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The lines go side by side on the same tower only for part of their length, and despite the fact that their transposition has been performed, the currents in both lines are also unbalanced.
TEs are generally classified according to their transposition mechanism.
This is believed to suppress most of their transposition activity [9], [10].
Several DNA transposons in newly synthesized Arabidopsis allopolyploids, also display transcriptional activity, although their transposition is limited [34].
SINEs are too small to harbor a coding function, and for their transposition they use reverse transcriptases encoded by LINEs.
These ISs use REPs as targets for their transposition.
TEs are classified into two classes based on their transposition mechanism.
ATons lack protein coding capacity and their transposition is dependent on transposases produced by autonomous elements.
These changes lead to the expression of RTEs, culminating in their transposition.
Their transposition mechanism leads to 5' end truncations of the new inserted sequence.
Full length LTR elements store information of their transposition history in the LTRs [ 22, 23].
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