Transgene designed to study DNA double-strand break repair by single strand annealing (SSA). Consists of MtnB promoter/enhancer sequence upstream of a direct repeat of a 259bp genomic fragment of the MtnB transcription unit (this repeat includes MtnB UTR and coding sequence) in which the two repeats are separated by a RS(I-SceI) site, and with EGFP fused downstream of the second repeat. A silent point mutation has been introduced into both of the direct repeats (so that they are identical). In this configuration, the EGFP protein is not expressed. EGFP protein is only expressed if a double-strand DNA break is induced at the RS(I-SceI) site by the I-SceI endonuclease, and the break is repaired by single strand annealing (SSA) of the flanking MtnB direct repeats.