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Fig. 2

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ZDB-IMAGE-200310-6
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Figures for Perenthaler et al., 2019
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Fig. 2

UGP2 homozygous variant leads to a loss of the shorter protein isoform in patient fibroblasts. a Schematic drawing of the human UGP2 locus, with both long and short transcript isoforms. Boxes represent exons, with coding sequences indicated in green. The location of the recurrent mutation is indicated in both transcripts. b Western blotting of cellular extracts derived from control fibroblasts and fibroblasts obtained from family 1, detecting the housekeeping control vinculin and UGP2. Note the two separated isoforms of UGP2 that have a similar intensity in wild-type cells. The shorter isoform is less expressed in fibroblasts from heterozygous parents and absent in fibroblasts from the affected proband. c Western blot quantification of the fraction of short UGP2 protein isoform compared to total UGP2 expression in control, parental heterozygous and proband homozygous fibroblasts, as determined in three independent experiments. Error bars represent SEM. d Western blot quantification of total UGP2 protein levels, as determined by the relative expression to the housekeeping control vinculin. Bar plot showing the results from three independent experiments. Error bars represent SEM; no significant differences were found between parents and proband, t test, two tailed. e Cell proliferation experiment of fibroblasts from heterozygous parents and homozygous proband from family 1, during a 5-day period, determined in three independent experiments. Error bars represent SEM. f Immunocytochemistry on cultured control and UGP2 heterozygous and homozygous mutant fibroblasts derived from family 1, detecting UGP2 (red). Nuclei are stained with DAPI. Scale bar 50 µm. g Enzymatic activity of UGP2 in control and UGP2 heterozygous and homozygous mutant fibroblasts derived from family 1. Shown is the mean of two independent experiments. Error bars represent SEM; no significant differences were found, unpaired t test, two tailed

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