-
[
1987]
Nematode sperm are crawling cells that exhibit a type of locomotion characteristic of an entire class of protozoa as well as numerous embryonic, differentiated, and transformed metazoan cells. Despite considerable variation in morphology and speed of locomotion expressed by these various types of crawling, or amoeboid, cells, there is general agreement that in all cases locomotion is propelled by cytoplasmic contraction involving myosin-induced sliding of actin filaments and regulated, in ways that are not fully understood, by a spectrum of actin-binding proteins. We began to study the motility of sperm of Caenorhabditis elegans hoping to exploit the mutability of this cell in order to analyze the molecular basis of amoeboid movement genetically. Much to our surprise, we discovered that sperm motility is not driven by an actin-based mechanism. Subsequent work, however, has shown that nematode sperm do share many fundamental properties with other amoeboid cells. As a consequence, sperm continue to serve as a profitable model for understanding how cells crawl and, at the same time, have allowed us to examine a new type of cellular motor.
-
Normal development and homeostasis result from a tenuous balance between cell proliferation and cell death. Disruption of this balance, in favor of cell death in particular, could easily lead to pathological states in postmitotic organs such as the adult brain. For example, many neurodegenerative disorders are characterized by the premature death of specific subsets of neurons, which gives rise to their full clinical spectra. Although a complete understanding of the selective cell degeneration in these conditions is still lacking, recent observations suggest that it may occur through apoptosis, a gene-directed type of cell death. In many cases, cell death by apoptosis requires an active role by the dying cells, because apoptosis is most often significantly blocked or delayed by inhibitors of RNA or protein synthesis. This genetic regulation of apoptosis offers a potential for therapeutic intervention and further assessment of apoptotic mechanisms in manifestations of neuropathology is warranted. However, employing conventional molecular and biochemical approaches, attempts to determine the genetic machinery responsible for specifying which cells live and which cells die have not always been successful in vertebrate systems. One organism in which programmed cell death (PCD), a physiological counterpart of apoptosis, has been extensively examined is the nematode Caenorhabditis elegans....
-
[
1983]
The advantages of the free-living nematode Caenrohabditis elegans as a model for pharmacologic, toxicant and anthelmintic testing have become apparent to many companies, and the application of this organism as a primary screen for test compounds or toxic agents has expanded rapidly. It is appropriate to briefly summarize some of this nematode's qualities, to invoke an appreciation of this elegant system. As true of many invertebrate test organisms, C. elegans is small (about 1 mm X 40 u at maturity) and has a short life cycle: reproduction starts on day 3-4, ceases by day 14 and by day 25 it dies. Thus, for aging studies, all the symptoms of senescence are compressed into a short time period. In addition, this nematode has a small, fixed number of cells (about 830 at maturity) and differentiated organ systems: nervous, excretory, muscular, digestive and reproductive. The preceding characteristics are not unique in invertebrate model systems and their enumeration fails to explain the increasing popularity of C. elegans as a test organism. To understand this phenomenon several additional facts must be emphasized. First, the selection of C. elegans for detailed studies on the genetic control and regulation of behavior and developmental processes has fostered a wealth of knowledge on its neuroanatomy, cell lineages, biochemistry and behavior. There is now undoubtedly more accumulated knowledge on C. elegans than on any other multicellular creature. It is also the largest metazoan which can be continuously cultured on a chemically defined medium, and though most studies have proceeded on undefined media or in monoxenic culture (utilizing a bacterium as a food source), this property can be exploited for precise nutritional studies. In regard to aging studies, the question of relevance of aging in the nematode to that in mammals has been answered in respect to some parameters which characterize senescence in humans, and further study will define other features of aging which are common to all metazoa. In practical terms, this means that test which require 24-36 months to rear an aged rat for evaluation of a pharmaceutical, can potentially be accomplished in 21 days using the nematode. The paper emphasizes that the use of the C. elegans system as a primary screen for candidate compounds to intervene in the aging process can save time, effort and money, while
-
[
WormBook,
2005]
Sex determination was a founding topic of C. elegans research. After three decades of research, a complex signal transduction pathway with multiple layers of regulation has been elucidated. This pathway links karyotype to phenotype by coordinating the development of sexually dimorphic tissues. In this article, this pathway is placed in two broader contexts. The first is that of nematodes and animals in general. The important role of C. elegans studies in revealing the first universally conserved component of metazoan sex determination is discussed, as is the role of cooption of genes into the sex determination and dosage compensation pathways. The second context is that of a subset of more closely related species, with emphasis on other members of the genus Caenorhabditis. Studies reviewed here have determined the gene-level conservation of the known pathway and the relative rates of molecular evolution in conserved components, and made substantial progress in the manipulation of gene activity in non- elegans species. Special attention is paid to the origins of hermaphroditism, which evolved from gonochorism through germline-specific changes in sex determination. Recent studies suggest that the most rapidly evolving aspects of sex determination are germline functions related to evolutionary shifts in mating systems, while somatic sex determination is relatively conservative. From all of these studies, a picture emerges in which C. elegans utilizes an intriguing mixture of general and species-specific genes and regulatory mechanisms.
-
Programmed cell death is a common cell fate in most if not all multicellular organisms. Apoptosis, which will be used as a synonym for programmed cell death throughout this chapter, occurs extensively during development as well as during later life. The development of the nematode worm Caenorhabditis elegans provides a good example of the extensive use of programmed cell death.
-
[
WormBook,
2007]
The intestine is one of the major organs in C. elegans and is largely responsible for food digestion and assimilation as well as the synthesis and storage of macromolecules. In addition, the intestine is emerging as a powerful experimental system in which to study such universal biological phenomena as vesicular trafficking, biochemical clocks, stress responses and aging. The present chapter describes some of these many and varied properties of the C. elegans intestine: the embryonic cell lineage, intestine morphogenesis, structure and physiology of the intestinal cell and, finally, the transcription factor network controlling intestine development and function.
-
[
WormBook,
2005]
Nematodes are the most abundant type of animal on earth, and live in hot springs, polar ice, soil, fresh and salt water, and as parasites of plants, vertebrates, insects, and other nematodes. This extraordinary ability to adapt, which hints at an underlying genetic plasticity, has long fascinated biologists. The fully sequenced genomes of Caenorhabditis elegans and Caenorhabditis briggsae, and ongoing sequencing projects for eight other nematodes, provide an exciting opportunity to investigate the genomic changes that have enabled nematodes to invade many different habitats. Analyses of the C. elegans and C. briggsae genomes suggest that these include major changes in gene content; as well as in chromosome number, structure and size. Here I discuss how the data set of ten genomes will be ideal for tackling questions about nematode evolution, as well as questions relevant to all eukaryotes.