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Propranolol atenolol and trifluoperazine reduce the spontaneous occurrence of meiotic diploid products in Saccharomyces cerevisiae.

机译:普萘洛尔阿替洛尔和三氟哌嗪可减少酿酒酵母中减数分裂二倍体产物的自发发生。

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摘要

The effect of atenolol, propranolol, trifluoperazine, and caffeine on the occurrence of meiotic diploid and disomic products in Saccharomyces cerevisiae was investigated. We demonstrated that atenolol, propranolol, and trifluoperazine reduce the occurrence of meiotic diploid products and that propranolol also slightly decreases the spontaneous frequency of disomics. On the other hand, caffeine appears to be a powerful inducer of diploid meiotic products, but also shows a lesser effect on disomic induction. Since spontaneous or caffeine-induced diploids arise from a failure of the second meiotic division, it appears that the target of these drugs is at the beginning of the second meiotic division. The only common effect of trifluoperazine and propranolol, mainly investigated in mammals, was an inhibition of calmodulin activity via direct interaction. We tend, therefore, to believe that calmodulin activity must be a crucial point for the second meiotic division to begin. The increased induction of diploids, due to caffeine, may be interpreted as a consequence of an increased cyclic AMP level.
机译:研究了阿替洛尔,普萘洛尔,三氟拉嗪和咖啡因对酿酒酵母中减数分裂二倍体和二体产物产生的影响。我们证明了阿替洛尔,普萘洛尔和三氟拉嗪减少了减数分裂二倍体产物的发生,而普萘洛尔也略微降低了组学的自发频率。另一方面,咖啡因似乎是二倍体减数分裂产物的有力诱导剂,但对二体组诱导作用较小。由于自发性或咖啡因诱导的二倍体是第二次减数分裂分裂的失败,因此这些药物的靶点似乎在第二个减数分裂分裂的开始。主要在哺乳动物中研究的氟氟哌嗪和普萘洛尔的唯一共同作用是通过直接相互作用抑制钙调蛋白活性。因此,我们倾向于认为钙调蛋白活性必须是第二个减数分裂分裂开始的关键点。由于咖啡因,导致二倍体的诱导增加可能是循环AMP水平升高的结果。

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