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Thomas Hunt Morgan

 

(born Sept. 25, 1866, Lexington, Ky., U.S. — died Dec. 4, 1945, Pasadena, Calif.) U.S. zoologist and geneticist. He received his doctorate from Johns Hopkins University. As a professor at Columbia University (1904 – 28) and California Institute of Technology (1928 – 45), he conducted important research on heredity. Like many of his contemporaries, Morgan found Charles Darwin's theory of natural selection implausible because it could not be tested experimentally, and he objected to Mendelian and chromosome theories, arguing that no single chromosome could carry specific hereditary traits. His opinion changed as a result of his studies of Drosophila. He developed the hypothesis of sex-linked traits. He adopted the term gene and concluded that genes were possibly arranged in a linear fashion on chromosomes. He was awarded the Nobel Prize in 1933. See also Calvin Blackman Bridges.

For more information on Thomas Hunt Morgan, visit Britannica.com.

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Scientist: Thomas Hunt Morgan
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Thomas Hunt Morgan
Library of Congress

[b. Lexington, Kentucky, September 25, 1866, d. Pasadena, California, December 4, 1945]

Working mainly with the small fruit fly Drosophila melanogaster, Morgan concluded that genes are arranged in a line on chromosomes and that chromosomes are present in the nucleus of every living cell. Morgan also noted occasional recombinations of inherited characteristics and proposed that this results from an exchange of genes between the two chromosomes of a pair, a process he named crossing over.


Genetics Encyclopedia: Thomas Hunt Morgan
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Geneticist 1866-1945

Thomas Hunt Morgan proved the validity of the chromosomal theory of heredity and led a research group whose insights into the physical nature of inheritance propelled genetics into the center of biology in the twentieth century.

Training and Early Interests

Morgan was born and raised in Kentucky, and received his bachelor's degree from the State College of Kentucky in 1886. He pursued graduate study at Johns Hopkins University in Baltimore, and eventually became a professor of biology at Bryn Mawr College in 1891. His early interests were in developmental biology and evolution. After moving to Columbia University in 1901 and coming under the influence of the great cell biologist Edwin Wilson, Morgan turned his attention to understanding the physical basis of inheritance, which he saw as a means to test theories about the role of mutation in evolution.

At the time Morgan began his work, chromosomes had been seen in cells, but their significance was unknown and not widely considered. A student of Wilson's, Walter Sutton, had recently proposed that chromosomes carried the genetic material, but had little evidence to support this important hypothesis. At the time, the gene itself was an abstract concept with no known physical correlate, and many scientists thought it was not a physical entity at all, but only a convenient fiction for describing some experimental results. In fact, it was Morgan's use of the term "gene" that helped bring it into general use in science.

To attack the issue of heredity, Morgan chose to work with the fruit fly, Drosophila melanogaster. This fly requires little space, breeds quickly, has many observable characteristics, and has only four chromosomes, making it an ideal model organism for genetics studies. Morgan also gathered a trio of very bright students, Hermann Muller, Alfred Sturtevant, and Calvin Bridges, and cultivated an egalitarian system of collaboration that was unknown in most other labs. The combination of the right question, the right model, the right collaborators, and some luck allowed Morgan and his group in their lab, dubbed "The Fly Room," to make their fundamental discoveries. Beginning in 1908, they proved that chromosomes do indeed carry the genes, that genes are discrete physical things arranged on chromosomes like beads on a string, that genes change places on chromosomes, that genes can be mutated and those mutations are faithfully inherited, and that mutations can be caused by exposure to high-energy radiation or other environmental phenomena.

A Lucky Discovery

This long string of seminal discoveries began with the discovery of a single male white-eyed fly among the many thousands of normal red-eyed ones. Morgan bred this mutant male with a red-eyed female. All the offspring were red-eyed, indicating the white form of the gene (called the white allele) was "recessive" to the dominant red allele: Flies carried the mutant allele, but its effects did not show up. When these offspring were crossed, the ratio of red to white was 3:1, just what would be expected for a classical recessive trait.

However, Morgan noted an unusual fact about the white-eyed flies—all of them were male. Morgan knew that the female Drosophila had two so-called X chromosomes, while the male had only one. Combining this fact with his discovery that only males showed the white-eye trait, he reasoned that the white-eye mutant allele must be on the X chromosome. Males show the white-eye trait because the mutant white allele is the only one they have—they don't have a second X chromosome with a normal red allele. Females rarely show the white-eye trait, because they have a normal redeye allele on the other X chromosome.

