Horizontal gene transfer in prokaryotes: Difference between revisions

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[[Image:J_Lederberg.jpg|frame|Joshua Lederberg in the 1960s (NLM)]]
[[Image:J_Lederberg.jpg|frame|Joshua Lederberg in the 1960s (NLM)]]


*The discovery of '''horizontal gene transfer''' between different species began in 1946, when [[Joshua Lederberg]] and [[Edward Tatum]] discovered genetic conjugation in ''Escherichia coli'' K-12 <ref>Lederberg, J. and Tatum, E. L. (1946). Novel genotypes in mixed cultures of biochemical mutants of bacteria. Cold Spring Habor Symposia of Quantitative Biology. 11, p113.</ref>, and this process was later shown to be carried out by the first recognized [[plasmid]], fertility factor F. In 1951, Joshua and Ester Lederberg , together with Zinder and Lively report the first evidence of bacterial genetic recombination in ''Salmonella'' that was later shown to be caused by bacteriophage mediated [[transduction]] of bacterial chromosome fragments, which is the term used for horizontal movement of genes carried in bacterial viruses. Joshua Lederberg's discovery of conjugation was famously described by Salvador Luria (1947) as " to be among the most fundamental advances in the whole history of bacteriological science", giving great prominence to studies of horizontal gene transfer during the 1950s, 60s and 70s <ref>Hayes, W. (1970) The Genetics of Bacteria and their Viruses.2nd Edition, Blackwell.</ref>. Transduction is currently recognized as a major route for horizontal gene movement in bacteria, and plasmid mediated [[bacterial conjugation]] is now known to be promiscuous process that enables DNA to transfer across taxonomic species, genera, phyla and domains.
*The discovery of '''horizontal gene transfer''' between different species began in 1946, when [[Joshua Lederberg]] and [[Edward Tatum]] discovered genetic exhange in ''Escherichia coli'' K-12 <ref>Lederberg, J. and Tatum, E. L. (1946). Novel genotypes in mixed cultures of biochemical mutants of bacteria. Cold Spring Habor Symposia of Quantitative Biology. 11, p113.</ref>, and this process was later found out by the recognized [[plasmid]], fertility factor F. In 1951, Joshua and Ester Lederberg , together with Zinder and Lively reported also  the first evidence of genetic recombination in the bacterium ''Salmonella'' that was later shown to be caused by bacterial virus mediated of bacterial chromosome fragments. This came to be called bacteriophage [[transduction]] , which is the term used for horizontal movement of genes carried in bacterial viruses. Joshua Lederberg's discovery of conjugation was famously described by Salvador Luria (1947) as " to be among the most fundamental advances in the whole history of bacteriological science", giving great prominence to studies of horizontal gene transfer during the 1950s, 60s and 70s <ref>Hayes, W. (1970) The Genetics of Bacteria and their Viruses.2nd Edition, Blackwell.</ref>. Transduction is currently recognized as a major route for horizontal gene movement in bacteria, and plasmid mediated [[bacterial conjugation]] is now known to be promiscuous process that enables DNA to transfer across taxonomic species, genera, phyla and domains.


===Plasmids, episomes, mobile DNA in microorganisms===
===Plasmids, episomes, mobile DNA in microorganisms===

Revision as of 02:05, 10 December 2006

Template:Stub Horizontal gene transfer is common among bacteria, even very distantly-related ones. This process is thought to be a significant cause of increased drug resistance; when one bacterial cell acquires resistance, it can quickly transfer the resistance genes to many species. Enteric bacteria appear to exchange genetic material with each other within the gut in which they live. There are three common mechanisms for horizontal gene transfer:

History of horizontal gene transfer in prokaryotes

Joshua Lederberg in the 1960s (NLM)
  • The discovery of horizontal gene transfer between different species began in 1946, when Joshua Lederberg and Edward Tatum discovered genetic exhange in Escherichia coli K-12 [1], and this process was later found out by the recognized plasmid, fertility factor F. In 1951, Joshua and Ester Lederberg , together with Zinder and Lively reported also the first evidence of genetic recombination in the bacterium Salmonella that was later shown to be caused by bacterial virus mediated of bacterial chromosome fragments. This came to be called bacteriophage transduction , which is the term used for horizontal movement of genes carried in bacterial viruses. Joshua Lederberg's discovery of conjugation was famously described by Salvador Luria (1947) as " to be among the most fundamental advances in the whole history of bacteriological science", giving great prominence to studies of horizontal gene transfer during the 1950s, 60s and 70s [2]. Transduction is currently recognized as a major route for horizontal gene movement in bacteria, and plasmid mediated bacterial conjugation is now known to be promiscuous process that enables DNA to transfer across taxonomic species, genera, phyla and domains.

Plasmids, episomes, mobile DNA in microorganisms

  • The existence of several genetic structures that can insert within bacterial chomosomes, based on observation of the bacteriophage lambda and fertility factor in 1958 F lead F. Jacob and E. L. Wollman [3] to coin the term episome for DNA elements that have alternate modes of existence within the cell, either in the chromosome, or as autonomously resplicating stuctures. Subsequent study of these phenomenon revealed numerous occurences of mobile DNA in a wide range of organisms [4](such as the presence of insertion sequence (IS) "jumping genes" that allow F plamid insertion in the chromosome) and widespread horizontal gene transfer involving by bacteriophage, plasmids and mobile DNA in general.
  • Tomoichiro Akiba and Kunitaro Ochia discover mobile antibiotic resistance genes in bacteria [5], and the horizontal transfer is later shown to mediated by plasmids that inject DNA promiscuously into other cells [6].
  • James Shapiro discovers that spontaneously occuring insertions of large inserts of extra DNA can causes mutationss in the galactose genes of the bacterium Escherichia coli [7]. This discovery ultimately led to the discovery of mobile inserton sequences (IS).

References

  1. Lederberg, J. and Tatum, E. L. (1946). Novel genotypes in mixed cultures of biochemical mutants of bacteria. Cold Spring Habor Symposia of Quantitative Biology. 11, p113.
  2. Hayes, W. (1970) The Genetics of Bacteria and their Viruses.2nd Edition, Blackwell.
  3. Jacob, F. and Wollman, E. L. (1958) Les episomes, elements genetiques ajoutes. C. R. Acad, Sci. Paris, 247, p154.
  4. Berg, D. E. and Howe, M. M. (Eds.)(1989). Mobile DNA. American Society for Microbiology. Washington, D.C.
  5. Ochia, K. Yamanaka, T. Kimura, K. and Sawada, O. (1959). Inheritance of drug resistance (and its transfer) between Shigella strains and between Shigella and E. coli strains. Nihon Iji Shimpo 1861: p34 (In Japanese)
  6. S. Falcow (1975)Infectious Multiple Drug Resistance. Pion Press, London.
  7. Shapiro, J. (1969) Mutations caused by the insertion of genetic material into the galactose operon of Escherichia coli. J. Molec. Biol. 40, p93-109.

Further reading

  • Snyder, L. and Champness, W. (2003) Molecular Genetics of Bacteria, @nd Edition, ASM Press Washington DCISBN 1-55581-204-X

External links