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      Actin Dynamics Couples Extracellular Signals to the Mobility and Molecular Stability of Telomeres

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          Abstract

          Genome regulatory programs such as telomere functioning require extracellular signals to be transmitted from the microenvironment to the nucleus and chromatin. Although the cytoskeleton has been shown to directly transmit stresses, we show that the intrinsically dynamic nature of the actin cytoskeleton is important in relaying extracellular signals to telomeres. Interestingly, this mechanical pathway not only transmits physical stimuli but also chemical stimuli. The cytoskeletal network continuously reorganizes and applies dynamic forces on the nucleus and feeds into the regulation of telomere dynamics. We further found that distal telomeres are mechanically coupled in a length- and timescale-dependent manner and identified nesprin 2G as well as lamin A/C as being essential to regulate their translational dynamics. Finally, we demonstrated that such mechanotransduction events impinge on the binding dynamics of critical telomere binding proteins. Our results highlight an overarching physical pathway that regulates positional and molecular stability of telomeres.

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          Most cited references41

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          How telomeres solve the end-protection problem.

          The ends of eukaryotic chromosomes have the potential to be mistaken for damaged or broken DNA and must therefore be protected from cellular DNA damage response pathways. Otherwise, cells might permanently arrest in the cell cycle, and attempts to "repair" the chromosome ends would have devastating consequences for genome integrity. This end-protection problem is solved by protein-DNA complexes called telomeres. Studies of mammalian cells have recently uncovered the mechanism by which telomeres disguise the chromosome ends. Comparison to unicellular eukaryotes reveals key differences in the DNA damage response systems that inadvertently threaten chromosome ends. Telomeres appear to be tailored to these variations, explaining their variable structure and composition.
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            Signaling through scaffold, anchoring, and adaptor proteins.

            The process by which extracellular signals are relayed from the plasma membrane to specific intracellular sites is an essential facet of cellular regulation. Many signaling pathways do so by altering the phosphorylation state of tyrosine, serine, or threonine residues of target proteins. Recently, it has become apparent that regulatory mechanisms exist to influence where and when protein kinases and phosphatases are activated in the cell. The role of scaffold, anchoring, and adaptor proteins that contribute to the specificity of signal transduction events by recruiting active enzymes into signaling networks or by placing enzymes close to their substrates is discussed.
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              Single-molecule speckle analysis of actin filament turnover in lamellipodia.

              Lamellipodia are thin, veil-like extensions at the edge of cells that contain a dynamic array of actin filaments. We describe an approach for analyzing spatial regulation of actin polymerization and depolymerization in vivo in which we tracked single molecules of actin fused to the green fluorescent protein. Polymerization and the lifetime of actin filaments in lamellipodia were measured with high spatial precision. Basal polymerization and depolymerization occurred throughout lamellipodia with largely constant kinetics, and polymerization was promoted within one micron of the lamellipodium tip. Most of the actin filaments in the lamellipodium were generated by polymerization away from the tip.
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                Author and article information

                Contributors
                Journal
                Biophys J
                Biophys. J
                Biophysical Journal
                The Biophysical Society
                0006-3495
                1542-0086
                02 October 2018
                29 August 2018
                : 115
                : 7
                : 1166-1179
                Affiliations
                [1 ]Mechanobiology Institute, National University of Singapore, Singapore
                [2 ]Department of Biological Sciences, National University of Singapore, Singapore
                [3 ]Institute of Molecular Oncology, Italian Foundation for Cancer Research, Milan, Italy
                Author notes
                []Corresponding author shiva.gvs@ 123456gmail.com
                Article
                S0006-3495(18)30983-4
                10.1016/j.bpj.2018.08.029
                6170704
                30224051
                772372a5-a8df-4a10-a830-8a3e88f67c29
                © 2018 Biophysical Society.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 23 March 2018
                : 15 August 2018
                Categories
                Nucleic Acids and Genome Biophysics

                Biophysics
                Biophysics

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