Differential gene expression in senescing leaves of two silver birch genotypes in response to elevated CO 2 and tropospheric ozone

ABSTRACT Long‐term effects of elevated CO 2 and O 3 concentrations on gene expression in silver birch ( Betula pendula Roth) leaves were studied during the end of the growing season. Two birch genotypes, clones 4 and 80, with different ozone growth responses, were exposed to 2× ambient CO 2 and/or O...

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Published inPlant, cell and environment Vol. 33; no. 6; pp. 1016 - 1028
Main Authors KONTUNEN‐SOPPELA, SARI, RIIKONEN, JOHANNA, RUHANEN, HANNA, BROSCHÉ, MIKAEL, SOMERVUO, PANU, PELTONEN, PETRI, KANGASJÄRVI, JAAKKO, AUVINEN, PETRI, PAULIN, LARS, KEINÄNEN, MARKKU, OKSANEN, ELINA, VAPAAVUORI, ELINA
Format Journal Article
LanguageEnglish
Published 01.06.2010
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Summary:ABSTRACT Long‐term effects of elevated CO 2 and O 3 concentrations on gene expression in silver birch ( Betula pendula Roth) leaves were studied during the end of the growing season. Two birch genotypes, clones 4 and 80, with different ozone growth responses, were exposed to 2× ambient CO 2 and/or O 3 in open‐top chambers (OTCs). Microarray analyses were performed after 2 years of exposure, and the transcriptional profiles were compared to key physiological characteristics during leaf senescence. There were genotypic differences in the responses to CO 2 and O 3 . Clone 80 exhibited greater transcriptional response and capacity to alter metabolism, resulting in better stress tolerance. The gene expression patterns of birch leaves indicated contrasting responses of senescence‐related genes to elevated CO 2 and O 3 . Elevated CO 2 delayed leaf senescence and reduced associated transcriptional changes, whereas elevated O 3 advanced leaf senescence because of increased oxidative stress. The combined treatment demonstrated that elevated CO 2 only temporarily alleviated the negative effects of O 3 . Gene expression data alone were insufficient to explain the O 3 response in birch, and additional physiological and biochemical data were required to understand the true O 3 sensitivity of these clones.
ISSN:0140-7791
1365-3040
DOI:10.1111/j.1365-3040.2010.02123.x