PLOS Biology.14 (12) e2000410.doi:10.1371/journal.pbio.2000410.ISSN 1545-7885.PMC 5172535.PMID 27997535.
  12. ^Whitham, T.G.; Slobodchikoff, C.N. (1981). "Evolution by individuals, plant-herbivore interactions, and mosaics of genetic variability: The adaptive significance of somatic mutations in plants".Oecologia.49 (3):287–292.Bibcode:1981Oecol..49..287W.doi:10.1007/BF00347587.PMID 28309985.S2CID 20411802.
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