Multiple Mouse Chromosomal Loci for Dynein-Based Motility
Multiple Mouse Chromosomal Loci for Dynein-Based Motility
Dyneins are multisubunit mechanochemical enzymes capable of interacting with microtubules to generate force. Axonemal dyneins produce the motive force for ciliary and flagellar beating by inducing sliding between adjacent microtubules within the axoneme. Cytoplasmic dyneins translocate membranous organelles and chromosomes toward the minus ends of cytoplasmic microtubules. Dynactin is an accessory complex implicated in tethering cytoplasmic dynein to membranous organelles and mitotic kinetochores. In the studies described here, we have identified a number of new dynein genes and determined their mouse chromosomal locations by interspecific backcross analysis. We have also mapped several dynein and dynactin genes cloned previously. Our studies provide the first comprehensive attempt to map dynein and dynactin genes in mammals and provide a basis for the further analysis of dynein function in development and disease.
- University of Massachusetts Medical School United States
- Worcester Foundation for Biomedical Research United States
Messenger, Molecular Sequence Data, *Chromosome Mapping, Crosses, Inbred C57BL, Dynein ATPase, Mice, Genetic, Medicine and Health Sciences, Animals, Amino Acid Sequence, RNA, Messenger, Polymorphism, Cloning, Molecular, Crosses, Genetic, *Microtubule-Associated Proteins, Molecular, Life Sciences, Chromosome Mapping, Dyneins, Dynactin Complex, Rats, Mice, Inbred C57BL, Muridae, Restriction Fragment Length, Genes, Organ Specificity, Microtubule Proteins, RNA, Microtubule-Associated Proteins, Polymorphism, Restriction Fragment Length, Cloning
Messenger, Molecular Sequence Data, *Chromosome Mapping, Crosses, Inbred C57BL, Dynein ATPase, Mice, Genetic, Medicine and Health Sciences, Animals, Amino Acid Sequence, RNA, Messenger, Polymorphism, Cloning, Molecular, Crosses, Genetic, *Microtubule-Associated Proteins, Molecular, Life Sciences, Chromosome Mapping, Dyneins, Dynactin Complex, Rats, Mice, Inbred C57BL, Muridae, Restriction Fragment Length, Genes, Organ Specificity, Microtubule Proteins, RNA, Microtubule-Associated Proteins, Polymorphism, Restriction Fragment Length, Cloning
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