Patching gaps in plant genomes results in gene movement and erosion of colinearity

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Figure 4.
Figure 4.

Molecular signatures that point to DSB repair as the cause of gene movement. (Red) Target site duplications (TSDs) that were produced upon the insertion of transposable elements; (gray) mismatches. The double-strand break (DSB) induced by the transposable element insertion occurred within a few base pairs of the terminus of the transposable element. A model for the molecular events that led to the situation in A is given in Figure 6. Depending on the precise location of the DSB, TSDs are flanking the transposable element (CE), the duplicated region (B,F), or both (A). The example in C is flanked on one side by an array of direct repeats. It is possible that a combination of the TE insertion and the presence of the repeat array lead to the DSB (see also Fig. 5).

This Article

  1. Genome Res. 20: 1229-1237

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