Two P1B-1-ATPases of Amanita strobiliformis With Distinct Properties in Cu/Ag Transport

. 2018 ; 9 () : 747. [epub] 20180423

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid29740406

As we have shown previously, the Cu and Ag concentrations in the sporocarps of Ag-hyperaccumulating Amanita strobiliformis are correlated, and both metals share the same uptake system and are sequestered by the same metallothioneins intracellularly. To further improve our knowledge of the Cu and Ag handling in A. strobiliformis cells, we searched its transcriptome for the P1B-1-ATPases, recognizing Cu+ and Ag+ for transport. We identified transcripts encoding 1097-amino acid (AA) AsCRD1 and 978-AA AsCCC2, which were further subjected to functional studies in metal sensitive Saccharomyces cerevisiae. The expression of AsCRD1 conferred highly increased Cu and Ag tolerance to metal sensitive yeasts in which the functional AsCRD1:GFP (green fluorescent protein) fusion localized exclusively to the tonoplast, indicating that the AsCRD1-mediated Cu and Ag tolerance was a result of vacuolar sequestration of the metals. Increased accumulation of AsCRD1 transcripts observed in A. strobiliformis mycelium upon the treatments with Cu and Ag (8.7- and 4.5-fold in the presence of 5 μM metal, respectively) supported the notion that AsCRD1 can be involved in protection of the A. strobiliformis cells against the toxicity of both metals. Neither Cu nor Ag affected the levels of AsCCC2 transcripts. Heterologous expression of AsCCC2 in mutant yeasts did not contribute to Cu tolerance, but complemented the mutant genotype of the S. cerevisiae ccc2Δ strain. Consistent with the role of the yeast Ccc2 in the trafficking of Cu from cytoplasm to nascent proteins via post-Golgi, the GFP fluorescence in AsCCC2-expressing ccc2Δ yeasts localized among Golgi-like punctate foci within the cells. The AsCRD1- and AsCCC2-associated phenotypes were lost in yeasts expressing mutant transporter variants in which a conserved phosphorylation/dephosphorylation site was altered. Altogether, the data support the roles of AsCRD1 and AsCCC2 as genuine P1B-1-ATPases, and indicate their important functions in the removal of toxic excess of Cu and Ag from the cytoplasm and charging the endomembrane system with Cu, respectively.

Zobrazit více v PubMed

Adle D. J., Sinani D., Kim H., Lee J. (2007). A cadmium-transporting P1B-type ATPase in yeast PubMed DOI PMC

Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. (1990). Basic local alignment search tool. PubMed DOI

Antsotegi-Uskola M., Markina-Iñarrairaegui A., Ugalde U. (2017). Copper resistance in PubMed DOI PMC

Argüello J. M., Eren E., González-Guerrero M. (2007). The structure and function of heavy metal transport P-1B-ATPases. PubMed DOI

Bashir K., Rasheed S., Kobayashi T., Seki M., Nishizawa N. K. (2016). Regulating subcellular metal homeostasis: the key to crop improvement. PubMed DOI PMC

Bellion M., Courbot M., Jacob C., Guinet F., Blaudez D., Chalot M. (2007). Metal induction of a Paxillus involutus metallothionein and its heterologous expression in Hebeloma cylindrosporum. PubMed DOI

Beneš V., Hložková K., Matěnová M., Borovička J., Kotrba P. (2016). Accumulation of Ag and Cu in PubMed DOI

Bleackley M. R., MacGillivray R. T. (2011). Transition metal homeostasis: from yeast to human disease. PubMed DOI

Borovička J., Kotrba P., Gryndler M., Mihaljevič M., Řanda Z., Rohovec J., et al. (2010). Bioaccumulation of silver in ectomycorrhizal and saprobic macrofungi from pristine and polluted areas. PubMed DOI

Borovička J., Řanda Z., Jelínek E., Kotrba P., Dunn C. E. (2007). Hyperaccumulation of silver by PubMed DOI

