Background: Nematode sinusoidal movement has been used as a phenotype in many studies of C. elegans development, behavior and physiology. A thorough understanding of the ways in which genes control these aspects of biology depends, in part, on the accuracy of phenotypic analysis. While worms that move poorly are relatively easy to describe, description of hyperactive movement and movement modulation presents more of a challenge. An enhanced capability to analyze all the complexities of nematode movement will thus help our understanding of how genes control behavior.ududResults: We have developed a user-friendly system to analyze nematode movement in an automated and quantitative manner. In this system nematodes are automatically recognized and a computer-controlled microscope stage ensures that the nematode is kept within the camera field of view while video images from the camera are stored on videotape. In a second step, the images from the videotapes are processed to recognize the worm and to extract its changing position and posture over time. From this information, a variety of movement parameters are calculated. These parameters include the velocity of the worm's centroid, the velocity of the worm along its track, the extent and frequency of body bending, the amplitude and wavelength of the sinusoidal movement, and the propagation of the contraction wave along the body. The length of the worm is also determined and used to normalize the amplitude and wavelength measurements. ududTo demonstrate the utility of this system, we report here a comparison of movement parameters for a small set of mutants affecting the Go/Gq mediated signaling network that controls acetylcholine release at the neuromuscular junction. The system allows comparison of distinct genotypes that affect movement similarly (activation of Gq-alpha versus loss of Go-alpha function), as well as of different mutant alleles at a single locus (null and dominant negative alleles of the goa-1 gene, which encodes Go-alpha). We also demonstrate the use of this system for analyzing the effects of toxic agents. Concentration-response curves for the toxicants arsenite and aldicarb, both of which affect motility, were determined for wild-type and several mutant strains, identifying P-glycoprotein mutants as not significantly more sensitive to either compound, while cat-4 mutants are more sensitive to arsenite but not aldicarb. ududConclusions: Automated analysis of nematode movement facilitates a broad spectrum of experiments. Detailed genetic analysis of multiple alleles and of distinct genes in a regulatory network is now possible. These studies will facilitate quantitative modeling of C. elegans movement, as well as a comparison of gene function. Concentration-response curves will allow rigorous analysis of toxic agents as well as of pharmacological agents. This type of system thus represents a powerful analytical tool that can be readily coupled with the molecular genetics of nematodes.
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机译:背景:线虫正弦运动已在秀丽隐杆线虫的发育,行为和生理学的许多研究中用作表型。对基因控制生物学这些方面的方式的透彻了解部分取决于表型分析的准确性。尽管蠕虫蠕虫运动相对较容易描述,但对活动过度和运动调制的描述却面临着更大的挑战。因此,增强的分析线虫运动所有复杂性的能力将有助于我们了解基因如何控制行为。 ud ud结果:我们已经开发了一种用户友好的系统,可以自动,定量地分析线虫运动。在该系统中,可以自动识别线虫,并且由计算机控制的显微镜载物台可确保将线虫保持在摄像机视场内,同时将来自摄像机的视频图像存储在录像带上。在第二步中,处理来自录像带的图像以识别蠕虫并提取其随时间变化的位置和姿势。根据此信息,可以计算出各种运动参数。这些参数包括蠕虫质心的速度,蠕虫沿其轨迹的速度,身体弯曲的程度和频率,正弦运动的幅度和波长以及收缩波沿身体的传播。还确定了蠕虫的长度,并将其用于归一化幅度和波长测量。 ud ud为了演示此系统的实用性,我们在这里报告了影响Go / Gq介导的控制神经肌肉接头处乙酰胆碱释放的一小部分突变体的运动参数比较。该系统可以比较影响运动的不同基因型(Gq-alpha的激活与Go-alpha功能的丧失),以及单个位点的不同突变等位基因(goa-1基因的无效和显性负等位基因,编码Go-alpha)。我们还演示了使用该系统分析有毒物质的效果。确定了野生型和几种突变菌株的毒物亚砷酸盐和涕灭威的浓度-响应曲线,这两者均影响运动,从而确定P-糖蛋白突变株对这两种化合物的敏感性均不明显,而cat-4突变株的敏感性更高不含亚砷威。结论:线虫运动的自动化分析促进了广泛的实验。现在可以对调控网络中的多个等位基因和不同基因进行详细的遗传分析。这些研究将有助于秀丽隐杆线虫运动的定量建模,以及基因功能的比较。浓度-响应曲线将允许对有毒物质以及药理物质进行严格的分析。因此,这种类型的系统代表了一种功能强大的分析工具,可以轻松地与线虫的分子遗传学结合。
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