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. 2019 Jun 20;4(12):e128561. doi: 10.1172/jci.insight.128561

Figure 1. Triobp gene structure, transcripts, protein isoforms, and mutant alleles.

Figure 1

(A) Alternative transcripts of mouse Triobp, the corresponding encoded protein isoforms, and their predicted domains. Locations of the epitopes for 2 antibodies (TRIOBP-4/5 and TRIOBP-5) are depicted with orange and light-blue rectangles, respectively. (B) Drawing of an organ of Corti sensory epithelium segment showing 1 row of inner (IHC) and 3 rows of outer (OHC) hair cells. Inset shows Deiters’ and outer pillar cells supporting an OHC. (C) Mutations of Triobp used to generate 2 genetically different TRIOBP-5–deficient mouse models. TriobpΔEx9-10/ΔEx9-10 has a LacZ cassette replacing exons 9 and 10 of Triobp-5 (schematic 1). The TriobpΔEx8 allele has a LacZ cassette replacing exon 8 (schematic 2) and the TriobpYHB226 allele has a trap cassette with a LacZ insertion in exon 17 (schematic 3). The combination in trans of these 2 Triobp mutations is a compound heterozygote designated TriobpΔEx8/YHB226. Expression of wild-type Triobp isoforms 1, 4, and 5 is indicated to the right of the schematics for each genotype.