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      Proteins of the ADF/cofilin family: essential regulators of actin dynamics.

      Annual review of cell and developmental biology
      Actin Depolymerizing Factors, Actins, metabolism, Amino Acid Sequence, Animals, Destrin, Evolution, Molecular, Humans, Intracellular Fluid, physiology, Kidney Diseases, pathology, Microfilament Proteins, chemistry, classification, genetics, Molecular Sequence Data, Neurodegenerative Diseases, Williams Syndrome

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          Abstract

          Ubiquitous among eukaryotes, the ADF/cofilins are essential proteins responsible for the high turnover rates of actin filaments in vivo. In vertebrates, ADF and cofilin are products of different genes. Both bind to F-actin cooperatively and induce a twist in the actin filament that results in the loss of the phalloidin-binding site. This conformational change may be responsible for the enhancement of the off rate of subunits at the minus end of ADF/cofilin-decorated filaments and for the weak filament-severing activity. Binding of ADF/cofilin is competitive with tropomyosin. Other regulatory mechanisms in animal cells include binding of phosphoinositides, phosphorylation by LIM kinases on a single serine, and changes in pH. Although vertebrate ADF/cofilins contain a nuclear localization sequence, they are usually concentrated in regions containing dynamic actin pools, such as the leading edge of migrating cells and neuronal growth cones. ADF/cofilins are essential for cytokinesis, phagocytosis, fluid phase endocytosis, and other cellular processes dependent upon actin dynamics.

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