Literature DB >> 26462928

Study of model systems to test the potential function of Artemia group 1 late embryogenesis abundant (LEA) proteins.

Alden H Warner1, Zhi-Hao Guo2, Sandra Moshi2, John W Hudson2, Anna Kozarova2.   

Abstract

Embryos of the brine shrimp, Artemia franciscana, are genetically programmed to develop either ovoviparously or oviparously depending on environmental conditions. Shortly upon their release from the female, oviparous embryos enter diapause during which time they undergo major metabolic rate depression while simultaneously synthesize proteins that permit them to tolerate a wide range of stressful environmental events including prolonged periods of desiccation, freezing, and anoxia. Among the known stress-related proteins that accumulate in embryos entering diapause are the late embryogenesis abundant (LEA) proteins. This large group of intrinsically disordered proteins has been proposed to act as molecular shields or chaperones of macromolecules which are otherwise intolerant to harsh conditions associated with diapause. In this research, we used two model systems to study the potential function of the group 1 LEA proteins from Artemia. Expression of the Artemia group 1 gene (AfrLEA-1) in Escherichia coli inhibited growth in proportion to the number of 20-mer amino acid motifs expressed. As well, clones of E. coli, transformed with the AfrLEA-1 gene, expressed multiple bands of LEA proteins, either intrinsically or upon induction with isopropyl-β-thiogalactoside (IPTG), in a vector-specific manner. Expression of AfrLEA-1 in E. coli did not overcome the inhibitory effects of high concentrations of NaCl and KCl but modulated growth inhibition resulting from high concentrations of sorbitol in the growth medium. In contrast, expression of the AfrLEA-1 gene in Saccharomyces cerevisiae did not alter the growth kinetics or permit yeast to tolerate high concentrations of NaCl, KCl, or sorbitol. However, expression of AfrLEA-1 in yeast improved its tolerance to drying (desiccation) and freezing. Under our experimental conditions, both E. coli and S. cerevisiae appear to be potentially suitable hosts to study the function of Artemia group 1 LEA proteins under environmentally stressful conditions.

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Year:  2016        PMID: 26462928      PMCID: PMC4679747          DOI: 10.1007/s12192-015-0647-3

Source DB:  PubMed          Journal:  Cell Stress Chaperones        ISSN: 1355-8145            Impact factor:   3.667


  57 in total

Review 1.  Molecular chaperones, stress resistance and development in Artemia franciscana.

Authors:  Thomas H MacRae
Journal:  Semin Cell Dev Biol       Date:  2003-10       Impact factor: 7.727

Review 2.  Gene expression, metabolic regulation and stress tolerance during diapause.

Authors:  Thomas H MacRae
Journal:  Cell Mol Life Sci       Date:  2010-03-07       Impact factor: 9.261

3.  Functional characterization of selected LEA proteins from Arabidopsis thaliana in yeast and in vitro.

Authors:  Nghiem X Dang; Antoneta V Popova; Michaela Hundertmark; Dirk K Hincha
Journal:  Planta       Date:  2014-05-20       Impact factor: 4.116

4.  Group 1 LEA proteins contribute to the desiccation and freeze tolerance of Artemia franciscana embryos during diapause.

Authors:  Jantina Toxopeus; Alden H Warner; Thomas H MacRae
Journal:  Cell Stress Chaperones       Date:  2014-05-21       Impact factor: 3.667

5.  The wheat LEA protein Em functions as an osmoprotective molecule in Saccharomyces cerevisiae.

Authors:  G A Swire-Clark; W R Marcotte
Journal:  Plant Mol Biol       Date:  1999-01       Impact factor: 4.076

6.  Genetic analysis of desiccation tolerance in Sachharomyces cerevisiae.

Authors:  Dean Calahan; Maitreya Dunham; Chris DeSevo; Douglas E Koshland
Journal:  Genetics       Date:  2011-08-11       Impact factor: 4.562

7.  Quantification of cellular protein expression and molecular features of group 3 LEA proteins from embryos of Artemia franciscana.

Authors:  Leaf C Boswell; Daniel S Moore; Steven C Hand
Journal:  Cell Stress Chaperones       Date:  2013-09-06       Impact factor: 3.667

Review 8.  Multifarious roles of intrinsic disorder in proteins illustrate its broad impact on plant biology.

Authors:  Xiaolin Sun; Erik H A Rikkerink; William T Jones; Vladimir N Uversky
Journal:  Plant Cell       Date:  2013-01-29       Impact factor: 11.277

9.  Initiation of translation in bacteria by a structured eukaryotic IRES RNA.

Authors:  Timothy M Colussi; David A Costantino; Jianyu Zhu; John Paul Donohue; Andrei A Korostelev; Zane A Jaafar; Terra-Dawn M Plank; Harry F Noller; Jeffrey S Kieft
Journal:  Nature       Date:  2015-02-04       Impact factor: 49.962

10.  The small heat shock protein p26 aids development of encysting Artemia embryos, prevents spontaneous diapause termination and protects against stress.

Authors:  Allison M King; Thomas H MacRae
Journal:  PLoS One       Date:  2012-08-27       Impact factor: 3.240

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  3 in total

1.  High-throughput mass spectrometry analysis revealed a role for glucosamine in potentiating recovery following desiccation stress in Chironomus.

Authors:  Leena Thorat; Dasharath Oulkar; Kaushik Banerjee; Sushama M Gaikwad; Bimalendu B Nath
Journal:  Sci Rep       Date:  2017-06-16       Impact factor: 4.379

2.  Insights on Structure and Function of a Late Embryogenesis Abundant Protein from Amaranthus cruentus: An Intrinsically Disordered Protein Involved in Protection against Desiccation, Oxidant Conditions, and Osmotic Stress.

Authors:  Alma L Saucedo; Eric E Hernández-Domínguez; Luis A de Luna-Valdez; Angel A Guevara-García; Abraham Escobedo-Moratilla; Esaú Bojorquéz-Velázquez; Federico Del Río-Portilla; Daniel A Fernández-Velasco; Ana P Barba de la Rosa
Journal:  Front Plant Sci       Date:  2017-04-07       Impact factor: 5.753

3.  Functional and Conformational Plasticity of an Animal Group 1 LEA Protein.

Authors:  Brett Janis; Clinton Belott; Tyler Brockman; Michael A Menze
Journal:  Biomolecules       Date:  2022-03-10
  3 in total

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