Department of Molecular Cellular and Developmental Biology, Yale University, 219 Prospect Street, New Haven, CT, 06511, USA.
Systems Biology Institute, Yale University, 850 West Campus Drive, West Haven, CT, 06516, USA.
Nat Commun. 2023 Nov 27;14(1):7719. doi: 10.1038/s41467-023-43233-y.
Application of microfluidic platforms facilitated high-precision measurements of yeast replicative lifespan (RLS); however, comparative quantification of lifespan across strain libraries has been missing. Here we microfluidically measure the RLS of 307 yeast strains, each deleted for a single gene. Despite previous reports of extended lifespan in these strains, we found that 56% of them did not actually live longer than the wild-type; while the remaining 44% showed extended lifespans, the degree of extension was often different from what was previously reported. Deletion of SIS2 gene led to the largest RLS increase observed. Sis2 regulated yeast lifespan in a dose-dependent manner, implying a role for the coenzyme A biosynthesis pathway in lifespan regulation. Introduction of the human PPCDC gene in the sis2Δ background neutralized the lifespan extension. RNA-seq experiments revealed transcriptional increases in cell-cycle machinery components in sis2Δ background. High-precision lifespan measurement will be essential to elucidate the gene network governing lifespan.
微流控平台在酵母复制寿命(RLS)的高精度测量中得到了广泛应用;然而,不同菌株库之间的寿命比较定量分析仍然缺乏。在这里,我们通过微流控技术测量了 307 株酵母菌株的 RLS,这些菌株都缺失了单个基因。尽管之前有报道称这些菌株的寿命延长,但我们发现其中 56%的菌株实际上并没有比野生型菌株活得更长;而剩下的 44%菌株显示出延长的寿命,但延长的程度往往与之前的报道不同。SIS2 基因的缺失导致了观察到的最大 RLS 增加。Sis2 以剂量依赖的方式调节酵母寿命,暗示辅酶 A 生物合成途径在寿命调节中的作用。在 sis2Δ 背景中引入人 PPCDC 基因使寿命延长得到了中和。RNA-seq 实验揭示了 sis2Δ 背景中细胞周期机制成分的转录增加。高精度寿命测量对于阐明调控寿命的基因网络至关重要。