Wright R, Keller G, Gould S J, Subramani S, Rine J
University of California, Department of Molecular and Cellular Biology, Berkeley, CA 94720.
New Biol. 1990 Oct;2(10):915-21.
Quantitative increases in HMG-CoA reductase, the rate-limiting enzyme in sterol biosynthesis, induce membrane biogenesis in both yeast and mammalian cells. The subcellular organization of the resulting membrane differs in the two cell types: mammalian cells generate crystalloid endoplasmic reticulum whereas yeast cells assemble karmellae. We examined the consequences of heterologous expression of HMG-CoA reductase to distinguish features of this response that were cell-type specific from those that were isozyme-specific. This analysis demonstrated that membrane proliferation was induced in both mammalian and yeast cells by HMG-CoA reductase from either organism. However, the morphology of the induced membranes was determined by the cell type rather than the particular isozyme. Thus, both yeast and mammalian HMG-CoA reductase contained functional signals for membrane proliferation that were operational in either cell type, but the qualitative response to those signals was cell-type specific.
HMG-CoA还原酶是固醇生物合成中的限速酶,其数量增加会在酵母细胞和哺乳动物细胞中诱导膜生物发生。在这两种细胞类型中,所产生膜的亚细胞组织有所不同:哺乳动物细胞产生晶体状内质网,而酵母细胞组装卡氏小体。我们研究了HMG-CoA还原酶异源表达的后果,以区分这种反应中细胞类型特异性特征和同工酶特异性特征。该分析表明,来自任一生物体的HMG-CoA还原酶均可在哺乳动物细胞和酵母细胞中诱导膜增殖。然而,诱导膜的形态由细胞类型而非特定同工酶决定。因此,酵母和哺乳动物的HMG-CoA还原酶均含有膜增殖的功能性信号,这些信号在任一细胞类型中均可发挥作用,但对这些信号的定性反应具有细胞类型特异性。