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Book with abstracts from the COST Action 0905 meeting in ... - UMB

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PHYSIOLOGICAL CHARACTERIZATION AND TRANSCRIPTION<br />

ANALYSIS OF TWO ARABIDOPSIS MUTANTS RESISTANT TO CDS<br />

NANOPARTICLES<br />

Marta Marmiroli, Luca Pagano, Maria Luisa Savo Sardaro, Nelson Marmiroli<br />

Department of Environmental Sciences, University of Parma, Parma, Italy. Viale G.P.<br />

Usberti 33/A, 43124 Parma, Italy. Tel: 00390521905687. E-mail: marta.marmiroli@unipr.it<br />

Keywords: Arabidopsis thaliana, CdS nanoparticles, microarray, resistance, transposon<br />

mutation.<br />

Nanoparticles have become widely used materials because of <strong>the</strong>ir unique structural, optic,<br />

electromagnetic and reactive properties. CdS quantum-dots are utilized <strong>in</strong> m<strong>in</strong>iaturised<br />

hardware and optics equipment, <strong>the</strong>y are syn<strong>the</strong>sized through an <strong>in</strong>expensive wet-chemistry<br />

process, and have a diameter of 5 nm. The CdS NPs small size make <strong>the</strong>m particularly prone<br />

to enter <strong>in</strong> human and plant cells, but <strong>the</strong>ir toxicity potential has not been assessed yet. In this<br />

study we screened two mutagenised collections of Arabidopsis thaliana (L.) Heynh, to<br />

identify CdS NPs resistant <strong>in</strong>dividuals; we recognised two: Atnp01 and Atnp02, resistant to<br />

lethal concentration (for <strong>the</strong> wild type) of NPs. They showed <strong>the</strong> higher photosyn<strong>the</strong>tic and<br />

respiration efficiency <strong>in</strong> <strong>the</strong> presence of <strong>the</strong> contam<strong>in</strong>ant. We determ<strong>in</strong>ed <strong>the</strong> <strong>in</strong>tegrity of <strong>the</strong><br />

<strong>in</strong>serted Ac/Ds transposon, <strong>the</strong> number of transposon copies, and <strong>the</strong>ir positions <strong>with</strong><strong>in</strong> <strong>the</strong><br />

genome of each mutant. We identified two putative <strong>in</strong>sertions for Atnp01 and one for Atnp02.<br />

The next steps were <strong>the</strong> expression analysis of genes visited by <strong>the</strong> Ds element and <strong>the</strong> whole<br />

genome effects on <strong>the</strong> transcription us<strong>in</strong>g Real-Time PCR and Affymetrix microarray<br />

approaches. The relevance of <strong>the</strong> results will be discussed <strong>in</strong> <strong>the</strong> context of develop<strong>in</strong>g a risk<br />

assessment procedure for nanoparticles based on <strong>the</strong> model plant A.thaliana.

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