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. 2016 May 16;11(5):e0155578. doi: 10.1371/journal.pone.0155578

Fig 5. A region spanning the first 100 nucleotides of mpc is involved in the expression regulation of the downstream genes within lee3.

Fig 5

(A) An illustration of the constructs carrying an expression cassette similar to that of pV-N except that differently sized regions from the 3’-end of mpc are separately placed upstream to escV. (B) Western blotting analysis using anti-Hisx6 is able to detect the amount of tagged EscN expressed by the individual constructs. Note: a dot-framed mpc fragment represents the 3’-end remaining mpc sequence that has been introduced without an in-frame ATG. The number above each frame represents the size (in base pairs) of the 3’-end fragment of mpc. The 5’-end nucleotides of mpc truncated are superscripted with “Δ.” A solid-line frame indicates that an ATG has been in-frame engineered in front of the mpc fragment containing nucleotides 52–354. Note: mpcΔ51–100 represents a deletion of nucleotides 51–100 of mpc in the construct, and this construct contains no in-frame ATG since the first 50 nucleotides of the frame was derived from ACmpc. See legend to Fig 1 for additional explanations of the diagram.