Held Lewis Irving, Duarte Christine Marie, Derakhshanian Kourosh
Developmental Biology Center, University of California, 92717, Irvine, California, USA.
Rouxs Arch Dev Biol. 1986 Apr;195(3):145-157. doi: 10.1007/BF02439432.
The legs of flies from 16 different mutant strains ofDrosophila melanogaster were examined for abnormal cuticular polarities and extra joints. The strains were chosen for study because they manifest abnormal cuticular polarities in some parts of the body (10 strains) or because they have missing or defective tarsal joints (6 strains). All but three of the stocks were found to exhibit misorientations of either the bristles, hairs, or "bract-socket vectors" on the legs. The latter term denotes an imaginary vector pointing from a hairlike structure called a "bract" to the bristle socket with which it is associated. On the legs of wild-type flies nearly all such vectors point distally, as do the bristles and hairs. In the mutant flies, the most common vector misorientation is a 180° reversal. When the bract-socket vectors of adjacent bristle sites in the same bristle row point toward one another, the distance between the sites is frequently abnormally large, whereas when the vectors point in opposite directions, the interval is frequently abnormally small. This correlation is interpreted to mean that bristle cells actively repel one another via cytoplasmic extensions that are longer in the direction of the bract-socket vector than in the opposite direction. Repulsive forces of this kind may be responsible for "fine-tuning" the regularity of bristle spacing in wild-type flies.Extra tarsal joints were found in eight of the 16 strains. A ninth strain completely lacking tarsal joints appears in some cases to have an extra tibia-basitarsus joint in its tibia. Whereas the tarsi of wild-type flies contain four joints, the tarsi ofspiny legs mutant flies contain as many as eight joints. In this extreme extra-joint phenotype, four of the joints correspond to the normal wild-type joints, and there is an extra joint in every tarsal segment except the distal-most (fifth) segment. Nearly all such ectopic extra joints have inverted polarity. In other strains the extra tarsal joints are located mainly at the wild-type joint sites, and joints of this sort have wild-type polarity. The alternation of normal and inverted (extra) joints inspiny legs resembles the alternation of normal and inverted (extra) body segment boundaries in the embryonic-lethal mutantpatch, suggesting that tarsal and body segmentation may share a common patterning mechanism.
对来自16种不同突变品系的黑腹果蝇的腿部进行了检查,以观察其表皮极性异常和额外关节情况。选择这些品系进行研究是因为它们在身体某些部位表现出表皮极性异常(10个品系),或者因为它们有跗关节缺失或缺陷(6个品系)。除了三个品系外,其余所有品系的腿部刚毛、毛发或“苞片 - 刚毛囊载体”均出现了方向错误。后一个术语表示一个假想的向量,从一种称为“苞片”的毛发状结构指向与其相关的刚毛囊。在野生型果蝇的腿部,几乎所有这些向量都指向远端,刚毛和毛发也是如此。在突变果蝇中,最常见的向量方向错误是180°反转。当同一刚毛排中相邻刚毛位点的苞片 - 刚毛囊向量彼此指向对方时,位点之间的距离通常异常大,而当向量指向相反方向时,间隔通常异常小。这种相关性被解释为意味着刚毛细胞通过细胞质延伸相互主动排斥,这些延伸在苞片 - 刚毛囊向量方向上比在相反方向上更长。这种排斥力可能负责“微调”野生型果蝇中刚毛间距的规律性。在16个品系中的8个品系中发现了额外的跗关节。第九个品系完全没有跗关节,在某些情况下其胫骨似乎有一个额外的胫 - 基跗关节。野生型果蝇的跗节有四个关节,而多刺腿突变果蝇的跗节多达八个关节。在这种极端的额外关节表型中,四个关节与正常野生型关节相对应,除了最远端(第五)节段外,每个跗节段都有一个额外的关节。几乎所有这些异位额外关节都具有反向极性。在其他品系中,额外的跗关节主要位于野生型关节位点,并且这种关节具有野生型极性。多刺腿中正常和反向(额外)关节的交替类似于胚胎致死突变体斑块中正常和反向(额外)身体节段边界的交替,这表明跗节和身体节段划分可能共享一种共同的模式形成机制。