A1 Refereed original research article in a scientific journal

Transcription and redox enzyme activities: comparison of equilibrium and disequilibrium levels in the three-spined stickleback




AuthorsNikinmaa M, McCairns RJS, Nikinmaa MW, Vuori KA, Kanerva M, Leinonen T, Primmer CR, Merila J, Leder EH

PublisherROYAL SOC

Publication year2013

JournalProceedings of the Royal Society B: Biological Sciences

Journal name in sourcePROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES

Journal acronymP ROY SOC B-BIOL SCI

Article number20122974

Number in series1755

Volume280

Issue1755

Number of pages9

ISSN0962-8452

DOIhttps://doi.org/10.1098/rspb.2012.2974


Abstract
Evolutionary and acclimatory responses require functional variability, but in contrast with mRNA and protein abundance data, most physiological measurements cannot be obtained in a high-throughput manner. Consequently, one must either rely on high-throughput transcriptomic or proteomic data with only predicted functional information, or accept the limitation that most physiological measurements can give fewer data than those provided by transcriptomics or proteomics. We evaluated how transcriptional and redox enzyme activity data agreed with regard to population differentiation (i.e. a system in steady state in which any time lag between transcription, translation and post-translational effects would be irrelevant) and in response to an acute 6 degrees C increase in temperature (i.e. a disequilibrium state wherein translation could not have caught up with transcription) in the three-spined stickleback (Gasterosteus aculeatus). Transcriptional and enzyme activity data corresponded well with regard to population differentiation, but less so with regard to acute temperature increase. The data thus suggest that transcriptional and functional measurements can lead to similar conclusions when a biological system is in a steady state. The responses to acute changes must, as has been demonstrated earlier, be based on changes in cellular conditions or properties of existing proteins without significant de novo synthesis of new gene products.



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