INFIVE   05416
INSTITUTO DE FISIOLOGIA VEGETAL
Unidad Ejecutora - UE
artículos
Título:
Differential regulation of laccase gene expression in Coriolopsis rigida LPSC No. 232
Autor/es:
MARIO CARLOS NAZARENO SAPARRAT; BALATTI, P. A.; MART├ŹNEZ, M. J.; JURADO, M.
Revista:
Fungal Biology
Editorial:
Elsevier Ltd.
Referencias:
Año: 2010 vol. 114 p. 999 - 999
ISSN:
1878-6146
Resumen:
Two laccase isoenzyme genes (lcc2 and lcc3) from the white-rot fungus Coriolopsis rigidawere cloned, and together with the previously described lcc1, their transcript levels wereanalysed by Quantitative RT-PCR in order to study their expression patterns under a rangeof putative inducers (Cu2+, Mn2+, Fe3+, 2,6-dimethoxy-1,4-benzoquinone, H2O2, caffeine,amphotericin B and syringic acid). The highest induction was observed for lcc1 in presenceof copper, and thus, a kinetic study was performed to analyze its effect on temporary lcc1gene expression. Our results showed that upregulation due to copper was linked to growthstage, being highest during the trophophase and decreasing during the idiophase. AmphotericinB increased levels of transcripts of lcc1 and lcc2, syringic acid upregulated lcc1 andlcc3 and 2,6-dimethoxy-1,4-benzoquinone induced lcc2 and lcc3. Possible reasons for whylaccase genes from C. rigida are differentially regulated at the transcriptional level arediscussed.
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