Literature DB >> 18925374

Evolutionary and functional diversity of coronin proteins.

Charles-Peter Xavier1, Ludwig Eichinger, M Pilar Fernandez, Reginald O Morgan, Christoph S Clemen.   

Abstract

This chapter discusses various aspects of coronin phylogeny, structure and function that are of specific interest. Two subfamilies of ancient coronins of unicellular pathogens such as Entamoeba, Trypanosoma, Leishmania and Acanthamoeba as well as of Plasmodium, Babesia, and Trichomonas are presented in the first two sections. Their coronins generally bind to F-actin and apparently are involved in proliferation, locomotion and phagocytosis. However, there are so far no studies addressing a putative role of coronin in the virulence of these pathogens. The following section delineates genetic anomalies like the chimeric coronin-fusion products with pelckstrin homology and gelsolin domains that are found in amoeba. Moreover, most nonvertebrate metazoa appear to encode CRN8, CRN9 and CRN7 representatives (for these coronin symbols see Chapter 2), but in e.g., Drosophila melanogaster and Caenorhabditis elegans a CRN9 is missing. The forth section deals with the evolutionary expansion of vertebrate coronins. Experimental data on the F-actin binding CRN2 of Xenopus (Xcoronin) including a Cdc42/Rac interactive binding (CRIB) motif that is also present in other members of the coronin protein family are discussed. Xenopus laevis represents a case for the expansion of the seven vertebrate coronins due to tetraploidization events. Other examples for a change in the number of coronin paralogs are zebrafish and birds, but (coronin) gene duplication events also occurred in unicellular protozoa. The fifth section of this chapter briefly summarizes three different cellular processes in which CRN4/CORO1A is involved, namely actin-binding, superoxide generation and Ca(2+)-signaling and refers to the largely unexplored mammalian coronins CRN5/CORO2A and CRN6/CORO2B, the latter binding to vinculin. The final section discusses how, by unveiling the aspects of coronin function in organisms reported so far, one can trace a remarkable evolution and diversity in their individual roles anticipating a rather complex and intricate involvement of coronins in a variety of cellular processes.

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Year:  2008        PMID: 18925374     DOI: 10.1007/978-0-387-09595-0_9

Source DB:  PubMed          Journal:  Subcell Biochem        ISSN: 0306-0225


  15 in total

Review 1.  Unraveling the enigma: progress towards understanding the coronin family of actin regulators.

Authors:  Keefe T Chan; Sarah J Creed; James E Bear
Journal:  Trends Cell Biol       Date:  2011-06-01       Impact factor: 20.808

2.  Role of coronin 1B in PDGF-induced migration of vascular smooth muscle cells.

Authors:  Holly C Williams; Alejandra San Martín; Candace M Adamo; Bonnie Seidel-Rogol; Lily Pounkova; Srinivasan Raju Datla; Bernard Lassègue; James E Bear; Kathy Griendling
Journal:  Circ Res       Date:  2012-05-22       Impact factor: 17.367

Review 3.  The expanding spectrum of human coronin 1A deficiency.

Authors:  Despina Moshous; Jean-Pierre de Villartay
Journal:  Curr Allergy Asthma Rep       Date:  2014-12       Impact factor: 4.806

4.  Coro1B and Coro1C regulate lamellipodia dynamics and cell motility by tuning branched actin turnover.

Authors:  Zayna T King; Mitchell T Butler; Max A Hockenberry; Bhagawat C Subramanian; Priscila F Siesser; David M Graham; Wesley R Legant; James E Bear
Journal:  J Cell Biol       Date:  2022-06-03       Impact factor: 8.077

5.  A Cdc42- and Rac-interactive binding (CRIB) domain mediates functions of coronin.

Authors:  Karthic Swaminathan; Annette Müller-Taubenberger; Jan Faix; Francisco Rivero; Angelika A Noegel
Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-17       Impact factor: 11.205

6.  CRN2 enhances the invasiveness of glioblastoma cells.

Authors:  Anja Ziemann; Simon Hess; Ridhirama Bhuwania; Stefan Linder; Peter Kloppenburg; Angelika A Noegel; Christoph S Clemen
Journal:  Neuro Oncol       Date:  2013-02-14       Impact factor: 12.300

7.  A holistic phylogeny of the coronin gene family reveals an ancient origin of the tandem-coronin, defines a new subfamily, and predicts protein function.

Authors:  Christian Eckert; Björn Hammesfahr; Martin Kollmar
Journal:  BMC Evol Biol       Date:  2011-09-25       Impact factor: 3.260

8.  Coronin-1C Protein and Caveolin Protein Provide Constitutive and Inducible Mechanisms of Rac1 Protein Trafficking.

Authors:  Rosalind C Williamson; Christopher A M Cowell; Thomas Reville; James A Roper; Thomas C S Rendall; Mark D Bass
Journal:  J Biol Chem       Date:  2015-04-29       Impact factor: 5.157

9.  Porcine coronin 1A contributes to nuclear factor-kappa B (NF-κB) inactivation during Haemophilus parasuis infection.

Authors:  Chong Liu; Yang Wang; Hengling Zhang; Shuang Cheng; Catherine Charreyre; Jean Christophe Audonnet; Pin Chen; Qigai He
Journal:  PLoS One       Date:  2014-08-05       Impact factor: 3.240

10.  In vitro infectivity and differential gene expression of Leishmania infantum metacyclic promastigotes: negative selection with peanut agglutinin in culture versus isolation from the stomodeal valve of Phlebotomus perniciosus.

Authors:  Pedro J Alcolea; Ana Alonso; María A Degayón; Mercedes Moreno-Paz; Maribel Jiménez; Ricardo Molina; Vicente Larraga
Journal:  BMC Genomics       Date:  2016-05-20       Impact factor: 3.969

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