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Transcriptomic analysis of metabolic function in the giant kelp, M acrocystis pyrifera , across depth and season

To increase knowledge of transcript diversity for the giant kelp, M acrocystis pyrifera , and assess gene expression across naturally occurring depth gradients in light, temperature and nutrients, we sequenced four cDNA libraries created from blades collected at the sea surface and at 18 m depth dur...

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Bibliographic Details
Published in:The New phytologist 2013-04, Vol.198 (2), p.398-407
Main Authors: Konotchick, Talina, Dupont, Christopher L., Valas, Ruben E., Badger, Jonathan H., Allen, Andrew E.
Format: Article
Language:English
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Summary:To increase knowledge of transcript diversity for the giant kelp, M acrocystis pyrifera , and assess gene expression across naturally occurring depth gradients in light, temperature and nutrients, we sequenced four cDNA libraries created from blades collected at the sea surface and at 18 m depth during the winter and summer. Comparative genomics cluster analyses revealed novel gene families (clusters) in existing brown alga expressed sequence tag data compared with other related algal groups, a pattern also seen with the addition of M . pyrifera sequences. Assembly of 228 Mbp of sequence generated c . 9000 isotigs and c . 12 000 open reading frames. Annotations were assigned using families of hidden M arkov models for c . 11% of open reading frames; M . pyrifera had highest similarity to other members of the P haeophyceae, namely E ctocarpus siliculosus and L aminaria digitata . Quantitative polymerase chain reaction of transcript targets verified depth‐related differences in gene expression; stress response and light‐harvesting transcripts, especially members of the LI 818 (also known as LHCSR ) family, showed high expression in the surface compared with 18 m depth, while some nitrogen acquisition transcripts (e.g. nitrite reductase) were upregulated at depth compared with the surface, supporting a conceptual biological model of depth‐dependent physiology.
ISSN:0028-646X
1469-8137
DOI:10.1111/nph.12160