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. Author manuscript; available in PMC: 2011 May 1.
Published in final edited form as: Mech Dev. 2010 Mar 27;127(5-6):265–280. doi: 10.1016/j.mod.2010.03.003

Fig. 5.

Fig. 5

Two Dys:Tgo sites and Motif 1 sites are required for fusion cell transcription of CG13196. (A) Schematic of the 3.3 kb genomic region encompassing the CG13196 gene, and fragments analyzed in vivo. Shown are the three TCGTG sequences, two Motif 1 sequences, and an AAG sequence adjacent to TCGTG-C. (B–D) The C350 and D92 fragments drove GFP expression in all fusion cells, whereas fusion cell expression was absent in the B490 transgenic strain. (E–Y) Shown are DT fusion cells for (E–G) unaltered and (H–Y) altered versions of D92. Both (H–M) deletion and (N–S) mutation of each TCGTG site abolished fusion cell expression. Deletion of Motif 1 sites also abolished expression (T–V), whereas deletion of the AAG sequence adjacent to TCGTG-C had no effect (W–Y).