Ypt4 and lvs1 regulate vacuolar size and function in Schizosaccharomyces pombe.

Cellular logistics Pub Date : 2017-06-09 eCollection Date: 2017-01-01 DOI:10.1080/21592799.2017.1335270
Addison Rains, Yorisha Bryant, Kaitlyn A Dorsett, Austin Culver, Jamal Egbaria, Austin Williams, Matt Barnes, Raeann Lamere, Austin R Rossi, Stephanie C Waldrep, Caroline Wilder, Elliot Kliossis, Melanie L Styers
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引用次数: 3

Abstract

The yeast vacuole plays key roles in cellular stress responses. Here, we show that deletion of lvs1, the fission yeast homolog of the Chediak-Higashi Syndrome CHS1/LYST gene, increases vacuolar size, similar to deletion of the Rab4 homolog ypt4. Overexpression of lvs1-YFP rescued vacuolar size in ypt4Δ cells, but ypt4-YFP did not rescue lvs1Δ, suggesting that lvs1 may act downstream of ypt4. Vacuoles were capable of hypotonic shock-induced fusion and recovery in both ypt4Δ and lvs1Δ cells, although recovery may be slightly delayed in ypt4Δ. Endocytic and secretory trafficking were not affected, but ypt4Δ and lvs1Δ strains were sensitive to neutral pH and CaCl2, consistent with vacuolar dysfunction. In addition to changes in vacuolar size, deletion of ypt4 also dramatically increased cell size, similar to tor1 mutants. These results implicate ypt4 and lvs1 in maintenance of vacuolar size and suggest that ypt4 may link vacuolar homeostasis to cell cycle progression.

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Ypt4和lvs1调节裂糖菌液泡大小和功能。
酵母液泡在细胞应激反应中起关键作用。在这里,我们发现,与Chediak-Higashi综合征CHS1/LYST基因的裂变酵母同源物lvs1的缺失,增加了液泡的大小,类似于Rab4同源物的缺失。过表达lvs1- yfp可以挽救ypt4Δ细胞的空泡大小,但ypt4- yfp不能挽救lvs1Δ,这表明lvs1可能作用于ypt4的下游。液泡能够在低渗休克诱导下在ypt4Δ和lvs1Δ细胞中融合和恢复,尽管在ypt4Δ中恢复可能稍微延迟。内吞和分泌运输不受影响,但ypt4Δ和lvs1Δ菌株对中性pH和CaCl2敏感,与空泡功能障碍一致。除了液泡大小的变化外,ypt4的缺失也显著增加了细胞大小,类似于tor1突变体。这些结果提示ypt4和lvs1参与液泡大小的维持,并提示ypt4可能将液泡稳态与细胞周期进程联系起来。
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