4.6 Article

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

期刊

NEW PHYTOLOGIST
卷 198, 期 2, 页码 398-407

出版社

WILEY-BLACKWELL
DOI: 10.1111/nph.12160

关键词

comparative genomics; light harvesting complex; Macrocystis pyrifera (giant kelp); Phaeophyceae; quantitative PCR; RNA-Seq; transcriptomics; water-column gradients

资金

  1. National Science Foundation
  2. Mia J. Tegner Fellowship
  3. Sigma Xi Grant-in-Aid of Research
  4. Beyster Foundation
  5. [NSF-OCE-1136477]
  6. [NSF-MCB-1024913]
  7. [DOE-DE-SC0006719]
  8. Direct For Biological Sciences
  9. Div Of Biological Infrastructure [1103652] Funding Source: National Science Foundation

向作者/读者索取更多资源

To increase knowledge of transcript diversity for the giant kelp, Macrocystis 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 18m 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 228Mbp of sequence generated c. 9000 isotigs and c. 12000 open reading frames. Annotations were assigned using families of hidden Markov models for c. 11% of open reading frames; M.pyrifera had highest similarity to other members of the Phaeophyceae, namely Ectocarpus siliculosus and Laminaria 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 LI818 (also known as LHCSR) family, showed high expression in the surface compared with 18m 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.

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