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Overall, our data show that age-dependent protein aggregation is not necessarily caused by increased protein levels. Instead, other events associated with age can promote aggregation.

Protein Insolubility in Young Animals

Whole-protein staining shows that many of the insoluble proteins detected in aged animals are also present in relatively young animals (Day 3 of adulthood at 25°C) at a time when no obvious signs of aging are visible ( Figure 1A ). Similarly, Western blot analysis revealed the presence of KIN-19, DAF-21/HSP90, and PAR-5 in the insoluble fraction from young and animals ( Figure 3 and 9Forty LA Dodgers Adjustable Baseball Cap in Seersucker Blue New Era LiNWBUC3
). In addition, our mass spectrometry analysis showed that the vast majority of both and / age-aggregated proteins were also insoluble to some extent in the young animals ( BOURNE mens cap Conte Of Florence OygFs
). Overall, the presence of insoluble proteins in the younger animals, albeit at relatively low levels, suggests that protein aggregation is not limited to mid-life or old animals but already occurring in healthy young animals. It is conceivable that these insoluble proteins have a function in young adults, but these findings are also consistent with recent reports showing that a decline in proteostasis begins in young animals [40] .

To further evaluate the importance of the aging process in mediating protein aggregation, we asked whether a mutation that slows aging would affect the rate of inherent protein aggregation. Mutation of the daf-2 /insulin/IGF-1-receptor gene doubles the lifespan of C. elegans ACCESSORIES Hats Msgm xCnfTIYZ
and delays proteotoxicity in C. elegans ' disease models of aberrant protein aggregation [42] , Modal Scarf Mango Madness by VIDA VIDA aHsZBPZ2QV
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, [45] , we chose to focus on aggregation in somatic tissues in the gon-2(−) mutants. When daf-2 RNAi treatment is initiated at hatching or at the last larval stage, the animals grow to become long-lived adults [46] . The pattern of insoluble proteins in young-adult animals subjected to daf-2 RNAi (from the first larval stage) resembled that of wild type ( Figure 5A ). However, we found only a slight increase in insolubility with age (1.6-fold) compared to control animals (3.6-fold). More strikingly, the insolubility pattern of proteins extracted from daf-2(RNAi) animals did not change with age, whereas the two patterns (young versus old) were very different in wild type. Exposure to daf-2 RNAi from the last larval stage produced very similar results (unpublished data). Similarly, Western blot analysis showed that daf-2 RNAi treatment greatly reduced the extent of both RHO-1 and DAF-21 insolubility with age and moderately reduced the extent of KIN-19 and PAR-5 age-dependent insolubility ( Leather Passport Case Ho by VIDA VIDA 2UDu7r
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