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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-31398

Nair, S K; Wang, N; Turuspekov, Y; Pourkheirandish, M; Sinsuwongwat, S; Chen, G; Sameri, M; Tagiri, A; Honda, I; Watanabe, Y; Kanamori, H; Wicker, T; Stein, N; Nagamura, Y; Matsumoto, T; Komatsuda, T (2010). Cleistogamous flowering in barley arises from the suppression of microRNA-guided HvAP2 mRNA cleavage. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 107(1):490-495.

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The cleistogamous flower sheds its pollen before opening, forcing plants with this habit to be almost entirely autogamous. Cleistogamy also provides a means of escape from cereal head blight infection and minimizes pollen-mediated gene flow. The lodicule in cleistogamous barley is atrophied. We have isolated cleistogamy 1 (Cly1) by positional cloning and show that it encodes a transcription factor containing two AP2 domains and a putative microRNA miR172 targeting site, which is an ortholog of Arabidopsis thaliana AP2. The expression of Cly1 was concentrated within the lodicule primordia. We established a perfect association between a synonymous nucleotide substitution at the miR172 targeting site and cleistogamy. Cleavage of mRNA directed by miR172 was detectable only in a noncleistogamous background. We conclude that the miR172-derived down-regulation of Cly1 promotes the development of the lodicules, thereby ensuring noncleistogamy, although the single nucleotide change at the miR172 targeting site results in the failure of the lodicules to develop properly, producing the cleistogamous phenotype.


57 citations in Web of Science®
57 citations in Scopus®
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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Department of Plant and Microbial Biology
Dewey Decimal Classification:580 Plants (Botany)
Deposited On:18 Feb 2010 20:00
Last Modified:05 Apr 2016 13:57
Publisher:National Academy of Sciences
Additional Information:Copyright: National Academy of Sciences USA
Publisher DOI:10.1073/pnas.0909097107
PubMed ID:20018663

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