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. Author manuscript; available in PMC: 2014 Dec 15.
Published in final edited form as: Cell Rep. 2014 Oct 23;9(3):1135–1150. doi: 10.1016/j.celrep.2014.09.042

Figure 3. Functional Chaperome Perturbation Analyses in C.elegans Models of Protein Misfolding.

Figure 3

A. The C. elegans Chaperome with its functional families and numbers of members per family are shown. B. Paralysis (% motility) for wild type and Aβ42 expressing C. elegans from day 1 to day 12 of adulthood. Arrow indicates paralysis age-of-onset. C. Motility defects for wild type and Q35-expressing C. elegans from day 1 to day 12. Arrow indicates age-of-onset. D. RNAi paralysis phenotypes on day 4 of adulthood (% motility) for C. elegans expressing Aβ42 (Mean ± SEM, n=3 and n ≥ 25 animals/trial). E. RNAi motility defects on day 2 of adulthood (% motility) for C. elegans expressing Q35 (Mean ± SEM, n=3 and n ≥ 25 animals/trial). F. Venn diagram indicating significant overlap of 16 hits from both screens (P < 2.2e-16, Fisher's exact test). G. Average paralysis (% motility) for RNAi of all 16 chaperome subset genes in Aβ42 expressing C. elegans throughout adulthood (days 1 to 12). Data points are means of corresponding data points in each RNAi experiment, each based on n ≥ 3 independent experiments and n ≥ 25 animals/trial. ** P < 0.01, Student's t-test. H. Average paralysis (% motility) for chaperome subset RNAi in Q35 expressing C. elegans throughout adulthood (days 1 to 12). Data points as in G. (See Figure S4).