Morgan's results showed that the white-eye allele is inherited on the X chromosome, and confirmed the discovery that the X chromosome helps determine sex, first shown in 1905 by Sutton and Nettie Stevens. In one step, his discovery proved that genes, the factors governing inheritance, are carried on chromosomes, and that specific genes are carried on specific chromosomes. This provided the crucial evidence that genes are indeed discrete physical objects.

Linkage and Chromosome Mapping

The discovery of more mutated genes allowed Morgan's group to explore how genes are arranged on the chromosome, and to discover an exception to one of Mendel's laws of inheritance. Mendel had proposed the Law of Independent Assortment, stating that the alternative forms of different traits (such as round versus wrinkled pea seeds and short versus tall plant height) separate and recombine independently of each other, so that, for instance, obtaining a wrinkled tall plant is just as likely as obtaining a wrinkled short plant.

Morgan found this was not always true. Rather, certain combinations of alleles are very unlikely to be separated from each other, a fact he attributed to co-inheritance of the two alleles on the same chromosome. While alleles on separate chromosomes assort independently, as Mendel predicted, those on the same chromosome travel together unless separated.

To explore this, Morgan crossed a red-eyed fly with normal-length wings with a purple-eyed fly with stubby wings. After two generations, Mendel's laws predicted that all possible combinations of eye color and wing length should be equally likely. Instead, Morgan found that most flies had the original trait combinations, while red-eyed, stubby-winged flies were rare, as were purple-eyed, normal-winged flies. He concluded that the genes for wing length and purple eye color were on the same chromosome. Like passengers traveling on the same ship, once the particular alleles were together, they tended to stay linked. (Note that the purple eye-color gene is not the same one as the red-white eye-color gene he discovered previously, and is not on the X chromosome.)

However, Morgan noted specific allele combinations didn't always stay together: There were a few flies whose stubby-wing allele and purple-eye allele had become separated from each other. This led Morgan to propose that chromosomes sometimes exchange segments, allowing their passengers to change vessels, so to speak. This phenomenon is known as crossing over, and was later conclusively demonstrated in maize by Barbara McClintock.

Crossing over is now known to occur only during meiosis, the chromosome division that leads to formation of eggs and sperm. During meioisis, homologous chromosomes originally donated from the mother and father pair up for an extended period. In this period, called synapsis, the maternal and paternal chromosomes randomly exchange several segments, resulting in a pair of chromosomes with a mix of maternally derived and paternally derived alleles. These then separate to form the eggs and sperm.

Morgan's student Sturtevant reasoned that the likelihood of two alleles becoming separated during crossing over was proportional to the distance between them. In other words, the closer they are, the more likely they will stay together, and the further apart they are, the more likely they will separate. If A, B, and C are on the same chromosome, and A stays with B more often than it stays with C, then the distance from A to B is shorter than the distance from A to C. In this way, the relative distances of genes can be determined, providing a "linkage map" of the chromosomes. The unit of relative distance is called the morgan, in honor of Morgan himself. Calvin Bridges later devised a method to determine the absolute distance between genes, relying on the distinct banding patterns seen in Drosophila chromosomes in the larval stage.

Morgan's Legacy

In 1915 Morgan, Bridges, Sturtevant, and Muller published The Mechanism of Mendelian Heredity, a highly influential textbook laying out the evidence for the chromosomal theory of heredity and illustrating their methods so others could apply them in further research. In 1928 Morgan moved to the California Institute of Technology to found the Division of Biology. Sturtevant and Bridges went with him. Five years later Morgan was awarded the Nobel Prize in physiology or medicine for his work in genetics. He shared the prize money with Sturtevant and Bridges. Besides his own discoveries, Morgan's intellectual legacy includes the historically important researchers who trained with him, including Theodosius Dobzhansky, who applied the new genetics to an understanding of evolution. Another of his students was George Beadle, who discovered that mutations affect the working of proteins, and proposed the "one gene-one enzyme" definition of the gene.

Bibliography

Allen, Garland E. Thomas Hunt Morgan: The Man and His Science. Princeton, NJ:Princeton University Press, 1978.

Judson, Horace F. The Eighth Day of Creation: The Makers of the Revolution in Biology.New York: Simon & Schuster, 1979.

