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酿酒酵母cdc25突变体中腺苷酸环化酶的激活。

Activation of adenylate cyclase in cdc25 mutants of Saccharomyces cerevisiae.

作者信息

Pardo L A, Lazo P S, Ramos S

机构信息

Departamento de Biología Funcional, Universidad de Oviedo, Spain.

出版信息

FEBS Lett. 1993 Mar 22;319(3):237-43. doi: 10.1016/0014-5793(93)80554-8.

Abstract

The activation of adenylate cyclase by guanine nucleotides and 6-deoxyglucose was studied in membrane preparations from S. cerevisiae mutants lacking the CDC25 gene product. Adenylate cyclase from cdc25 ts membranes was activated by GTP and GppNHp in membranes from cells collected after glucose was exhausted from the medium. The activation was also observed in membranes from repressed cells at 2.5 mM Mg2+. It is also shown that 6-deoxyglucose can activate adenylate cyclase in the absence of CDC25 gene product. The relative amount of membrane-bound adenylate cyclase was drastically reduced in cdc25 ts membranes when subjected to the restrictive temperature, while no significant change was observed in the wild type. These data suggest that Cdc25 might not be required in certain conditions for the guanine nucleotide exchange reaction in Ras and that it might be implicated in anchoring the Ras/adenylate cyclase system to the plasma membrane.

摘要

在缺乏CDC25基因产物的酿酒酵母突变体的膜制剂中,研究了鸟嘌呤核苷酸和6-脱氧葡萄糖对腺苷酸环化酶的激活作用。在培养基中的葡萄糖耗尽后收集的细胞的膜中,来自cdc25温度敏感型(ts)膜的腺苷酸环化酶被GTP和GppNHp激活。在2.5 mM Mg2+存在下,在受抑制细胞的膜中也观察到了这种激活作用。还表明,在没有CDC25基因产物的情况下,6-脱氧葡萄糖可以激活腺苷酸环化酶。当处于限制温度时,cdc25 ts膜中膜结合腺苷酸环化酶的相对量急剧减少,而野生型中未观察到显著变化。这些数据表明,在某些条件下,Ras中的鸟嘌呤核苷酸交换反应可能不需要Cdc25,并且它可能与将Ras/腺苷酸环化酶系统锚定到质膜有关。

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