Colpaert J. V., Wevers J. H. L., Krznaric E., Adriaensen K. (2011). How metal-tolerant ecotypes of ectomycorrhizal fungi protect plants from heavy metal pollution. DOI

Courty P. E., Hoegger P. J., Kilaru S., Kohler A., Buée M., Garbaye J., et al. (2009). Phylogenetic analysis, genomic organization, and expression analysis of multi-copper oxidases in the ectomycorrhizal basidiomycete Laccaria bicolor. PubMed DOI

Devirgiliis C., Murgia C., Danscher G., Perozzi G. (2004). Exchangeable zinc ions transiently accumulate in a vesicular compartment in the yeast PubMed DOI

Dobson L., Reményi I., Tusnády G. E. (2015). CCTOP: A Consensus Constrained TOPology prediction web server. PubMed DOI PMC

Ellström M., Shah F., Johansson T., Ahrén D., Persson P., Tunlid A. (2015). The carbon starvation response of the ectomycorrhizal fungus PubMed DOI PMC

Falandysz J., Borovička J. (2013). Macro and trace mineral constituents and radionuclides in mushrooms: health benefits and risks. PubMed DOI PMC

Fomina M., Charnock J., Bowen A. D., Gadd G. M. (2007). X-ray absorption spectroscopy (XAS) of toxic metal mineral transformations by fungi. PubMed DOI

Fu D., Beeler T. J., Dunn T. M. (1995). Sequence, mapping and disruption of CCC2, a gene that cross-complements the Ca PubMed DOI

Füzik T., Ulbrich P., Ruml T. (2014). Efficient mutagenesis independent of ligation (EMILI). PubMed DOI

Gadd G. M., Rhee Y. J., Stephenson K., Wei Z. (2012). Geomycology: metals, actinides and biominerals. PubMed DOI

González-Guerrero M., Melville L. H., Ferrol N., Lott J. N. A., Azcón-Aguilar C., Peterson R. L. (2008). Ultrastructural localization of heavy metals in the extraradical mycelium and spores of the arbuscular mycorrhizal fungus PubMed DOI

Gostinčar C., Muggia L., Grube M. (2012). Polyextremotolerant black fungi: oligotrophism, adaptive potential, and a link to lichen symbioses. PubMed DOI PMC

Hložková K., Matìnová M., Žáčková P., Strnad H., Hršelová H., Hroudová M., et al. (2016). Characterization of three distinct metallothionein genes of the Ag-hyperaccumulating ectomycorrhizal fungus PubMed DOI

Kelley L. A., Mezulis S., Yates C. M., Wass M. N., Sternberg M. J. (2015). The Phyre2 web portal for protein modeling, prediction and analysis. PubMed DOI PMC

Kohler A., Kuo A., Nagy L. G., Morin E., Barry K. W., Buscot F., et al. (2015). Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists. PubMed DOI

Kües U., Rühl M. (2011). Multiple multi-copper oxidase gene families in basidiomycetes - what for? PubMed DOI PMC

La Fontaine S., Mercer J. F. B. (2007). Trafficking of the copper-ATPases, ATP7A and ATP7B: Role in copper homeostasis. PubMed DOI

Li Y., Iqbal M., Zhang Q., Spelt C., Bliek M., Hakvoort H. W. J., et al. (2017). Two Silene vulgaris copper transporters residing in different cellular compartments confer copper hypertolerance by distinct mechanisms when expressed in PubMed DOI

Livak K. J., Schmittgen T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2ΔΔC(T) method. PubMed DOI

Migocka M., Posyniak E., Maciaszczyk-Dziubinska E., Papierniak A., Kosieradzaka A. (2015). Functional and biochemical characterization of cucumber genes encoding two copper ATPases CsHMA5.1 and CsHMA5.2. PubMed DOI PMC

Mijnendonckx K., Leys N., Mahillon J., Silver S., Van Houdt R. (2013). Antimicrobial silver: uses, toxicity and potential for resistance. PubMed DOI

