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HIV LTR editing with mRNAs of TAR TALENs.

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posted on 2015-03-17, 04:09 authored by Hirotaka Ebina, Yuka Kanemura, Naoko Misawa, Tetsushi Sakuma, Tomoko Kobayashi, Takashi Yamamoto, Yoshio Koyanagi

(A) Kinetics of GFP transduction with mRNA and plasmid DNA in Jurkat cells. Jurkat cells were transfected with 1 μg of mRNA GFP or 1 μg of plasmid GFP under the control of a CMV promoter. The time course analysis of GFP expression was performed by flow cytometry. (B and C) A Jurkat cell line latently transduced with an LTIG vector was transfected with mTALENs. The level of GFP expression 48 hours after TNF-α stimulation is shown. Representative histograms are shown in B. The positive percentage of GFP is shown in B (n = 3). (D and E) ACH-2 cells were transfected with TAR mTALENs. The expression of p24 antigen 48 hours after TNF-α stimulation is shown. The percentage of p24 antigen expression in cells is shown in C (n = 3). The amount of p24 antigen in the culture supernatant is shown in E (n = 3). The error bars in A, C, D, and E show standard deviations (n = 3).

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