Rüffer U, Nultsch W
Fachbereich Biologie der Philipps-Universität Marburg, Germany.
Cell Motil Cytoskeleton. 1998;41(4):297-307. doi: 10.1002/(SICI)1097-0169(1998)41:4<297::AID-CM3>3.0.CO;2-Y.
The two flagella of Chlamydomonas are known to beat synchronously: During breaststroke beating they are generally coordinated in a bilateral way while in shock responses during undulatory beating coordination is mostly parallel [Rüffer and Nultsch, 1995: Botanica Acta 108:169-276]. Analysis of a great number of shock responses revealed that in undulatory beats also periods of bilateral coordination are found and that the coordination type may change several times during a shock response, without concomitant changes of the beat envelope and the beat period. In normal wt cells no coordination changes are found during breaststroke beating, but only short temporary asynchronies: During 2 or 3 normal beats of the cis flagellum, the trans flagellum performs 3 or 4 flat beats with a reduced beat envelope and a smaller beat period, resulting in one additional trans beat. Long periods with flat beats of the same shape and beat period are found in both flagella of the non-phototactic mutant ptx1 and in defective wt 622E cells. During these periods, the coordination is parallel, the two flagella beat alternately. A correlation between normal asynchronous trans beats and the parallel-coordinated beats in the presumably cis defective cells and also the undulatory beats is discussed. In the cis defective cells, a perpetual spontaneous change between parallel beats with small beat periods (higher beat frequency) and bilateral beats with greater beat periods (lower beat frequency) are observed and render questionable the existence of two different intrinsic beat frequencies of the two flagella cis and trans. Asynchronies occur spontaneously but may also be induced by light changes, either step-up or step-down, but not by both stimuli in turn as breaststroke flagellar photoresponses (BFPRs). Asynchronies are not involved in phototaxis. They are independent of the BFPRs, which are supposed to be the basis of phototaxis. Both types of coordination must be assumed to be regulated internally, involving calcium-sensitive basal-body associated fibrous structures.
在蛙泳式摆动期间,它们通常以双侧方式协调,而在波动式摆动的应激反应中,协调大多是平行的[吕弗尔和努尔奇,1995年:《植物学报》108卷:169 - 276页]。对大量应激反应的分析表明,在波动式摆动中也会出现双侧协调期,并且协调类型在应激反应期间可能会多次改变,而搏动包络和搏动周期并无相应变化。在正常野生型细胞的蛙泳式摆动期间未发现协调变化,仅存在短暂的临时不同步情况:在顺式鞭毛正常摆动2或3次期间,反式鞭毛会进行3或4次扁平摆动,其搏动包络减小且搏动周期变小,导致额外一次反式摆动。在非趋光性突变体ptx1和有缺陷的野生型622E细胞的两条鞭毛中都发现了具有相同形状和搏动周期的扁平摆动的长时间周期。在这些周期中,协调是平行的,两条鞭毛交替摆动。文中讨论了正常的异步反式摆动与推测的顺式有缺陷细胞中的平行协调摆动以及波动式摆动之间的相关性。在顺式有缺陷的细胞中,观察到在具有小搏动周期(较高搏动频率)的平行摆动和具有较大搏动周期(较低搏动频率)的双侧摆动之间存在持续的自发变化,这使得两条鞭毛顺式和反式存在两种不同固有搏动频率的说法受到质疑。不同步情况会自发出现,但也可能由光照变化诱导,无论是光照增强还是减弱,但不像蛙泳式鞭毛光反应(BFPRs)那样由两种刺激依次诱导。不同步情况不参与趋光性。它们独立于被认为是趋光性基础的BFPRs。必须假定这两种协调类型都是内部调节的,涉及钙敏感的基体相关纤维结构。