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      Flexible tethering of primase and DNA Pol α in the eukaryotic primosome

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          Abstract

          The Pol α/primase complex or primosome is the primase/polymerase complex that initiates nucleic acid synthesis during eukaryotic replication. Within the primosome, the primase synthesizes short RNA primers that undergo limited extension by Pol α. The resulting RNA–DNA primers are utilized by Pol δ and Pol ε for processive elongation on the lagging and leading strands, respectively. Despite its importance, the mechanism of RNA–DNA primer synthesis remains poorly understood. Here, we describe a structural model of the yeast primosome based on electron microscopy and functional studies. The 3D architecture of the primosome reveals an asymmetric, dumbbell-shaped particle. The catalytic centers of primase and Pol α reside in separate lobes of high relative mobility. The flexible tethering of the primosome lobes increases the efficiency of primer transfer between primase and Pol α. The physical organization of the primosome suggests that a concerted mechanism of primer hand-off between primase and Pol α would involve coordinated movements of the primosome lobes. The first three-dimensional map of the eukaryotic primosome at 25 Å resolution provides an essential structural template for understanding initiation of eukaryotic replication.

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          Most cited references30

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          DNA primases.

          DNA primases are enzymes whose continual activity is required at the DNA replication fork. They catalyze the synthesis of short RNA molecules used as primers for DNA polymerases. Primers are synthesized from ribonucleoside triphosphates and are four to fifteen nucleotides long. Most DNA primases can be divided into two classes. The first class contains bacterial and bacteriophage enzymes found associated with replicative DNA helicases. These prokaryotic primases contain three distinct domains: an amino terminal domain with a zinc ribbon motif involved in binding template DNA, a middle RNA polymerase domain, and a carboxyl-terminal region that either is itself a DNA helicase or interacts with a DNA helicase. The second major primase class comprises heterodimeric eukaryotic primases that form a complex with DNA polymerase alpha and its accessory B subunit. The small eukaryotic primase subunit contains the active site for RNA synthesis, and its activity correlates with DNA replication during the cell cycle.
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            Disentangling conformational states of macromolecules in 3D-EM through likelihood optimization.

            Although three-dimensional electron microscopy (3D-EM) permits structural characterization of macromolecular assemblies in distinct functional states, the inability to classify projections from structurally heterogeneous samples has severely limited its application. We present a maximum likelihood-based classification method that does not depend on prior knowledge about the structural variability, and demonstrate its effectiveness for two macromolecular assemblies with different types of conformational variability: the Escherichia coli ribosome and Simian virus 40 (SV40) large T-antigen.
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              Structural basis of high fidelity DNA synthesis by yeast DNA polymerase delta

              DNA polymerase δ (Polδ) is a high fidelity polymerase that plays a central role in replication from yeast to humans. We present here the crystal structure of the catalytic subunit of yeast Polδ in ternary complex with a template-primer and an incoming nucleotide. The structure, determined at 2.0Å resolution, catches the enzyme in the act of replication. The structure reveals how the polymerase and exonuclease domains are juxtaposed relative to each other and how a correct nucleotide is selected and incorporated. The structure also reveals the “sensing” interactions near the primer terminus that signal a switch from the polymerizing to the editing mode. Taken together, the structure provides a chemical basis for the bulk of DNA synthesis in eukaryotic cells and a framework for understanding the effects of mutations in Polδ̣ that cause cancers.
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                Author and article information

                Journal
                Nucleic Acids Res
                nar
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                October 2011
                October 2011
                28 June 2011
                28 June 2011
                : 39
                : 18
                : 8187-8199
                Affiliations
                1Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Ramiro de Maetzu 9, 28040 Madrid, Spain, 2Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1GA, UK and 3University of California, 742 Stanley Hall, MS 3220, Berkeley, CA 94720-3220, USA
                Author notes
                *To whom correspondence should be addressed. Tel: +34 918373112 (Ext. 4446); Fax: +34 915360432; Email: ollorca@ 123456cib.csic.es
                Correspondence may also be addressed to Luca Pellegrini. Tel: +0044 1223 760469; Fax: +0044 1223 766002; Email: lp212@ 123456cam.ac.uk

                The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.

                Present addresseses: Rafael Núñez-Ramírez, Instituto de Estructura de la Materia, CSIC, Serrano 113bis, 28006 Madrid, Spain.

                Sebastian Klinge, Institut für Molekularbiologie und Biophysik, ETH Zurich, CH-8093, Switzerland.

                Ludovic Sauguet, Département de Biologie Structurale et Chimie, Institut Pasteur, 75724 Paris CEDEX 15, France.

                Begoña García-Alvarez, Universidad Complutense de Madrid, Madrid, Spain.

                Article
                gkr534
                10.1093/nar/gkr534
                3185431
                21715379
                15f24362-572b-4111-a58f-c5ef1001ee79
                © The Author(s) 2011. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 14 April 2011
                : 20 May 2011
                : 12 June 2011
                Page count
                Pages: 13
                Categories
                Structural Biology

                Genetics
                Genetics

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