Fig. 1: Strategy to insert additional genes into MeV genomes. | npj Vaccines

Fig. 1: Strategy to insert additional genes into MeV genomes.

From: Versatility of live-attenuated measles viruses as platform technology for recombinant vaccines

Fig. 1

a Schematic depiction of the DNA Sequence of the intergenic region between P and M genes of MVNSe revealing insertion of an additional intergenic region (aigr) to be utilized as an additional transcription unit (ATU) to encode extra genes in the genome of recombinant MeV, in this example the HBsAg30. Shown is the sense strand of DNA sequences used for cloning. Open reading frames (ORFs) are depicted by black boxes, recognition sequences for restriction endonucleases are outlined in sequences in italics30 and respective endonucleases are indicated. Conserved transcription termination (lilac) and re-initiation (red) sequences of the MeV polymerase separated by the non-transcribed intergenic triplet CT/GT (blue) are color coded and framed. Bold, stop and start-codons for translation of flanking viral P and M protein ORFs. b Schematic depiction of rec. MeV genomes. Gray boxes indicated MeV ORFs, red arrows positions where ATUs have been inserted and used for the expression of additional transgenes.

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