Jakubowski H, Goldman E
Department of Microbiology and Molecular Genetics, UMDNJ-New Jersey Medical School, Newark 07103.
Mol Cell Biol. 1988 Dec;8(12):5166-78. doi: 10.1128/mcb.8.12.5166-5178.1988.
Diploid Saccharomyces cerevisiae cells heterozygous for the mating type locus (MATa/MAT alpha) undergo meiosis and sporulation when starved for nitrogen in the presence of a poor carbon source such as potassium acetate. Diploid yeast adenine auxotrophs sporulated well at high cell density (10(7) cells per ml) under these conditions but failed to differentiate at low cell density (10(5) cells per ml). The conditional sporulation-deficient phenotype of adenine auxotrophs could be complemented by wild-type yeast cells, by medium from cultures that sporulate at high cell density, or by exogenously added adenine (or hypoxanthine with some mutants). Adenine and hypoxanthine in addition to guanine, adenosine, and numerous nucleotides were secreted into the medium, each in its unique temporal pattern, by sporulating auxotrophic and prototrophic yeast strains. The major source of these compounds was degradation of RNA. The data indicated that differentiating yeast cells cooperate during sporulation in maintaining sufficiently high concentrations of extracellular purines which are absolutely required for sporulation of adenine auxotrophs. Yeast prototrophs, which also sporulated less efficiently at low cell density (10(3) cells per ml), reutilized secreted purines in preference to de novo-made purine nucleotides whose synthesis was in fact inhibited during sporulation at high cell density. Adenine enhanced sporulation of yeast prototrophs at low cell density. The behavior of adenine auxotrophs bearing additional mutations in purine salvage pathway genes (ade apt1, ade aah1 apt1, ade hpt1) supports a model in which secretion of degradation products, uptake, and reutilization of these products is a signal between cells synchronizing the sporulation process.
在交配型位点(MATa/MATα)杂合的二倍体酿酒酵母细胞,在存在如醋酸钾等劣质碳源且缺乏氮源时会进行减数分裂和孢子形成。在这些条件下,二倍体酵母腺嘌呤营养缺陷型在高细胞密度(每毫升10⁷个细胞)时能良好地形成孢子,但在低细胞密度(每毫升10⁵个细胞)时无法分化。腺嘌呤营养缺陷型的条件性孢子形成缺陷表型可被野生型酵母细胞、高细胞密度下形成孢子的培养物的培养基或外源添加的腺嘌呤(或某些突变体的次黄嘌呤)所互补。正在形成孢子的营养缺陷型和原养型酵母菌株会将腺嘌呤、次黄嘌呤以及鸟嘌呤、腺苷和许多核苷酸分泌到培养基中,每种物质都有其独特的时间模式。这些化合物的主要来源是RNA的降解。数据表明,正在分化的酵母细胞在孢子形成过程中相互协作,以维持足够高浓度的细胞外嘌呤,而这是腺嘌呤营养缺陷型孢子形成所绝对必需的。原养型酵母在低细胞密度(每毫升10³个细胞)时孢子形成效率也较低,它们优先重新利用分泌的嘌呤,而不是在高细胞密度下孢子形成期间实际上被抑制合成的从头合成的嘌呤核苷酸。腺嘌呤可增强低细胞密度下原养型酵母的孢子形成。携带嘌呤补救途径基因额外突变(ade apt1、ade aah1 apt1、ade hpt1)的腺嘌呤营养缺陷型的行为支持这样一种模型,即降解产物的分泌、摄取和这些产物的重新利用是细胞间同步孢子形成过程的信号。