Mumberg D., Müller R., Funk M. (1995). Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds. PubMed DOI

Nevitt T., Öhrvik H., Thiele D. J. (2012). Charting the travels of copper in eukaryotes from yeast to mammals. PubMed DOI PMC

Osobová M., Urban V., Jedelský P. L., Borovička J., Gryndler M., Ruml T., et al. (2011). Three metallothionein isoforms and sequestration of intracellular silver in the hyperaccumulator PubMed DOI

Palmgren M. G., Nissen P. (2011). P-Type ATPases. PubMed DOI

Parisot D., Dufresne M., Veneault C., Laugé R., Langin T. (2002). clap1, a gene encoding a copper-transporting ATPase involved in the process of infection by the phytopathogenic fungus PubMed DOI

Pettersen E. F., Goddard T. D., Huang C. C., Couch G. S., Greenblatt D. M., Meng E. C., et al. (2004). UCSF Chimera - a visualization system for exploratory research and analysis. PubMed DOI

Ramesh G., Podila G. K., Gay G., Marmeisse R., Reddy M. S. (2009). Different patterns of regulation for the copper and cadmium metallothioneins of the ectomycorrhizal fungus PubMed DOI PMC

Reddy M. S., Kour M., Aggarwal S., Ahuja S., Marmeisse R., Fraissinet-Tachet L. (2016). Metal induction of a PubMed DOI

Reddy M. S., Prasanna L., Marmeisse R., Fraissinet-Tachet L. (2014). Differential expression of metallothioneins in response to heavy metals and their involvement in metal tolerance in the symbiotic basidiomycete PubMed DOI

Riggle P. J., Kumamoto C. A. (2000). Role of a PubMed DOI PMC

Rodrigues-Pousada C., Menezes R. A., Pimentel C. (2010). The Yap family and its role in stress response. PubMed DOI

Sácký J., Leonhardt T., Borovička J., Gryndler M., Briksí A., Kotrba P. (2014). Intracellular sequestration of zinc, cadmium and silver in Hebeloma mesophaeum and characterization of its metallothionein genes. PubMed DOI

Saitoh Y., Izumitsu K., Morita A., Tanaka C. (2010). A copper-transporting ATPase BcCCC2 is necessary for pathogenicity of PubMed DOI

Shah F., Nicolás C., Bentzer J., Ellström M., Smits M., Rineau F., et al. (2016). Ectomycorrhizal fungi decompose soil organic matter using oxidative mechanisms adapted from saprotrophic ancestors. PubMed DOI PMC

Smith A. T., Smith K. P., Rosenzweig A. C. (2014). Diversity of the metal-transporting P1B-type ATPases. PubMed DOI PMC

Szczypka M. S., Zhu Z., Silar P., Thiele D. J. (1997). PubMed DOI

Tamai K. T., Gralla E. B., Ellerby L. M., Valentine J. S., Thiele D. J. (1993). Yeast and mammalian metallothioneins functionally substitute for yeast copper-zinc superoxide dismutase. PubMed DOI PMC

Tamura K., Stecher G., Peterson D., Filipski A., Kumar S. (2013). MEGA6: molecular evolutionary genetics analysis version 6.0. PubMed DOI PMC

Thompson J. D., Higgins D. G., Gibson T. J. (1994). CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. PubMed DOI PMC

Walton F. J., Idnurm A., Heitman J. (2005). Novel gene functions required for melanization of the human pathogen PubMed DOI

Webb B., Sali A. (2014). Comparative protein structure modeling using MODELLER. PubMed DOI

Weissman Z., Berdicevsky I., Cavari B. Z., Kornitzer D. (2000). The high copper tolerance of Candida albicans is mediated by a P-type ATPase. PubMed DOI PMC

Yuan D. S., Dancis A., Klausner R. D. (1997). Restriction to copper transport in PubMed DOI

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...