Morgan, Thomas Hunt, et al. The Mechanism of Mendelian Heredity. New York: HoltRinehart & Winston, 1915. Reprint, with an introduction by Garland E. Allen, New York: Johnson Reprint Corporation, 1978.

Sturtevant, Alfred H. A History of Genetics. New York: Harper & Row, 1965.

—Richard Robinson

Biography: Thomas Hunt Morgan
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The American zoologist and geneticist Thomas Hunt Morgan (1866-1945) established the theory of the gene which helped clarify the process of evolution and formed the modern basis of heredity.

Thomas Hunt Morgan, born on Sept. 25, 1866, in Lexington, Ky., was the son of Charlton and Ellen Morgan. He was descended on both sides from English Cavalier stock. In 1886 he entered the State College of Kentucky and later studied at Johns Hopkins University, where he divided his time between morphology and physiology. In 1890 he received his doctorate for a paper on the embryology and phylogeny of sea spiders. In 1891 he served as professor of biology at Bryn Mawr College, after which he went to Europe for further study, first in Germany and then at the famous zoological station at Naples, Italy. There he met Hans Driesch, the philosopher-scientist who believed in "vitalism." Morgan, however, favored a mechanistic approach to the solution of biological problems.

Upon his return to the United States in 1904, Morgan accepted a professorship at Columbia University which lasted until 1928. While there he undertook a series of breeding experiments to assess the reality of genes as the particles of heredity. Morgan chose the fruit fly (Drosophila melanogaster) for his experiments because it was a short-lived organism that could easily be bred in the laboratory under changing condition and could complete its life cycle in about 10 days, supplying as many as 30 generations a year.

Morgan's experiments were so successful that by 1914 he had proved the chromosome theory of heredity as a result of breeding and cytological examination. In 1910 he found his first mutant and proceeded to cross this fly with a normal one. The percentages of normal and mutant off-spring were in accordance with Mendel's law of inheritance. Morgan found many mutant characters and soon discovered that certain characteristics not only were sex-linked but also tended to appear together in certain flies. From this he postulated that all sex-linked characters tended to be inherited together because they were associated as a unit on a single chromosome in the nucleus of the original cell. Morgan called these characters linkage groups. By the summer of 1914 three linkage groups had been discovered. He used the word "gene" to represent each character unit, and the exact positions of these genes in the chromosomes was worked out by Alfred Henry Sturtevant, one of Morgan's former students and a member of his research staff. In 1915 Morgan and his assistants published The Mechanism of Mendelian Heredity to describe the system of genes. Later he published The Theory of the Gene (1926), his culminating work on the subject which discussed at length the chromosome theory of heredity.

In 1928 Morgan established the Kerckhoff Laboratories of Biological Sciences at the California Institute of Technology in Pasadena, which became the leading center for research genetics. In 1933 he received the Nobel Prize in physiology or medicine in recognition of the significance of his theory of heredity for physiology and for the part that the new genetics was destined to play in the future of medicine.

In 1941 Morgan retired as active head of his department at Cal Tech. However, he continued to work on problems in embryology which he had first approached in 1903 - trying to find out why the spermatozoon of the common hermaphroditic sea squirt almost never fertilizes the egg of the same individual (self-sterilization) but does fertilize eggs of all other sea squirts. On Dec. 4, 1945, the grand old man of genetics passed away.

Further Reading

No full-length biography or autobiography of Morgan has been published. A detailed account of his life and work is in Bernard Jaffe, Men of Science in America (1944; rev. ed. 1958). A biography also appears in National Academy of Sciences, Biographical Memoirs, vol. 33 (1959). Short studies of Morgan are in Theodore L. Sourkes, Nobel Prize Winners in Medicine and Physiology, 1901-1965 (1953; rev. ed. 1967); Katherine Binney Shippen, Men, Microscopes and Living Things (1955); Jay E. Greene, ed., 100 Great Scientists (1964); and Nobel Foundation, Physiology or Medicine: Nobel Lectures, including Presentation Speeches and Laureates' Biographies (3 vols., 1964-1967).

