Department of Biology, Harvey Mudd College, Claremont, CA, 91711, USA.
Department of Integrative Biology and Physiology, University of California, Los Angeles, CA, 90095, USA.
Sci Rep. 2019 Feb 28;9(1):3170. doi: 10.1038/s41598-019-39508-4.
The β5 subunit of the proteasome has been shown in worms and in human cell lines to be regulatory. In these models, β5 overexpression results in upregulation of the entire proteasome complex which is sufficient to increase proteotoxic stress resistance, improve metabolic parameters, and increase longevity. However, fundamental questions remain unanswered, including the temporal requirements for β5 overexpression and whether β5 overexpression can extend lifespan in other species. To determine if adult-only overexpression of the β5 subunit can increase proteasome activity in a different model, we characterized phenotypes associated with β5 overexpression in Drosophila melanogaster adults. We find that adult-only overexpression of the β5 subunit does not result in transcriptional upregulation of the other subunits of the proteasome as they do in nematodes and human cell culture. Despite this lack of a regulatory role, boosting β5 expression increases the chymotrypsin-like activity associated with the proteasome, reduces both the size and number of ubiquitinated protein aggregates in aged flies, and increases longevity. Surprisingly, these phenotypes were not associated with increased resistance to acute proteotoxic insults or improved metabolic parameters.
蛋白酶体的β5 亚基已在蠕虫和人类细胞系中被证明具有调节作用。在这些模型中,β5 的过表达导致整个蛋白酶体复合物的上调,这足以增加蛋白毒性应激抗性、改善代谢参数并延长寿命。然而,仍有一些基本问题尚未得到解答,包括β5 过表达的时间要求,以及β5 过表达是否可以延长其他物种的寿命。为了确定β5 亚基在成年期的过表达是否可以在另一种模型中增加蛋白酶体的活性,我们研究了β5 过表达在黑腹果蝇成年期的表型。我们发现,β5 亚基的成年期过表达不会像在线虫和人类细胞培养物中那样导致蛋白酶体其他亚基的转录上调。尽管缺乏调节作用,但提高β5 的表达水平会增加与蛋白酶体相关的糜蛋白酶样活性,减少老年果蝇中泛素化蛋白聚集体的大小和数量,并延长寿命。令人惊讶的是,这些表型与急性蛋白毒性应激的抗性增加或代谢参数的改善无关。