Suppr超能文献

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.

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。

相似文献

1
Genetics of the deflagellation pathway in Chlamydomonas.衣藻中去鞭毛途径的遗传学
Genetics. 1998 Jun;149(2):927-36. doi: 10.1093/genetics/149.2.927.

引用本文的文献

1
Assembly of FAP93 at the proximal axoneme in Chlamydomonas cilia.在衣藻纤毛的近端轴丝上组装 FAP93。
Cytoskeleton (Hoboken). 2024 Nov;81(11):539-555. doi: 10.1002/cm.21818. Epub 2024 Jan 15.
2
Shedding of ciliary vesicles at a glance.一眼看过去纤毛小泡脱落。
J Cell Sci. 2022 Oct 1;135(19). doi: 10.1242/jcs.246553. Epub 2022 Oct 12.
4
MKS-NPHP module proteins control ciliary shedding at the transition zone.MKS-NPHP 模块蛋白控制纤毛在过渡区的脱落。
PLoS Biol. 2020 Mar 12;18(3):e3000640. doi: 10.1371/journal.pbio.3000640. eCollection 2020 Mar.
8
The centrosome and its duplication cycle.中心体及其复制周期。
Cold Spring Harb Perspect Biol. 2015 Feb 2;7(2):a015800. doi: 10.1101/cshperspect.a015800.

本文引用的文献

4
Nutritional studies with Chlamydomonas reinhardi.莱茵衣藻的营养研究。
Ann N Y Acad Sci. 1953 Oct 14;56(5):831-8. doi: 10.1111/j.1749-6632.1953.tb30261.x.
6
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.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验