 
Columbia Encyclopedia: Thomas Hunt Morgan
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Morgan, Thomas Hunt, 1866-1945, American zoologist, b. Lexington, Ky., Ph.D. Johns Hopkins, 1890. He was professor of experimental zoology at Columbia (1904-28) and from 1928 was director of the laboratory of biological sciences at the California Institute of Technology. He is noted for his ingenious demonstration of the physical basis of heredity and the importance of the gene, using in his research the fruit fly, Drosophila. He described the phenomena of linkage and crossing over, which he and his students utilized to map the linear arrangement of genes along the chromosome. Morgan received the 1933 Nobel Prize in Physiology or Medicine. His books, classics in the literature of genetics, include The Physical Basis of Heredity (1919), Mechanism of Mendelian Heredity (rev. ed. 1923), Evolution and Genetics (1925), The Theory of the Gene (rev. ed. 1928), and Embryology and Genetics (1934).
Wikipedia: Thomas Hunt Morgan
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Thomas Hunt Morgan

Johns Hopkins yearbook of 1891
Born September 25, 1866(1866-09-25)
Lexington, Kentucky
Died December 4, 1945 (aged 79)
Pasadena, California
Nationality United States
Fields geneticist
embryologist
Institutions Bryn Mawr College
Columbia University
California Institute of Technology
Alma mater University of Kentucky
Johns Hopkins University
Doctoral students John Howard Northrop
Known for Drosophila melanogaster
Notable awards Nobel Prize in Physiology
or Medicine
in 1933

Thomas Hunt Morgan (September 25, 1866 – December 4, 1945) was an American geneticist and embryologist. Morgan received his PhD from Johns Hopkins University in 1890 and researched embryology during his tenure at Bryn Mawr. Following the rediscovery of Mendelian inheritance in 1900, Morgan's research moved to the study of mutation in the fruit fly Drosophila melanogaster. In his famous Fly Room at Columbia University Morgan was able to demonstrate that genes are carried on chromosomes and are the mechanical basis of heredity. These discoveries formed the basis of the modern science of genetics. When he was awarded the Nobel Prize in Physiology or Medicine in 1933 he was the first person awarded the Prize in genetics, for his discoveries concerning the role played by the chromosome in heredity.[1]

During his distinguished career, Morgan wrote 22 books[2] and 370 scientific papers,[3] and, as a result of his work, Drosophila became a major model organism in contemporary genetics. The Division of Biology he established at the California Institute of Technology produced seven Nobel Prize winners.

Contents

Early life

Morgan was born in Lexington, Kentucky, to Charlton Hunt Morgan and Ellen Key Howard Morgan.[4] Part of a long line of Southern aristocracy on his father's side, Morgan was a nephew of Confederate General John Hunt Morgan and his great-grandfather John Wesley Hunt had been the first millionaire west of the Allegheny Mountains. Through his mother, he was the great-grandson of Francis Scott Key, the author of the "Star Spangled Banner", and John Eager Howard, a one-time governor and senator from Maryland.[4] However, following the Civil War the family had fallen on harder times with the loss of civil and property rights for those who aided the Confederacy. His father also had difficulty finding work in politics and spent much of his time coordinating veterans reunions.

Beginning at age 16 in the Preparatory Department, Morgan attended the State College of Kentucky (now the University of Kentucky). There, he focused on science; he particularly enjoyed natural history, and worked with the U.S. Geological Survey in his summers. He graduated as valedictorian in 1886 and was the only student[citation needed] to graduate with a bachelor in science.[5] Following a summer at the Marine Biology School in Annisquam, Massachusetts, Morgan began graduate studies in zoology at the recently founded Johns Hopkins University, the first research-oriented American university. After two years of experimental work with morphologist William Keith Brooks and several publications, Morgan was eligible to receive a master of science from the State College of Kentucky in 1888, the College required two years study at another institution and an examination by the College Faculty.[citation needed] The College offered Morgan a full professorship; however, he chose to stay at Johns Hopkins and was awarded a relatively large fellowship to help him fund his studies.[citation needed]

Under Brooks, Morgan completed his thesis work on the embryology of sea spiders—collected during the summers of 1889 and 1890 at the Marine Biological Laboratory in Woods Hole, Massachusetts—to determine their phylogenetic relationship with other arthropods. He concluded that with respect to embryology they were more closely related to spiders than crustaceans. Based on the publication of this work Morgan was awarded his Ph.D. from Johns Hopkins in 1890, and was also awarded the Bruce Fellowship in Research. With the fellowship he was able to travel to Jamaica, the Bahamas and to Europe to conduct further research.[6]

Bryn Mawr

In 1891, Morgan was appointed associate professor (and head of the biology department) at Johns Hopkins' sister school Bryn Mawr College, replacing his colleague E. B. Wilson. Morgan taught all morphology-related courses, while the other member of the department, Jacques Loeb, taught the physiological courses; though Loeb only stayed for one year, it was the beginning of a lifelong friendship.[7] Morgan lectured in biology 5 days a week, giving two lectures a day. He frequently included his own recent research in his lectures, and although he was an enthusiastic teacher, his true interests were in the laboratory. During the first few years at Bryn Mawr he produced descriptive studies of sea acorns, ascidian worms and frogs.

