Ackermann U, Geering K
Institut de Pharmacologie et de Toxicologie de l'Université, Lausanne, Switzerland.
J Biol Chem. 1992 Jun 25;267(18):12911-5.
Oligomerization of newly synthesized alpha- and beta-subunits is a prerequisite for the structural and functional maturation of Na,K-ATPase. In this study, we have tested the competence of presynthesized alpha- and beta-subunits to assemble into functional enzyme complexes. Antisense oligonucleotides complementary to alpha-mRNA were used to inhibit alpha-subunit synthesis in Xenopus oocytes leaving a presynthesized trypsin-sensitive alpha-subunit pool. beta-Subunits expressed in these oocytes from injected cRNA assembled with the preexisting alpha-subunits, rendered them trypsin-resistant, and permitted the expression of more ouabain binding sites at the plasma membrane. Similarly, presynthesized beta 1- or beta 3-subunits produced in Xenopus oocytes by injection of beta-cRNA and later of specific antisense oligonucleotides were stabilized and transported out of the endoplasmic reticulum when alpha-cRNA was injected into oocytes. These data indicate that alpha- and beta-subunits can insert into endoplasmic reticulum membranes independent of each other in an assembly-competent form and retain their ability for oligomerization after synthesis.
新合成的α亚基和β亚基的寡聚化是钠钾ATP酶结构和功能成熟的先决条件。在本研究中,我们测试了预先合成的α亚基和β亚基组装成功能性酶复合物的能力。与α-mRNA互补的反义寡核苷酸用于抑制非洲爪蟾卵母细胞中的α亚基合成,留下预先合成的对胰蛋白酶敏感的α亚基池。从注射的cRNA在这些卵母细胞中表达的β亚基与预先存在的α亚基组装在一起,使其对胰蛋白酶具有抗性,并允许在质膜上表达更多的哇巴因结合位点。同样,当将α-cRNA注射到卵母细胞中时,通过注射β-cRNA以及随后注射特定反义寡核苷酸在非洲爪蟾卵母细胞中产生的预先合成的β1或β3亚基被稳定化并从内质网中转运出来。这些数据表明,α亚基和β亚基可以以组装能力的形式彼此独立地插入内质网膜,并在合成后保留其寡聚化能力。