Transposition
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Transcript of Transposition
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Transposition
EvidenceMechanisms:
DNA-mediatedRNA-mediated
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Transposable elements
• Mobile genetic elements - they move from one location in the genome to another
• Found in all organisms (so far studied)• Effects:
– Insertion near or within a gene can inactivate or activate the target gene.
– Cause deletions, inversions, and translocations of DNA
– Lead to chromosome breaks
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Effects of transposable elements depends on their location
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Observations of B. McClintock (1930’s-1950’s)
• Certain crosses in maize resulted in large numbers of mutable loci. – The frequency of change at those loci is much higher
than normally observed.• Studies of these plants revealed a genetic element
called “Dissociation” or Ds on the short arm of chromosome 9.
• Chromosome breaks occurred at the Ds locus, which could be observed cytologically– i.e. by looking at chromosome spreads from individual
cells, e.g. sporocytes.• Frequency and timing of these breaks is controlled
by another locus, called “Activator” or Ac.
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Breaks are visible cytologically on morphologically marked chromosome 9
knob
c sh bz
Wx Ds
wx
C Sh Bz
Heterochromatinbeyond knob
c sh bz
Ds
wx
c sh bz
Ds
wx
2 homologous chromosomes are distinguishable
At pachytene of meiosis, see:
OR
CEN
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McClintock’s chromosome
breaks, 1952
CSHSQB
Chromosome 9, short arm, pachytene phaseof meiosis
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Ds activity can appear at new locations on chromosome 9
knob Wx DsSh Bz
knob WxDsSh Bz
knob WxDs
Sh Bz
knob WxDs
Sh Bz
I
I
I
I
Can find transpositions in the progeny
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Appearance of Ds at a new location is associated with breaks: e.g. Duplications and Inversions
knob Wx DsSh BzI
Wx DsSh BzI
WxDs Sh BzI
DsWx Bz Sh inversion
WxSh BzIDs duplication
OR
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In the presence of Ac,Ds events lead to variegation in sectors of kernels
I
sh bz
Wx Ds
wxC
Sh Bz
sh bz
Ds
wx
After breakage and loss of acentric chromosomes, “recessive” markers are revealed in sectors of kernels.
CEN
Ac
C
C = Colored
I>C, colorless
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Variegation in sectors of kernels
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Variegation in wild flox
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Mechanisms of Transposition
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Flanking direct repeats are generated by insertions at staggered breaks
Flanking direct repeats are generated by insertions at staggered breaks
GTTC
CAAG
5'
3'
Staggered break at the target
GTTC
CAAG
5'
3'
Insert transposable element
CAAG
5'
3'
GTTC
TE
GTTC
CAAG
FDRFDR
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Transposable elements that move via DNA intermediates
• Bacterial insertion sequences– Inverted repeat at ends– Encode a transposase
• Bacterial transposons:– Inverted repeat at ends– Encode a transposase– Encode a drug resistance marker or other
marker– TnA family: transposase plus resolvase
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IS elements and
transposons
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Ac/Ds transposons in maize
• Ac is autonomous– Inverted repeats– Encodes a transposase
• Ds is nonautonomous– Inverted repeats– Transposase gene is defective because of
deletions in coding region
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Structure of Ac and Ds
transposase
CAGGATGAAA TTTCATCCCTA
Ac
Ds
CAGGATGAAA TTTCATCCCTA
Nonfunctional transposase
deletion
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Replicative vs. Nonreplicative transposition
TE
Replicon A with a transposable element = TE
Relicon B
TE
TE
TE TE
Replicative transposition:
+ +
Cointegrate
fusion of repliconsduring replicationof the TE
recombination
Nonreplicative transposition
TE
+
TE
+
Donor Recipient Donor replicon islost unless the breakis repaired.
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Mechanism for DNA-mediated transposition
• Transposase nicks at ends of transposon (note cleavage is at the same sequence, since the ends are inverted repeats).
• Transposase also cuts the target to generate 5’ overhangs• The 3’ end of each strand of the transposon is ligated to the 5’
overhang of the target site, forming a crossover structure.
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Crossover intermediate in transposition
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Replicative transposition from the crossover structure
• The 3’ ends of each strand from the staggered break (at the target) serve as primers for repair synthesis.
• Copying through the transposon followed by ligation leads to formation of a cointegrate structure.
• Copying also generates the flanking direct repeats.• The cointegrate is resolved by recombination.
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Nonreplicative transposition from the crossover structure
• Crossover structure is released by nicking at the other ends of the transposon (i.e. the ones not initially nicked).
• The gap at the target (now containing the transposon) is repaired to generate flanking direct repeats.
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3-D structure of transposase and Tn5 DNA end
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Transposition into a 2nd site on the same DNA molecule
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Almost all transposable elements in mammals fall into one of four classes
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Transposable elements that move by RNA intermediates
• Called retrotransposons• Common in eukaryotic organisms
– Some have long terminal repeats (LTRs) that regulate expression
• Yeast Ty-1• Retroviral proviruses in vertebrates
– Non-LTR retrotransposons• Mammalian LINE repeats ( long interspersed repetitive
elements, L1s)• Similar elements are found even in fungi• Mammalian SINE repeats (short interspersed repetitive
elements, e.g. human Alu repeats)• Drosophila jockey repeats• Processed genes (have lost their introns). Many are
pseudogenes.
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Age distri-bution
of repeats
in human
and mouse
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Mechanism of retrotransposition
• The RNA encoded by the retrotransposon is copied by reverse transcriptase into DNA
• Primer for this synthesis can be generated by endonucleolytic cleavage at the target
• Both reverse transcriptase and endonuclease are encoded by SOME (not all) retrotransposons
• The 3’ end of the DNA strand at the target that is not used for priming reverse transcriptase can be used to prime 2nd strand synthesis
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Events in L1 transposition
ORF1
ORF2RT’aseendonuclease
3’ UTRpromoter
FDR FDR
transcribe
Staggered break at target
Priming of synthesis by RT’ase at staggered breakPriming of synthesis by RT’ase at staggered break
2nd strand synthesis and repair of staggered break
RT’ase works preferentially on L1 mRNA
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Recombination between two nearly identical sequences (e.g transposons) will lead to
rearrangements
• Deletion if the repeats are in the same orientation
• Inversion if the repeats are in the opposite orientation
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Consequences of
recombination between two transposons