Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06519, USA.
Mol Biol Cell. 2010 May 15;21(10):1772-82. doi: 10.1091/mbc.e09-06-0532. Epub 2010 Mar 31.
Inheritance of the endoplasmic reticulum (ER) requires Ptc1p, a type 2C protein phosphatase of Saccharomyces cerevisiae. Genetic analysis indicates that Ptc1p is needed to inactivate the cell wall integrity (CWI) MAP kinase, Slt2p. Here we show that under normal growth conditions, Ptc1p inactivates Slt2p just as ER tubules begin to spread from the bud tip along the cortex. In ptc1Delta cells, the propagation of cortical ER from the bud tip to the periphery of the bud is delayed by hyperactivation of Slt2p. The pool of Slt2p that controls ER inheritance requires the CWI pathway scaffold, Spa2p, for its retention at the bud tip, and a mutation within Slt2p that prevents its association with the bud tip blocks its role in ER inheritance. These results imply that Slt2p inhibits a late step in ER inheritance by phosphorylating a target at the tip of daughter cells. The PI4P5-kinase, Mss4p, is an upstream activator of this pool of Slt2p. Ptc1p-dependant inactivation of Slt2p is also needed for mitochondrial inheritance; however, in this case, the relevant pool of Slt2p is not at the bud tip.
内质网(ER)的遗传需要 Ptc1p,这是一种酿酒酵母的 2C 型蛋白磷酸酶。遗传分析表明,Ptc1p 需要失活细胞壁完整性(CWI)MAP 激酶 Slt2p。在这里,我们发现,在正常生长条件下,当内质网管从芽尖沿着皮层扩散时,Ptc1p 就会使 Slt2p 失活。在 ptc1Δ细胞中,由于 Slt2p 的过度激活,从芽尖到芽的外周的皮层 ER 的传播被延迟。控制 ER 遗传的 Slt2p 池需要 CWI 途径支架 Spa2p 将其保留在芽尖,并且 Slt2p 内的一个突变阻止了其与芽尖的结合,从而阻止了其在 ER 遗传中的作用。这些结果表明,Slt2p 通过磷酸化子细胞尖端的靶标来抑制 ER 遗传的后期步骤。PI4P5-激酶 Mss4p 是该池 Slt2p 的上游激活剂。Ptc1p 依赖性 Slt2p 失活对于线粒体遗传也是必需的;然而,在这种情况下,相关的 Slt2p 池不在芽尖。