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Studies on the flagella of algae. V. Serology of paralyzed mutants of Chlamydomonas.藻类鞭毛研究。五、衣藻麻痹突变体的血清学
Can J Microbiol. 1954 Aug;1(1):65-7. doi: 10.1139/m55-009.
2
Activation of adenylyl cyclase in Chlamydomonas reinhardtii by adhesion and by heat.莱茵衣藻中腺苷酸环化酶通过黏附作用和热作用被激活。
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3
The role of calcium in the Chlamydomonas reinhardtii mating reaction.钙在莱茵衣藻交配反应中的作用。
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4
Mechanisms of flagellar excision. I. The role of intracellular acidification.鞭毛切除的机制。I. 细胞内酸化的作用。
Exp Cell Res. 1993 Sep;208(1):148-53. doi: 10.1006/excr.1993.1232.
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Cloning of flagellar genes in Chlamydomonas reinhardtii by DNA insertional mutagenesis.通过DNA插入诱变克隆莱茵衣藻的鞭毛基因。
Genetics. 1993 Oct;135(2):375-84. doi: 10.1093/genetics/135.2.375.
6
Deflagellation of Chlamydomonas reinhardtii follows a rapid transitory accumulation of inositol 1,4,5-trisphosphate and requires Ca2+ entry.莱茵衣藻的鞭毛去除伴随着肌醇1,4,5-三磷酸的快速短暂积累,并且需要钙离子进入。
J Cell Biol. 1993 Nov;123(4):869-75. doi: 10.1083/jcb.123.4.869.
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Identification of katanin, an ATPase that severs and disassembles stable microtubules.鉴定katanin,一种能切断并拆解稳定微管的ATP酶。
Cell. 1993 Nov 5;75(3):419-29. doi: 10.1016/0092-8674(93)90377-3.
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Centrin plays an essential role in microtubule severing during flagellar excision in Chlamydomonas reinhardtii.中心蛋白在莱茵衣藻鞭毛切除过程中的微管切断中起着至关重要的作用。
J Cell Biol. 1994 Mar;124(5):795-805. doi: 10.1083/jcb.124.5.795.
9
Tipping of flagellar agglutinins by gametes of Chlamydomonas reinhardtii.莱茵衣藻配子对鞭毛凝集素的翻转
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New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures.新型对镁离子和质子具有高选择性的钙指示剂和缓冲剂:原型结构的设计、合成及性质
Biochemistry. 1980 May 27;19(11):2396-404. doi: 10.1021/bi00552a018.

两条不同的、钙介导的信号转导途径可触发莱茵衣藻的鞭毛脱除。

Two distinct, calcium-mediated, signal transduction pathways can trigger deflagellation in Chlamydomonas reinhardtii.

作者信息

Quarmby L M, Hartzell H C

机构信息

Department of Physiology, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

J Cell Biol. 1994 Mar;124(5):807-15. doi: 10.1083/jcb.124.5.807.

DOI:10.1083/jcb.124.5.807
PMID:8120101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2119959/
Abstract

The molecular machinery of deflagellation can be activated in detergent permeabilized Chlamydomonas reinhardtii by the addition of Ca2+ (Sanders, M. A., and J. L. Salisbury, 1989. J. Cell Biol. 108:1751-1760). This suggests that stimuli which induce deflagellation in living cells cause an increase in the intracellular concentration of Ca2+, but this has never been demonstrated. In this paper we report that the wasp venom peptide, mastoparan, and the permeant organic acid, benzoate, activate two different signalling pathways to trigger deflagellation. We have characterized each pathway with respect to: (a) the requirement for extracellular Ca2+; (b) sensitivity to Ca2+ channel blockers; and (c) 45Ca influx. We also report that a new mutant strain of C. reinhardtii, adf-1, is specifically defective in the acid-activated signalling pathway. Both signalling pathways appear normal in another mutant, fa-1, that is defective in the machinery of deflagellation (Lewin, R. and C. Burrascano. 1983. Experientia. 39:1397-1398; Sanders, M. A., and J. L. Salisbury. 1989. J. Cell Biol. 108:1751-1760). We conclude that mastoparan induces the release of an intracellular pool of Ca2+ whereas acid induces an influx of extracellular Ca2+ to activate the machinery of deflagellation.

摘要

通过添加Ca2+,去鞭毛的分子机制可以在经去污剂通透处理的莱茵衣藻中被激活(桑德斯,M. A.,和J. L. 索尔兹伯里,1989年。《细胞生物学杂志》108:1751 - 1760)。这表明在活细胞中诱导去鞭毛的刺激会导致细胞内Ca2+浓度升高,但这从未得到证实。在本文中,我们报告黄蜂毒液肽、马斯托帕兰和渗透性有机酸苯甲酸酯激活两种不同的信号通路来触发去鞭毛。我们已经从以下几个方面对每条通路进行了表征:(a)对细胞外Ca2+的需求;(b)对Ca2+通道阻滞剂的敏感性;以及(c)45Ca内流。我们还报告了莱茵衣藻的一个新突变株adf - 1,它在酸激活的信号通路中存在特异性缺陷。在另一个去鞭毛机制存在缺陷的突变体fa - 1中,这两种信号通路看起来正常(莱文,R. 和C. 布拉斯卡诺。1983年。《实验》39:1397 - 1398;桑德斯,M. A.,和J. L. 索尔兹伯里。1989年。《细胞生物学杂志》108:1751 - 1760)。我们得出结论,马斯托帕兰诱导细胞内Ca2+池的释放,而酸诱导细胞外Ca2+内流以激活去鞭毛机制。