History of genetics

Source: Wikipedia, the free encyclopedia.

The history of genetics dates from the

His works on pea plants, published in 1866, provided the initial evidence that, on its rediscovery in 1900's, helped to establish the theory of Mendelian inheritance
.

In

's book On Animal Generation contradicted Aristotle's theories of genetics and embryology.

The 1900 rediscovery of Mendel's work by

Mendelian model, which was widely accepted by 1925. Alongside experimental work, mathematicians developed the statistical framework of population genetics, bringing genetic explanations into the study of evolution
.

With the basic patterns of genetic inheritance established, many biologists turned to investigations of the physical nature of the gene. In the 1940s and early 1950s, experiments pointed to DNA as the portion of chromosomes (and perhaps other nucleoproteins) that held genes. A focus on new model organisms such as viruses and bacteria, along with the discovery of the double helical structure of DNA in 1953, marked the transition to the era of molecular genetics.

In the following years, chemists developed techniques for sequencing both nucleic acids and proteins, while many others worked out the relationship between these two forms of biological molecules and discovered the genetic code. The regulation of gene expression became a central issue in the 1960s; by the 1970s gene expression could be controlled and manipulated through genetic engineering. In the last decades of the 20th century, many biologists focused on large-scale genetics projects, such as sequencing entire genomes.

Pre-Mendel ideas on heredity

Ancient theories

Aristotle's model of transmission of movements from parents to child, and of form from the father. The model is not fully symmetric.[1]

The most influential early theories of heredity were that of

inheritance of acquired characters was a supposedly well-established fact that any adequate theory of heredity had to explain. At the same time, individual species were taken to have a fixed essence; such inherited changes were merely superficial.[2] The Athenian philosopher Epicurus observed families and proposed the contribution of both males and females of hereditary characters ("sperm atoms"), noticed dominant and recessive types of inheritance and described segregation and independent assortment of "sperm atoms".[3]

In the 9th century CE, the

Preformation theory

Sperms as preformed humans. Painting of Nicolaas Hartsoeker 1695

The preformation theory is a developmental biological theory, which was represented in antiquity by the Greek philosopher Anaxagoras. It reappeared in modern times in the 17th century and then prevailed until the 19th century. Another common term at that time was the theory of evolution, although "evolution" (in the sense of development as a pure growth process) had a completely different meaning than today. The preformists assumed that the entire organism was preformed in the sperm (animalkulism) or in the egg (ovism or ovulism) and only had to unfold and grow. This was contrasted by the theory of epigenesis, according to which the structures and organs of an organism only develop in the course of individual development (Ontogeny). Epigenesis had been the dominant opinion since antiquity and into the 17th century, but was then replaced by preformist ideas. Since the 19th century epigenesis was again able to establish itself as a view valid to this day.[7][8]

Plant systematics and hybridisation

In the 18th century, with increased knowledge of plant and animal diversity and the accompanying increased focus on

back-crosses.[9]

Plant breeders were also developing an array of stable

Gartons Agricultural Plant Breeders in England explained their system.[11]

Mendel

Blending Inheritance

Between 1856 and 1865, Gregor Mendel conducted breeding experiments using the pea plant Pisum sativum and traced the inheritance patterns of certain traits. Through these experiments, Mendel saw that the genotypes and phenotypes of the progeny were predictable and that some traits were dominant over others.[12] These patterns of Mendelian inheritance demonstrated the usefulness of applying statistics to inheritance. They also contradicted 19th-century theories of blending inheritance, showing, rather, that genes remain discrete through multiple generations of hybridisation.[13]

From his statistical analysis, Mendel defined a concept that he described as a character (which in his mind holds also for "determinant of that character"). In only one sentence of his historical paper, he used the term "factors" to designate the "material creating" the character: " So far as experience goes, we find it in every case confirmed that constant progeny can only be formed when the egg cells and the fertilising pollen are off like the character so that both are provided with the material for creating quite similar individuals, as is the case with the normal fertilisation of pure species. We must, therefore, regard it as certain that exactly similar factors must be at work also in the production of the constant forms in the hybrid plants."(Mendel, 1866).

Mendelian inheritance states characteristics are discrete and are inherited by the parents. This image depicts a monohybrid cross and shows 3 generations: P1 generation (1), F1 generation (2), and F2 generation (3). Each organism inherits two alleles, one from each parent, that make up the genotype. The observed characteristic, the phenotype, is determined by the dominant allele in the genotype. In this monohybrid cross the dominant allele encodes for the colour red and the recessive allele encodes for the colour white.

