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[
1982]
Much of this meeting is devoted to the study of multi-gene families and the differential expression of various members during muscle development. Structural analysis of myosin and then other muscle proteins by peptide mapping and amino acid sequencing first suggested that these isoforms are the products of different genes. The use of antibodies specific to distinct structural gene products has permitted detailed investigations of myosin structure, biosynthesis and degradation, and cellular location as muscle development proceeds. The small nematode, Caenorhabditis elegans, is a laboratory animal which offers genetic dissection and manipulation as tools in deciphering of gene regulation in terms of specific protein synthesis during muscle development. The examination of specific mutants by protein chemistry and immunochemistry has already proved a powerful comination in many fields.
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The world of modern biology is unified by genetics. Genetic approaches have the ability to transcend species and provide cross-links between fields for several reasons. First, is the fact that all species are evolutionarily related. Thus, distinct species have similar gene function, and DNA sequence homology can be found between even distantly related species. Indeed, DNA sequence homology is used as a metric device to determine evolutionary relationships among species. Second, molecular genetic manipulation changes both the genotype and phenotype of an organism. Such manipulations represent an extremely fine-scale tool for dissection of the underlying biochemistry, physiology, anatomy, and development of an individual species. Because virtually any gene can be manipulated at will in many species, a dedicated approach can lead to an unraveling of the relationship between genotype and phenotype for almost any gene in these species.....
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[
WormBook,
2006]
Physiological methods entered the world of C. elegans, a model system used for many years to study development and a plethora of biological processes mainly employing genetic, molecular and anatomical techniques. One of the methods introduced by physiologists is the use of Xenopus oocytes for expression of C. elegans ion channels. Oocytes of the South African frog Xenopus laevis are used widely for the expression of mammalian channels and transporters contributing to numerous discoveries in these fields. They now promise to aid C. elegans researchers in deciphering mechanisms of channels function and regulation with implications for mammalian patho-physiology. Heterologous cRNA can be easily injected into Xenopus oocytes and translated proteins can be studied using several techniques including electrophysiology, immunocytochemistry and protein biochemistry. This chapter will focus on techniques used for oocyte preparation and injection, and will give a brief overview of specific methods. Limitations of the use of Xenopus oocytes will be also discussed.
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[
Methods Cell Biol,
1995]
Behavioral plasticity is the ability of organisms to modify their behavior over time, based on their experience, and is thus critical to the survival of any organism in a changing environment. It allows organisms to adapt to new surroundings and to take better advantage of novel situational variables they may encounter. It is therefore an extremely important ability, and it has attracted much research attention in innumberable organisms and across several disciplines. Much of the research on plasticity has been characterized by an attempt to integrate information and expertise from a number of these different disciplines within selected invertebrate organisms. Researchers from a variety of fields, including psychology, physiology, biochemistry, genetics, neurobiology, and molecular biology, have been uniting in an effort to investigate "simple system" in which these approaches are being combined and focused on the general goal of elucidating the cellular, molecular, and genetic basis of behavioral plasticity. These simple system approaches have led to considerable progress in our understanding of the mechanisms underlying adaptive behaviors. The general strategy of such approaches is to try to identify the genes, molecules, channels, ion currents, cells, and neural circuits underlying some form of plasticity and then determine the precise nature of their respective roles in producing behavior...
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[
WormBook,
2005]
The use of Wnt ligands for signaling between cells is a conserved feature of metazoan development. Activation of Wnt signal transduction pathways upon ligand binding can regulate diverse processes including cell proliferation, migration, polarity, differentiation and axon outgrowth. A ''canonical'' Wnt signaling pathway has been elucidated in vertebrate and invertebrate model systems. In the canonical pathway, Wnt binding leads to the stabilization of the transcription factor beta-catenin, which enters the nucleus to regulate Wnt pathway target genes. However, Wnt binding also acts through beta-catenin-independent, noncanonical pathways, such as the planar cell polarity (PCP) pathway and a pathway involving Ca 2+ signaling. This chapter examines our current understanding of Wnt signaling and Wnt-mediated processes in the nematode C. elegans. Like other species, the C. elegans genome encodes multiple genes for Wnt ligands (five) and Wnt receptors (four frizzleds, one Ryk/Derailed). Unlike vertebrates or Drosophila, the C. elegans genome encodes three beta-catenin genes, which appear to have distinct functions in Wnt signaling and cell adhesion. Canonical Wnt signaling clearly exists in C. elegans, utilizing the beta-catenin BAR-1 . However, a noncanonical pathway utilizing the beta-catenin WRM-1 also exists, and to date a similar pathway has not been described in other species. Evidence for beta-catenin independent noncanonical Wnt signaling is currently limited. The role of Wnt signaling in over a dozen C. elegans developmental processes, including the regulation of cell fate, polarity and migration, is described.