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Genetic recombination.pptx

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Dna recombinant technology
Dna recombinant technology
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Genetic recombination.pptx

  1. 1. Genetic recombination Harish. R Assistant Professor Department of Biosciences, Mar Thoma College, Thiruvalla hareesh@marthomacollege.org
  2. 2. 1. General or homologous recombination : occurs between DNA molecules of very similar sequence, such as homologous chromosomes in diploid organisms. Is an integral part of the complex process of meiosis in sexually reproducing organisms. Results in crossing over. In Bacteria: recombination during F-factor mediated conjugal transfer of parts of chromosomes. In Bacteriophages Recombination between two phage during a mixed infection of bacteria  Breaking and rejoining of two parental DNA molecules to produce new DNA molecules Genetic recombination
  3. 3. 2. Illegitimate or nonhomologous recombination occurs in regions where no large-scale sequence similarity is apparent, (i.e due to translocations between different chromosomes or deletions that remove several genes along a chromosome). 3. Site-specific recombination occurs between particular short sequences (about 12 to 24 bp) present on otherwise dissimilar parental molecules. Eg. integration of bacteriophages.
  4. 4. 3. Replicative recombination: generates a new copy of a segment of DNA. New DNA molecules carry genetic information from both parental molecules. Ex: transposable elements, Mu Phages.
  5. 5. Mechanism of Recombination • Endonuclease cuts DNA in the middle of a strand, and nicks one strand of the donor DNA. • This nicked strand is separated from the other strand by proteins with helicase activity • The resulting single-stranded segment binds to SSbps and then RecA. This results in a complex that promotes base pairing with the complementary sequence in the recipient DNA molecule. • This base pairing in turn displaces the other strand of the recipient DNA molecule (strand invasion). • Heteroduplex regions, with each strand originated from a different chromosomes. • Resolvase (RuvC protein): specifically cleave Holliday intermediates have also been isolated from bacteria and yeast. • COMPLEMENTATION
  6. 6. Rec A Protein • A 38 kilodalton protein essential for the repair and maintenance ofDNA. • Activated during DNA Damage • The RecA protein binds strongly to ssDNA to form a nucleoprotein filament. • Has more than one DNA binding site, and thus can hold a both the strands together. • This feature makes it possible to catalyze a DNA synapsis reaction between a DNA double helix and a complementary region of single stranded DNA.
  7. 7. Watson, J.D, Baker T.A, Bell, S.P, Gann, A., Levine, M and Losik R ( 2004). The replication of DNA, Molecular` Biology of the Gene, (5th ed). Perason Education Inc. Ch.8 (181-233). Madigan, M.T, Martinko, J.M, Bender, K.S, Buckley, D.H and Stahl, D.A .(2015). Molecular Microbiology. Brock Biology of Microorganisms.(14thed) Perason Education Inc. Ch.4 (107-135). Madigan, M.T, Martinko, J.M, Bender, K.S, Buckley, D.H and Stahl, D.A .(2015). Genetics of Bacteria and Archaea. Brock Biology of Microorganisms. .(14thed) Perason Education Inc. Ch.10(291-301) Watson, J.D, Baker T.A, Bell, S.P, Gann, A., Levine, M and Losik R ( 2004). The Mutability and Repair of DNA, Molecular` Biology of the Gene (5th ed) , Perason Education Inc. Ch.9 (235-258). Weaver. R.F (2002) The Transcription Apparatus of Prokaryotes. Molecular Biology (2nd ed). The McGraw−Hill Ch.6 (139-266) Weaver. R.F (2002) DNA Replication I: Basic Mechanism and Enzymology. Molecular Biology (2nd ed). The McGraw−Hill Ch.20 (648-790) References
  8. 8. Dale, J.W and Park S.F (2004). Nucleic Acid Structure and Function, Molecular Genetics of Bacteria (4th ed). John Wiley & Sons. Ch.1 (1- 33). Dale, J.W and Park S.F (2004). Mutation and Variiation, Molecular Genetics of Bacteria (4th ed). John Wiley & Sons. Ch.2 (37-62). Dale, J.W and Park S.F (2004). Gene Transfer, Molecular Genetics of Bacteria (4th ed). John Wiley & Sons. Ch.6 (165-187) References

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