The Stazione Zoologica in Naples, where Morgan studied ctenophore embryology

In 1894 Morgan was granted a year's absence to conduct research in the laboratories of Stazione Zoologica in Naples, where Wilson had worked two years earlier. At the laboratory in Naples he worked with German biologist Hans Driesch, whose research in the experimental study of development piqued Morgan's interest. Among other projects that year, Morgan completed an experimental study of ctenophore embryology. From his exposure in Naples and through Loeb to the Entwicklungsmechanik (roughly, "developmental mechanics") school of experimental biology—a reaction to the vitalistic Naturphilosophie that was exteremly influential in 19th century morphology—Morgan's work shifted from traditional, largely descriptive morphology to an experimental embryology that sought physical and chemical explanations for organismal development.[8]

At the time there was considerable scientific debate over the question of how an embryo developed. Following Wilhelm Roux's mosaic theory of development, some believed that hereditary material was divided among embryonic cells, which were then predestined to form particular parts of a mature organism. Driesch and others thought that development was due to epigenetic factors where interactions between the protoplasam and the nucleus of the egg and the environment could affect development. Morgan was in the latter camp; his work with Driesch demonstrated that blastomeres isolated from sea urchin and ctenophore eggs could develop into complete larvae, contrary to the predictions (and experimental evidence) of Roux's supporters.[9] A related debate involved the role of epigenetic and environmental factors in development; on this front Morgan showed that sea urchin eggs could be induced to divide without fertilization by adding magnesium chloride, work which was continued by Jacques Loeb (who became well known for creating fatherless frogs using the method).[10] [11]

Morgan returned to Bryn Mawr in 1895 and was promoted to full professor. Morgan's main lines of experimental work involved regeneration and larval development; in each case, his goal was to distinguish internal and external causes to shed light on the Roux-Driesch debate. He wrote his first book, The Development of the Frog's Egg, published in 1897. He began a series of studies on different organisms ability to regenerate. He looked at grafting and regeneration in tadpoles, fish and earthworms and in 1901 this work was published as Regeneration. Beginning in 1900, he started working on the problem of sex determination; he was also continued to study the evolutionary problems that had been the focus of his earliest work.[12]

On June 4, 1904, Morgan married Lilian Vaughan Sampson (1870-1952), who had entered graduate school in biology at Bryn Mawr the same year Morgan joined the faculty; she put aside her scientific work in the early years of their marriage, but would later contribute significantly to Morgan's Drosophila work. Later in 1904, E. B. Wilson—still blazing the path for his younger friend—invited Morgan to join him at Columbia University, which at last freed him to focus fully on experimental work.[13]
One of their four children (one boy and three girls) was Isabel Morgan (1911–1996) (marr. Mountain), who became a virologist at Johns Hopkins, specializing in polio research.

Columbia University

In a typical Drosophila genetics experiment male and female flies with known phenotypes are put in a jar to mate; females must be virgins. Eggs are laid in porridge that the larva will feed on; when the life cycle is complete the progeny are scored for inheritance of the trait of interest.

By 1904, when Morgan took a professorship in experimental zoology at Columbia University, he was becoming increasingly focused on the mechanisms of heredity and evolution. The previous year, he had published Evolution and Adaptation; like many biologists at that time, he saw clear evidence for biological evolution (as in the common descent of similar species) but rejected Darwin's proposed mechanism of natural selection acting on small, constantly-produced variations. Extensive work in biometry seemed to indicate that continuous natural variation had distinct limits and did not represent heritable changes. Embryological development posed an additional problem in Morgan's view, as selection could not act on the early, incomplete stages of highly complex organs such as the eye. The common solution of the Larmarckian mechanism of inheritance of acquired characters, which featured prominently in Darwin's theory, was increasingly rejected by biologists. According to Morgan's biographer Garland Allen, he was also hindered by his views on taxonomy: he thought that species were entirely artificial creations that distorted the continuously variable range of real forms, while he held a "typological" view of larger taxa and could see no way that one such group could transform into another. But while he would remain skeptical of natural selection for many years, his theories of heredity and variation were radically transformed through his conversion to Mendelism.[14]

