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钙调蛋白拮抗剂对粗糙脉孢菌昼夜分生孢子形成节律的相移作用

Phase shifting of the circadian conidiation rhythm in Neurospora crassa by calmodulin antagonists.

作者信息

Nakashima H

机构信息

National Institute for Basic Biology, Myodaijicho, Okazaki, Japan.

出版信息

J Biol Rhythms. 1986 Summer;1(2):163-9. doi: 10.1177/074873048600100207.

Abstract

The effects of chemicals capable of antagonizing the functions of calmodulin, such as trifluoperazine, chlorpromazine, imipramine, alprenolol, W7, and W13, on the circadian conidiation rhythm of Neurospora crassa were examined. Trifluoperazine, at a 30-microM concentration, was most effective in shifting the phase of the conidiation rhythm and caused a maximum phase delay at circadian time (CT) 6 and maximum phase advance at CT 9. Chlorpromazine was less effective than trifluoperazine, and a 300-microM concentration of chlorpromazine was required for a similar phase shift. Imipramine, at a 1-mM concentration, caused only a small phase shift, while alprenolol had little effect on biological clock function. W7 and W13 caused phase delays longer than 10 hr at CT 6 and caused a phase advance of about 5 hr at CT 10 when present at a 200-microM concentration. However, W5 and W12, the dechlorinated homologues of W7 and W13, had no effects on clock function at the same concentration. Calmodulin was assayed by measurements of stimulation of cyclic nucleotide diphosphodiesterase activity. Calmodulin content remained constant in trifluoperazine-sensitive and trifluoperazine-insensitive phases for two cycles following the light-dark transition.

摘要

研究了能够拮抗钙调蛋白功能的化学物质,如三氟拉嗪、氯丙嗪、丙咪嗪、阿普洛尔、W7和W13,对粗糙脉孢菌昼夜分生孢子形成节律的影响。三氟拉嗪在30微摩尔浓度时,对分生孢子形成节律的相位改变最有效,在昼夜时间(CT)6时引起最大相位延迟,在CT 9时引起最大相位提前。氯丙嗪的效果不如三氟拉嗪,需要300微摩尔浓度的氯丙嗪才能产生类似的相位变化。丙咪嗪在1毫摩尔浓度时仅引起较小的相位变化,而阿普洛尔对生物钟功能影响很小。W7和W13在200微摩尔浓度时,在CT 6时引起超过10小时的相位延迟,在CT 10时引起约5小时的相位提前。然而,W7和W13的脱氯同系物W5和W12在相同浓度下对生物钟功能没有影响。通过测量环核苷酸二磷酸酯酶活性的刺激来测定钙调蛋白。在明暗转换后的两个周期中,钙调蛋白含量在对三氟拉嗪敏感和不敏感的阶段保持恒定。

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