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The published data showed that mPing was actively transposed during the processes of the de-differentiation and proliferation [ 13], but whether the re-differentiation could induce MITE transposition is ambiguous.
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pMGB1 carries two dissimilar mobile OrfB elements, of which one was absent from some sequenced clones of pMGB1, suggesting that it was actively transposing.
In this study, we showed that mGing, as a new member of Gaijin family, was actively transposing in rice under stress conditions.
In anther culture experiment, we observed that mPing was actively transposing in all plantlet samples and mGing in about 50% of the samples, but active transposition was not identified in calli for both elements.
mGing is actively transposed under γ-ray irradiation or in cell re-differentiation process in rice.
Recently, a study demonstrated that the Stowaway-like MITEs could also be actively transposed in vitro in a yeast co-transposition system with rice autonomous Mariner-like transposons [ 16].
These alignments suggest that many of the highly represented elements may be actively transposing, despite the diverged nature of many transposable element families.
Furthermore, npiggy1_Mm shows activity patterns suggesting that it may currently still be actively transposing in M. murinus.
However, the Gnome family may still be actively transposing in mosquito populations if intact copies of Ozma are still present.
In this regard, the most valuable TEs are those that are actively transposing and generating insertion site polymorphisms.
Transposition footprints from the rice MITE mPing, the only group of MITEs observed to be actively transposing, have been characterized in several recent studies [ 21- 24].
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