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Chapter 13: transposable elements
Fig 13-1
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Multiple IS elements can exist at diverse sites
in bacterial chromosomes and plasmids Example: IS elements in an F factor Fig 13-8
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Various classes of Insertion Sequence (IS) elements
have been identified in E. coli Element-specific inverted DNA sequence repeats flank each element
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Transposons may be elaborate IS-type elements (simple)
or DNA fragments with IS elements at each end Fig 13-9
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Individual plasmids can contain multiple transposons
carrying multiple resistance genes Mobility of the transposons provides extensive mobility of the R factors Fig 13-10
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Insertion of a bacterial transposons usually involves
duplication of DNA sequences flanking the insertion site Resembles restriction endonuclease cut Fig 13-11
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Two modes of transposition of a bacterial transposons
Fig 13-12
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Replicative transposition involves cointegrate intermediate
Fig 13-13
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One class of eukaryote transposable elements (retrotransposons)
appear to be related to retroviruses Retrovirus life cycle Fig 13-14
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All contain vestiges of retroviral genes
Examples of eukaryote retrotransposons All contain vestiges of retroviral genes most retain pol Fig 13-15
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Retrotransposons such as yeast Ty1
transpose through an RNA intermediate Fig 13-16
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The first transposon system identified:
Ac-Ds system in corn (B. McClintock) Ac transposase can mobilize more than one transposon Fig 13-21
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Drosophila P elements were discovered
by study of a hybrid dysgenesis syndrome Fig 13-18
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P-M dysgenesis is due to presence of the P element transposon in P flies
Fig 13-19
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P-M dysgenesis is due to presence of the P element transposon in P flies
Fig 13-19 Mobilization limited to germline cells: Normal development of somatic tissue degenerate germ cells due to massive genetic damage Fig 13-20
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P element has been engineered as a transformation vector
Fig 13-22
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Up to ½ of human genome is transposable elements and residues
Fig 13-23
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The human HGO gene contains numerous repetitive elements
All elements are within introns (exon insertions are presumably subject to negative selection) Fig 13-24
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Many mutations are caused by insertions
of transposable genetic elements
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Retrotransposon abundance accounts for enormous differences in genome sizes in different grasses
Fig 13-25
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Some transposons display insertion site specificities
that promote their accumulation in “safe havens” Fig 13-
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Fig 13-
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Fig 13-
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