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Sex-limited expression of gene Loci controlling flagellar membrane agglutination in the chlamydomonas mating reaction.控制衣滴虫交配反应中鞭毛膜聚集的基因座在性别限制表达。
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Microtubule dynamics: severing microtubules in mitosis.微管动力学:在有丝分裂中切断微管。
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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
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Nutritional studies with Chlamydomonas reinhardi.莱茵衣藻的营养研究。
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A role for katanin-mediated axonemal severing during Chlamydomonas deflagellation.卡塔宁介导的轴丝切断在衣藻去鞭毛过程中的作用。
Mol Biol Cell. 1998 May;9(5):1195-207. doi: 10.1091/mbc.9.5.1195.
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The cell center at 100.细胞中心值为100。
Cell. 1997 Oct 31;91(3):303-9. doi: 10.1016/s0092-8674(00)80414-6.
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Ion selectivity in the Chlamydomonas reinhardtii flagellar regeneration system.莱茵衣藻鞭毛再生系统中的离子选择性
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Most of centrin in animal cells is not centrosome-associated and centrosomal centrin is confined to the distal lumen of centrioles.动物细胞中的大多数中心蛋白并不与中心体相关联,且中心体中心蛋白局限于中心粒的远端管腔。
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Katanin, the microtubule-severing ATPase, is concentrated at centrosomes.katanin,一种可切断微管的ATP酶,集中于中心体。
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10
Centrin is a conserved protein that forms diverse associations with centrioles and MTOCs in Naegleria and other organisms.中心蛋白是一种保守蛋白,在耐格里属变形虫和其他生物体中与中心粒和微管组织中心形成多种关联。
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衣藻中去鞭毛途径的遗传学

Genetics of the deflagellation pathway in Chlamydomonas.

作者信息

Finst R J, Kim P J, Quarmby L M

机构信息

Department of Cell Biology, Cell & Developmental Biology, Emory University School of Medicine, Atlanta, Georgia 30322-3030, USA.

出版信息

Genetics. 1998 Jun;149(2):927-36. doi: 10.1093/genetics/149.2.927.

DOI:10.1093/genetics/149.2.927
PMID:9611203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1460167/
Abstract

Signal-induced deflagellation in Chlamydomonas involves Ca2+-activated breakage of the nine outer-doublet axonemal microtubules at a specific site in the flagellar transition zone. In this study, we isolated 13 new deflagellation mutants that can be divided into two phenotypic classes, the Adf class and the Fa class. Cells with the Adf deflagellation phenotype are defective in acid-stimulated Ca2+ influx, but can be induced to deflagellate by treatment with nonionic detergent and Ca2+. Genetic analyses show that the five new Adf mutations, as well as the previously identified adf1 mutation, are alleles of the ADF1 gene. Mutants in the second phenotypic class, the Fa mutants, fail to deflagellate in response to any known chemical stimulus and are defective in Ca2+-activated microtubule severing. Genetic analysis of these eight new Fa strains demonstrated that they define two complementation groups, and one of these contains the previously identified fa1 mutation. Diploid analysis showed that five alleles map to the FA1 gene, whereas four alleles define a novel gene that we have named FA2. The isolation of multiple mutant alleles of each gene, generated by either ultraviolet irradiation or insertional mutagenesis, indicates that ADF1, FA1, and FA2 may be the only genes that can be identified in a loss-of-function screen. These alleles should provide a better understanding of the regulation of microtubule severing by Ca2+.

摘要

衣藻中信号诱导的鞭毛解聚涉及鞭毛过渡区特定位点处由钙离子激活的九根外双联轴丝微管的断裂。在本研究中,我们分离出了13个新的鞭毛解聚突变体,它们可分为两个表型类别,即Adf类和Fa类。具有Adf鞭毛解聚表型的细胞在酸刺激的钙离子内流方面存在缺陷,但可以通过用非离子去污剂和钙离子处理来诱导其鞭毛解聚。遗传分析表明,这五个新的Adf突变以及先前鉴定出的adf1突变都是ADF1基因的等位基因。第二个表型类别的突变体,即Fa突变体,对任何已知化学刺激均无鞭毛解聚反应,并且在钙离子激活的微管切断方面存在缺陷。对这八个新的Fa菌株的遗传分析表明,它们定义了两个互补群,其中一个包含先前鉴定出的fa1突变。二倍体分析表明,五个等位基因定位于FA1基因,而四个等位基因定义了一个我们命名为FA2的新基因。通过紫外线照射或插入诱变产生的每个基因的多个突变等位基因的分离表明,ADF1、FA1和FA2可能是在功能丧失筛选中能够鉴定出的仅有的基因。这些等位基因应能更好地理解钙离子对微管切断的调控。