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Luo, Y., Dong, X., Yu, T., Shi, X., Li, Z., Yang, W., . . . Karrenberg, S. (2015). A Single Nucleotide Deletion in Gibberellin20-oxidase1 Causes Alpine Dwarfism in Arabidopsis. Plant Physiology, 168(3), 930-937
Open this publication in new window or tab >>A Single Nucleotide Deletion in Gibberellin20-oxidase1 Causes Alpine Dwarfism in Arabidopsis
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2015 (English)In: Plant Physiology, ISSN 0032-0889, E-ISSN 1532-2548, Vol. 168, no 3, p. 930-937Article in journal (Refereed) Published
Abstract [en]

Alpine dwarfism is widely observed in alpine plant populations and often considered a high-altitude adaptation, yet its molecular basis and ecological relevance remain unclear. In this study, we used map-based cloning and field transplant experiments to investigate dwarfism in natural Arabidopsis (Arabidopsis thaliana) accessions collected from the Swiss Alps. A loss-of-function mutation due to a single nucleotide deletion in gibberellin20-oxidase1 (GA5) was identified as the cause of dwarfism in an alpine accession. The mutated allele, ga5-184, was found in two natural Arabidopsis populations collected from one geographic region at high altitude, but was different from all other reported ga5 null alleles, suggesting that this allele has evolved locally. In field transplant experiments, the dwarf accession with ga5-184 exhibited a fitness pattern consistent with adaptation to high altitude. Across a wider array of accessions from the Swiss Alps, plant height decreased with altitude of origin, but fitness patterns in the transplant experiments were variable and general altitudinal adaptation was not evident. In general, our study provides new insights into molecular basis and possible ecological roles of alpine dwarfism, and demonstrates the importance of the GA-signaling pathway for the generation of ecologically relevant variation in higher plants.

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Biological Sciences
Identifiers
urn:nbn:se:uu:diva-262000 (URN)10.1104/pp.15.00005 (DOI)000359307600016 ()25941313 (PubMedID)
Available from: 2015-09-07 Created: 2015-09-07 Last updated: 2017-12-04Bibliographically approved
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0001-8253-5137

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