In 1900 three scientists, Carl Correns, Erich von Tschermak and Hugo De Vries had rediscovered the work of Gregor Mendel, and with it the foundation of genetics. De Vries had gone on to propose that new species are created by mutation, bypassing the need for either Lamarckism or Darwinism. Morgan dismissed both of these evolutionary theories, and was actually seeking to prove Hugo De Vries' mutation theory with his experimental heredity work. He was initially quite skeptical of Mendel's laws of heredity (as well as the related chromosomal theory of sex determination), which were being considered as a possible basis for natural selection.

Sex linked inheritance of the white eyed mutation.

Following C. W. Woodworth and William E. Castle, around 1908 Morgan started working on the fruit fly Drosophila melanogaster, and encouraging students to do so as well. With Fernandus Payne, he mutated Drosophila through physical, chemical, and radiational means, and began cross-breeding experiments to find heritable mutations. However, they had no significant success for two years.[15] Castle had also had difficulty identifying mutations in Drosophila, hardly unusual given the flies' tiny size. Finally in 1909, a series of heritable mutants appeared, some of which displayed Mendelian inheritance patterns; in 1910 Morgan noticed a white-eyed mutant male among the red-eyed wild types. When white-eyed flies were bred with a red-eyed female, their progeny were all red-eyed, while a second generation cross produced white-eyed males—a sex-linked recessive trait, the gene for which Morgan named white. Morgan also discovered a pink-eyed mutant that showed a different pattern of inheritance. In a paper published in Science in 1911, he concluded that (1) some traits were sex-linked, (2) the trait was probably carried on one of the sex chromosomes, and (3) other genes were probably carried on specific chromosomes as well.

Morgan's illustration of crossing over, from his 1916 A Critique of the Theory of Evolution

Morgan and his students became more successful at finding mutant flies; they counted the mutant characteristics of thousands of fruit flies and studied their inheritance. As they accumulated multiple mutants, they combined them to study more complex inheritance patterns. The observation of a miniature wing mutant which was also on the sex chromosome but sometimes sorted independently to the white eye mutation, led Morgan to the idea of genetic linkage and to hypothesize the phenomenon of crossing over.He relied on the discovery of the Belgian Professor Frans Alfons Janssens of the University of Leuven who described the phenomenon in 1909 and had called it 'chiasmatypie'. Morgan proposed that the amount of crossing over between linked genes differs and that crossover frequency might indicate the distance separating genes on the chromosome; later English geneticist J. B. S. Haldane suggested that the unit of measurement for linkage be called the morgan. Morgan's student Alfred Sturtevant developed the first genetic map in 1913.

  • The chromosome theory

In 1915 Morgan, Sturtevant, Calvin Bridges and H. J. Muller wrote the seminal book The Mechanism of Mendelian Heredity[16]. Geneticist Curt Stern called the book "the fundamental textbook of the new genetics" and C. H. Waddington noted that "Morgan's theory of the chromosome represents a great leap of imagination comparable with Galileo or Newton".[citation needed] In the following years, most biologists came to accept the Mendelian-chromosome theory, which was independently proposed by Walter Sutton and Theodor Boveri in 1902/1903 and elaborated and expanded by Morgan and his students. Garland Allen characterized the post-1915 period as one of normal science, in which "The activities of 'geneticists' were aimed at further elucidation of the details and implications of the Mendelian-chromosome theory developed between 1910 and 1915." However, the details of the increasingly complex theory, as well as the very concept of the gene and its physical nature, were still controversial. Critics such as W. E. Castle pointed to contrary results in other organisms suggesting that genes interact with each other, while to Richard Goldschmidt and others, there was no compelling reason to view genes as discrete units residing on chromosomes.[17]

