首页> 外文期刊>Eukaryotic cell >Polarized Morphogenesis Regulator Spa2 Is Required for the Function of Putative Stretch-Activated Ca2+-Permeable Channel Component Mid1 in Saccharomyces cerevisiae
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Polarized Morphogenesis Regulator Spa2 Is Required for the Function of Putative Stretch-Activated Ca2+-Permeable Channel Component Mid1 in Saccharomyces cerevisiae

机译:极化的形态发生调节剂Spa2是酿酒酵母中推定激活的Ca2 +渗透通道成分Mid1的功能所必需的

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Mid1 is a putative stretch-activated Ca2+ channel component and is required for the maintenance of viability in the mating process. In response to mating pheromone, the mid1 mutant normally forms a pointed mating projection but eventually dies. This phenotype is called the mid phenotype. To identify a protein regulating Mid1 or regulated by Mid1, we isolated a multicopy suppressor that rescues the mid1-1 mutant from mating pheromone-induced death and found that it encodes a truncated Spa2 protein lacking an amino-terminal region responsible for interaction with components of the mitogen-activated protein kinase cascades. One of these SPA2 alleles was SPA2ΔN, whose product lacked the region from Ser5 to Leu230. SPA2ΔN on a multicopy plasmid (YEpSPA2ΔN) complemented the mid phenotype but not another phenotype, low Ca2+ accumulation, of the mid1-1 mutant. Neither SPA2ΔN on a low-copy plasmid nor wild-type SPA2 on a multicopy plasmid had suppressive activity. The SPA2 gene is involved in the formation of a pointed mating projection, and cells of the spa2Δ mutant lacking Spa2 are viable and develop a peanut shell-like structure when exposed to mating pheromone. Like the spa2Δ mutant, the mid1-1 spa2Δ double mutant and the mid1-1/YEpSPA2ΔN strain developed the peanut shell-like structure. The mid1-1 spa2Δ double mutant did not have the mid phenotype, indicating that SPA2 is epistatic to MID1. Overexpression of Spa2ΔN abolished the localization of Spa2-green fluorescent protein to the tip of the mating projection. These results suggest that the Spa2ΔN protein interferes with the localization of the normal Spa2 protein and thereby prevents cells from entering the mating process. Therefore, we suggest that Mid1 function is influenced by Spa2 function through polarized morphogenesis.
机译:Mid1是推定激活的Ca 2 + 通道成分,是维持交配过程中生存力所必需的。作为对交配信息素的响应, mid1 突变体通常形成一个尖的交配投影,但最终死亡。该表型称为中间表型。为了鉴定调节Mid1或受Mid1调节的蛋白,我们分离了一种多拷贝抑制子,该蛋白从交配信息素诱导的死亡中拯救 mid1 - 1 突变体,并发现其编码为截短的Spa2蛋白缺少一个负责与丝裂原激活的蛋白激酶级联反应的成分相互作用的氨基末端区域。这些 SPA2 等位基因之一是 SPA2 Δ N ,其产物缺少从Ser 5 到Leu 230 。多拷贝质粒(YEpSPA2ΔN)上的 SPA2 Δ N 补充了的中间表型,但没有另一个表型,即低Ca 2 + 积累> mid1 - 1 突变体。低拷贝质粒上的 SPA2 Δ N 和多拷贝质粒上的野生型 SPA2 都没有抑制活性。 SPA2 基因参与了尖的交配突起的形成,而缺少Spa2的 spa2 Δ突变体的细胞是有活力的,并且暴露于花生壳样结构中交配信息素。与 spa2 Δ突变体一样, mid1 - 1 spa2 Δ双突变体和 mid1 - 1 / YEpSPA2ΔN菌株形成了花生壳状结构。 mid1 - 1 spa2 Δ双突变体没有中间表型,表明 SPA2 MID1 上位。 Spa2ΔN的过表达消除了Spa2-绿色荧光蛋白在交配突起末端的定位。这些结果表明,Spa2ΔN蛋白干扰正常Spa2蛋白的定位,从而阻止细胞进入交配过程。因此,我们建议Mid1功能受极化形态发生的Spa2功能的影响。

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