Frankel J, Nelsen E M
Department of Biology, University of Iowa, Iowa City 52242.
Development. 1987 Jan;99(1):51-68. doi: 10.1242/dev.99.1.51.
The janus mutations of Tetrahymena thermophila convert the large-scale organization of the dorsal surface of the cell into a mirror-image of the ventral surface, which is characterized by a second, abnormal, oral apparatus and by contractile vacuole pores to the left of the second oral area rather than the usual right. This conversion could be due either to a local change in the response to an unaltered positional system or to a more global reorganization of the system itself. janus homopolar doublets were used to distinguish between these two alternatives. Homopolar doublets can be made by fusing two similarly oriented cells in side-by-side parabiosis. Non-janus homopolar doublets typically possess two sets of normal oral structures with contractile vacuole pores to the right of each of them. In janus doublets, there are up to four sets of oral structures, with the abnormal oral structures located between the two sets of normal oral structures; contractile vacuole pores are situated to the right of the normal oral areas and to the left of the abnormal oral structures. Non-janus homopolar doublets are known to propagate their compound condition for a number of cell divisions, but also to regulate toward the singlet state through a progressive reduction in number of ciliary rows followed by loss of one of the two sets of major cell surface structures. janus homopolar doublets go through a corresponding regulation. As a consequence, the location of the abnormal oral structures relative to the normal ones is more variable in janus doublets than in janus singlets. Sometimes the abnormal oral structures shift to a position close to their normal counterparts and then the intervening CVP sets disappear. There is evidence for occasional fusion of an abnormal oral area with an adjacent normal oral apparatus, a condition that may be transitional to the singlet state. These observations are inconsistent with the idea of a fixed positional system and strongly suggest a global reorganization of the surface pattern in a manner consistent with predictions of an intercalation model that was first proposed to explain the regulation of non-janus doublets to singlets.
嗜热四膜虫的“两面神”突变将细胞背面的大规模组织结构转变为腹面的镜像,其特征是出现第二个异常口器,并且收缩泡孔位于第二个口区的左侧而非通常的右侧。这种转变可能是由于对未改变的位置系统的反应发生局部变化,或者是由于系统本身更全面的重组。使用“两面神”同极双联体来区分这两种可能性。同极双联体可以通过将两个方向相同的细胞并排联体融合而成。非“两面神”同极双联体通常拥有两组正常的口器结构,每组口器结构的右侧都有收缩泡孔。在“两面神”双联体中,有多达四组口器结构,异常口器结构位于两组正常口器结构之间;收缩泡孔位于正常口区的右侧和异常口器结构的左侧。已知非“两面神”同极双联体在多个细胞分裂过程中会延续其复合状态,但也会通过纤毛排数逐渐减少,随后丢失两组主要细胞表面结构之一来向单体状态调节。“两面神”同极双联体也经历相应的调节。因此,与“两面神”单体相比,“两面神”双联体中异常口器结构相对于正常口器结构的位置变化更大。有时异常口器结构会移至靠近其正常对应物的位置,然后中间的收缩泡孔组消失。有证据表明异常口区偶尔会与相邻的正常口器融合,这种情况可能是向单体状态转变的过渡阶段。这些观察结果与固定位置系统的观点不一致,并强烈表明表面模式发生了全面重组,其方式与最初提出用于解释非“两面神”双联体向单体调节的插入模型的预测一致。