Because of Morgan's dramatic success with Drosophila, many other labs throughout the world took up fruit fly genetics. Columbia became the center of an informal exchange network, through which promising mutant Drosophila strains were transferred from lab to lab; Drosophila became one of the first, and for some time the most widely used, model organisms.[18] Morgan's group remained highly productive, but Morgan largely withdrew from doing fly work himself and gave his lab members considerable freedom in designing and carrying out their own experiments. Instead, Morgan returned to embryology and worked to encourage the spread of genetics research to other organisms and the spread of the mechanistic experimental approach (Enwicklungsmechanik) to all biological fields.[19] After 1915, he also became a strong critic of the growing eugenics movement, which frequently co-opted the ideas of genetics in support of racism and worse.[20]

John Hopkins awarded Morgan an honorary LL.D. and the University of Kentucky awarded him an honorary Ph.D. He was elected a member of the National Academy of Sciences and made a foreign member of the Royal Society. In 1924 Morgan received the Darwin Medal. His fly-room at Columbia became world famous and he found it easy to attract funding and visiting academics. In 1927 after 25 years at Columbia, and nearing the age of retirement he received an offer from George Ellery Hale to establish a school of biology in California.

Caltech

Morgan moved to California to head the Division of Biology at the California Institute of Technology in 1928. In establishing the biology division, Morgan wanted to distinguish his program from those offered by Johns Hopkins and Columbia, with research focused on genetics and evolution; experimental embryology; physiology; biophysics and biochemistry. He was also instrumental in the establishment of the Marine Laboratory on Corona del Mar. He wanted to attract the best people to the Division at Caltech, so he took Bridges, Sturtevant, Jack Shultz and Albert Tyler from Columbia and took on Theodosius Dobzhansky as an international research fellow. More scientists came to work in the Division including George Beadle, Boris Ephrussi, Edward L. Tatum, Linus Pauling, Frits Went, and Sidney W. Fox.

In accordance with his reputation, Morgan held numerous prestigious positions in American science organizations. From 1927 to 1931 Morgan served as the President of the National Academy of Sciences; in 1930 he was the President of the American Association for the Advancement of Science; and in 1932 he chaired the Sixth International Congress of Genetics in Ithaca, New York. In 1933 Morgan was awarded the Nobel Prize in Physiology or Medicine; he had been nominated in 1919 and 1930 for the same work. As an acknowledgement of the group nature of his discovery he gave his prize money to Bridges', Sturtevant's and his own children. Morgan declined to attend the awards ceremony in 1933, instead attending in 1934. The 1933 rediscovery of the giant polytene chromosomes in the salivary gland of Drosophila may have influenced his choice. Until that point, the lab's results had been inferred from phenotypic results, the visible polytene chromosome enabled them to confirm their results on a physical basis. Morgan's Nobel acceptance speech entitled "The Contribution of Genetics to Physiology and Medicine" downplayed the contribution genetics could make to medicine beyond genetic counselling. In 1939 he was awarded the Copley Medal by the Royal Society.

He received two extensions of his contract at Caltech, but eventually retired in 1942, becoming professor and chairman emeritus. George Beadle returned to Caltech to replace Morgan as chairman of the department in 1946. Although he had retired, Morgan kept offices across the road from the Division and continued laboratory work. In his retirement he returned to the questions of sexual differentiation, regeneration, and embryology. Morgan had throughout his life suffered with a chronic duodenal ulcer, and in 1945 he experienced a severe heart attack and died from a ruptured artery.

Morgan and Evolution

Morgan was interested in evolution throughout his life. He wrote his thesis on the phylogeny of sea spiders (pycnogonids) and wrote 4 books about evolution. The reason he was interested in evolution is that only characters that are inherited can have an effect in evolution. However, in Evolution and Adaptation (1903) he argued the anti-Darwinist position that selection never could produce wholly new species by acting on slight individual differences[21]. Morgan was not the only scientist attacking natural selection. The period 1875 - 1925 has been called 'The eclipse of Darwinism'[22]. After discovering many small stable heritable mutations in Drosophila he gradually changed his mind. Since Morgan (1915) 'solved the problem of heredity', he was in a unique position to examine critically Darwin's theory of natural selection. In A Critique of the Theory of Evolution (1916) he discussed questions such as: Does selection play any role in evolution? How can selection produce anything new? Is selection no more than the elimination of the unfit? Is selection a creative force? After eliminating some misunderstandings and explaining in detail the new science of Mendelian heredity and its chromosomal basis, Morgan concludes that "the evidence shows clearly that the characters of wild animals and plants, as well as those of domesticated races, are inherited both in the wild and in domesticated forms according to the Mendel's Law". "Evolution has taken place by the incorporation into the race of those mutations that are beneficial to the life and reproduction of the organism".[23]. Injurious mutations have practically no chance of becoming established[24]. Far from rejecting evolution as the title of his 1916 book may suggest, Morgan not only laid the foundation of the science of genetics, but by doing that, he also laid the theoretical foundation for the mechanism of evolution: natural selection. Heredity was a central plank of Darwin's theory of natural selection, but Darwin had a wrong theory of heredity. Therefore, Darwinism could not progress without a correct theory of genetics. Morgan created that foundation. That's why Morgan's work is so important for the neo-Darwinian synthesis despite his criticism at the beginning of his career. Even so, much work remained to be done.