Mendel's work was published in 1866 as "Versuche über Pflanzen-Hybriden" (

Experiments on Plant Hybridisation) in the Verhandlungen des Naturforschenden Vereins zu Brünn (Proceedings of the Natural History Society of Brünn), following two lectures he gave on the work in early 1865.[14]

Post-Mendel, pre-rediscovery

Pangenesis

gemmules, which migrate to the gonads and contribute to the fertilised egg and so to the next generation. The theory implied that changes to the body during an organism's life would be inherited, as proposed in Lamarckism
.

Mendel's work was published in a relatively obscure

Lamarckian heredity seemed to be required. Darwin's own theory of heredity, pangenesis, did not meet with any large degree of acceptance.[15][16] A more mathematical version of pangenesis, one which dropped much of Darwin's Lamarckian holdovers, was developed as the "biometrical" school of heredity by Darwin's cousin, Francis Galton.[17]

Germ plasm

August Weismann's germ plasm theory. The hereditary material, the germ plasm, is confined to the gonads. Somatic cells (of the body) develop afresh in each generation from the germ plasm.

In 1883 August Weismann conducted experiments involving breeding mice whose tails had been surgically removed. His results — that surgically removing a mouse's tail had no effect on the tail of its offspring — challenged the theories of pangenesis and Lamarckism, which held that changes to an organism during its lifetime could be inherited by its descendants. Weismann proposed the germ plasm theory of inheritance, which held that hereditary information was carried only in sperm and egg cells.[18]

Rediscovery of Mendel

Hugo de Vries wondered what the nature of germ plasm might be, and in particular he wondered whether or not germ plasm was mixed like paint or whether the information was carried in discrete packets that remained unbroken. In the 1890s he was conducting breeding experiments with a variety of plant species and in 1897 he published a paper on his results that stated that each inherited trait was governed by two discrete particles of information, one from each parent, and that these particles were passed along intact to the next generation. In 1900 he was preparing another paper on his further results when he was shown a copy of Mendel's 1866 paper by a friend who thought it might be relevant to de Vries's work. He went ahead and published his 1900 paper without mentioning Mendel's priority. Later that same year another botanist, Carl Correns, who had been conducting hybridisation experiments with maize and peas, was searching the literature for related experiments prior to publishing his own results when he came across Mendel's paper, which had results similar to his own. Correns accused de Vries of appropriating terminology from Mendel's paper without crediting him or recognising his priority. At the same time another botanist, Erich von Tschermak was experimenting with pea breeding and producing results like Mendel's. He too discovered Mendel's paper while searching the literature for relevant work. In a subsequent paper de Vries praised Mendel and acknowledged that he had only extended his earlier work.[18]

Emergence of molecular genetics

After the rediscovery of Mendel's work there was a feud between

The Correlation Between Relatives on the Supposition of Mendelian Inheritance
".

sex linked inheritance of the white eyed mutation in the fruit fly Drosophila in 1910, implying the gene was on the sex chromosome
.

In 1910,

fly room, using Drosophila melanogaster, provided the first chromosomal map of any biological organism. In 1928, Frederick Griffith showed that genes could be transferred. In what is now known as Griffith's experiment, injections into a mouse of a deadly strain of bacteria
that had been heat-killed transferred genetic information to a safe strain of the same bacteria, killing the mouse.

A series of subsequent discoveries (e.g.

James D. Watson and Francis Crick demonstrated the molecular structure of DNA in 1953.[23]
.

In 1947 Salvador Luria discovered the reactivation of irradiated phage[25] leading to many further studies on the fundamental processes of repair of DNA damage (for review of early studies, see [26]). In 1958 Meselson and Stahl demonstrated that DNA replicates semiconservatively, leading to the understanding that each of the individual strands in double-stranded DNA serves as a template for new strand synthesis.[27] In 1960 Jacob and collaborators discovered the operon which consists of a sequence of genes whose expression is coordinated by operator DNA.[28] In the period 1961 – 1967, through work in several different labs, the nature of the genetic code was determined (e.g. [29]).

In 1972,

continuum".[31][32] It was first hypothesised in 1986 by Walter Gilbert
that neither DNA nor protein would be required in such a primitive system as that of a very early stage of the earth if RNA could serve both as a catalyst and as genetic information storage processor.

