980 resultados para William L. Clements Library
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Vaccinia uses actin-based motility for virion movement in host cells, but the specific protein components have yet to be defined. A cardinal feature of Listeria and Shigella actin-based motility is the involvement of vasodilator-stimulated phosphoprotein (VASP). This essential adapter recognizes and binds to actin-based motility 1 (ABM-1) consensus sequences [(D/E)FPPPPX(D/E), X = P or T] contained in Listeria ActA and in the p90 host-cell vinculin fragment generated by Shigella infection. VASP, in turn, provides the ABM-2 sequences [XPPPPP, X = G, P, L, S, A] for binding profilin, an actin-regulatory protein that stimulates actin filament assembly. Immunolocalization using rabbit anti-VASP antibody revealed that VASP concentrates behind motile virions in HeLa cells. Profilin was also present in these actin-rich rocket tails, and microinjection of 10 μM (intracellular) ABM-2 peptide (GPPPPP)3 blocked vaccinia actin-based motility. Vinculin did not colocalize with VASP on motile virions and remained in focal adhesion contacts; however, another ABM-1-containing host protein, zyxin, was concentrated at the rear of motile virions. We also examined time-dependent changes in the location of these cytoskeletal proteins during vaccinia infection. VASP and zyxin were redistributed dramatically several hours before the formation of actin rocket tails, concentrating in the viral factories of the perinuclear cytoplasm. Our findings underscore the universal involvement of ABM-1 and ABM-2 docking sites in actin-based motility of Listeria, Shigella, and now vaccinia.
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In many organisms, there are multiple isoforms of cytoplasmic dynein heavy chains, and division of labor among the isoforms would provide a mechanism to regulate dynein function. The targeted disruption of somatic genes in Tetrahymena thermophila presents the opportunity to determine the contributions of individual dynein isoforms in a single cell that expresses multiple dynein heavy chain genes. Substantial portions of two Tetrahymena cytoplasmic dynein heavy chain genes were cloned, and their motor domains were sequenced. Tetrahymena DYH1 encodes the ubiquitous cytoplasmic dynein Dyh1, and DYH2 encodes a second cytoplasmic dynein isoform, Dyh2. The disruption of DYH1, but not DYH2, resulted in cells with two detectable defects: 1) phagocytic activity was inhibited, and 2) the cells failed to distribute their chromosomes correctly during micronuclear mitosis. In contrast, the disruption of DYH2 resulted in a loss of regulation of cell size and cell shape and in the apparent inability of the cells to repair their cortical cytoskeletons. We conclude that the two dyneins perform separate tasks in Tetrahymena.
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To assess the regional effects of glaciation on sedimentation in the Atlantic Ocean we compare sediment types, distributions, and rates between Recent (core top) and last glacial maximum (LGM: ~18,000 years B.P.) stratigraphic levels. Based upon smear slides and carbonate analyses in 178 cores we find that glacial age carbonate content is generally lower than Recent. During both the Recent and LGM, carbonate content shows an east/west asymmetry with western basins exhibiting lower carbonate values. Input of ice-rafted detritus into the North Atlantic during LGM time interrupts this topographic control on carbonate distribution considerably farther south than at present; in the South Atlantic this effect is minor. Comparison of LGM and Recent sediment distributions indicates that the LGM seafloor was dominated by biogenic oozes, calcareous clays, and clays, while the Recent is dominated by biogenic oozes and marls. Coarse-grained detritus is much more prevalent in LGM sediments, derived not only from glacial input but also from fluvial and aeolian sources. Sedimentation rates, calculated from LGM to Recent sediment thickness in cores, are <4 cm/1000 yr for most of the ocean. Higher rates are typical of the continental margin off the Amazon River, the North American Basin, and a small region off west equatorial Africa.
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At head of title: U.S. Department of Commerce. R.P. Lamont, secretary. Bureau of Foreign and Domestic Commerce. William L. Cooper, director.
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Oct. 1978.
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Mode of access: Internet.
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Mode of access: Internet.
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Issued April 1977.
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"April 1980"--Cover.
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Mode of access: Internet.
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Mode of access: Internet.