Legacy

Morgan left an important legacy in genetics. Some of Morgan's students from Columbia and Caltech went on to win their own Nobel Prizes, including George Wells Beadle and Hermann Joseph Muller. Nobel prize winner Eric Kandel has written of Morgan, "Much as Darwin's insights into the evolution of animal species first gave coherence to nineteenth-century biology as a descriptive science, Morgan's findings about genes and their location on chromosomes helped transform biology into an experimental science."[25]

The Thomas Hunt Morgan School of Biological Sciences at the University of Kentucky is named for Morgan. In Morgan's honor, the Genetics Society of America annually awards the Thomas Hunt Morgan Medal to one of its members who has made a significant contribution to the science of genetics.

Thomas Hunt Morgan's discovery was illustrated on a 1989 stamp issued in Sweden, showing the discoveries of eight Nobel Prize winning geneticists.

A junior high school in Shoreline, Washington was named in Morgan's honor for the latter half of the 20th century.


See also

References

  1. ^ "The Nobel Prize in Physiology or Medicine 1933". http://nobelprize.org/nobel_prizes/medicine/laureates/1933/index.html. 
  2. ^ List of books by Thomas Hunt Morgan
  3. ^ Fisher, Ronald A. and G. R. de Beer (1947). "Bibliography of Thomas Hunt Morgan". Obituary Notices of Fellows of the Royal Society: 455–466. http://links.jstor.org/sici?sici=1479-571X%28194702%295%3A15%3C451%3ATHM1%3E2.0.CO%3B2-B. 
  4. ^ a b Sturtevant (1959), p283.
  5. ^ Allen (1978), pp11-14, 24.
  6. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 46-51
  7. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 50-53
  8. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 55-59, 72-80
  9. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 55-59, 80-82
  10. ^ Loeb, Jacques (1899). "On the Nature of the Process of Fertilization and the Artificial Production of Normal Larvae (Plutei) from the Unfertilized Eggs of the Sea Urchin". American Journal of Physiology 31: 135–138. http://www.stanford.edu/group/Urchin/loeb.htm. 
  11. ^ Loeb, Jacques (1913). Artificial parthenogenesis and fertilization. University of Chicago Press. http://books.google.com/books?id=6Ct6_1MGe9oC&dq=jacques+loeb+sea+urchin. 
  12. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 84-96
  13. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 68-70
  14. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 105-116
  15. ^ Kohler, Lords of the Fly, pp 37-43
  16. ^ Morgan, Thomas Hunt; Alfred H. Sturtevant, H. J. Muller and C. B. Bridges. The Mechanism of Mendelian Heredity. New York: Henry Holt. http://books.google.com/books?id=GZEEAAAAYAAJ&dq=mechanism+of+mendelian+heredity+morgan. 
  17. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 208-213, 257-278. Quotation from p 213.
  18. ^ Kohler, Lords of the Fly, chapter 5
  19. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 214-215, 285
  20. ^ Allen, Thomas Hunt Morgan: The Man and His Science, pp 227-234
  21. ^ Garland E. Allen in: Michael Ruse & Joseph Travis (2009) Evolution. The First Four Billion Years, Harvard University Press, p.746.
  22. ^ Peter Bowler (2003) Evolution. The History of an Idea, University of California Press, chapter 7.
  23. ^ A Critique of the Theory of Evolution, Princeton University Press, 1916, p. 193-194)
  24. ^ A Critique of the Theory of Evolution, page 189.
  25. ^ Kandel, Eric. 1999. "Genes, Chromosomes, and the Origins of Modern Biology." Columbia Magazine

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