The modern study of genetics at the level of DNA is known as molecular genetics and the synthesis of molecular genetics with traditional Darwinian evolution is known as the modern evolutionary synthesis.

See also

References

  1. ^ a b Leroi, Armand Marie (2010). Föllinger, S. (ed.). Function and Constraint in Aristotle and Evolutionary Theory. Franz Steiner Verlag. pp. 215–221. {{cite book}}: |work= ignored (help)
  2. ^ Mayr, The Growth of Biological Thought, pp 635–640
  3. ^ Yapijakis C. (2017) Ancestral Concepts of Human Genetics and Molecular Medicine in Epicurean Philosophy. In: Petermann H., Harper P., Doetz S. (eds) History of Human Genetics. Springer, Cham
  4. JSTOR 984852
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  6. Ibn Tibon
    , p.375: ונראה כזה בענין הטבעי, כי כמה יש מבני האדם שאינו דומה לאב כלל אך הוא דומה לאבי אביו ואין ספק כי הטבע ההוא והדמיון ההוא היה צפון באב ואף על פי שלא נראה להרגשה
  7. ^ Ilse Jahn, Rolf Löther, Konrad Senglaub (Editor): Geschichte der Biologie. Theorien, Methoden, Institutionen, Kurzbiographien. 2nd edition. VEB Fischer, Jena 1985
  8. ^ Mayr, The Growth of Biological Thought, pp 640–649
  9. ^ Mayr, The Growth of Biological Thought, pp 649–651
  10. ^ For example, Explanatory Notes, Gartons Seed Catalogue for Spring 1901
  11. .
  12. ^ Mukherjee, Siddartha (2016) The Gene: An intimate history Chapter 4.
  13. ISSN 1059-1028
    . Retrieved 11 November 2019.
  14. ^ Darwin, C. R. (1871). Pangenesis. Nature. A Weekly Illustrated Journal of Science 3 (27 April): 502–503.
  15. PMID 4908353
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  17. ^ a b Mukherjee, Siddartha (2016) The Gene:An intimate history Chapter 5.
  18. ^ HERSHEY AD, CHASE M. Independent functions of viral protein and nucleic acid in growth of bacteriophage. J Gen Physiol. 1952 May;36(1):39-56. doi: 10.1085/jgp.36.1.39. PMID: 12981234; PMCID: PMC2147348
  19. ^ Beadle GW, Tatum EL. Genetic Control of Biochemical Reactions in Neurospora. Proc Natl Acad Sci U S A. 1941 Nov 15;27(11):499-506. doi: 10.1073/pnas.27.11.499. PMID: 16588492; PMCID: PMC1078370
  20. PMID 17567988
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  23. ^ WATSON JD, CRICK FH. Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid. Nature. 1953 Apr 25;171(4356):737-8. doi: 10.1038/171737a0. PMID: 13054692
  24. ^ Luria SE. Reactivation of Irradiated Bacteriophage by Transfer of Self-Reproducing Units. Proc Natl Acad Sci U S A. 1947 Sep;33(9):253-64. doi: 10.1073/pnas.33.9.253. PMID: 16588748; PMCID: PMC1079044
  25. ^ Bernstein C. Deoxyribonucleic acid repair in bacteriophage. Microbiol Rev. 1981 Mar;45(1):72-98. doi: 10.1128/mr.45.1.72-98.1981. PMID: 6261109; PMCID: PMC281499
  26. ^ Meselson M, Stahl FW. THE REPLICATION OF DNA IN ESCHERICHIA COLI. Proc Natl Acad Sci U S A. 1958 Jul 15;44(7):671-82. doi: 10.1073/pnas.44.7.671. PMID: 16590258; PMCID: PMC528642
  27. ^ Jacob F, Perrin D, Sánchez C, Monod J, Edelstein S. The operon: a group of genes with expression coordinated by an operator. C.R.Acad. Sci. Paris 250 (1960) 1727-1729. C R Biol. 2005 Jun;328(6):514-20. English, French. doi: 10.1016/j.crvi.2005.04.005. PMID: 15999435
  28. ^ CRICK FH, BARNETT L, BRENNER S, WATTS-TOBIN RJ. General nature of the genetic code for proteins. Nature. 1961 Dec 30;192:1227-32. doi: 10.1038/1921227a0. PMID: 13882203
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  31. .

Further reading

External links