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Six-rowed barley originated from a mutation in a homeodomain-leucine zipper I-class homeobox gene.

Authors :
Komatsuda, Takao
Pourkheirandish, Mohammad
Congfen He
Azhaguvel, Perumal
Kanamori, Hiroyuki
Perovic, Dragan
Stein, Nils
Graner, Andreas
Wicker, Thomas
Tagiri, Akemi
Lundqvist, Udda
Fujimura, Tatsuhito
Matsuoka, Makoto
Matsumoto, Takashi
Yano, Masahiro
Source :
Proceedings of the National Academy of Sciences of the United States of America. 1/23/2007, Vol. 104 Issue 4, p1424-1429. 6p. 4 Graphs.
Publication Year :
2007

Abstract

Increased seed production has been a common goal during the domestication of cereal crops, and early cultivators of barley (Hordeum vulgare ssp. vu!gare) selected a phenotype with a six-rowed spike that stably produced three times the usual grain number. This improved yield established barley as a founder crop for the Near Eastern Neolithic civilization. The barley spike has one central and two lateral spikelets at each rachis node. The wild-type progenitor (H. vulgare ssp. spontaneum) has a two-rowed phenotype, with additional, strictly rudimentary, lateral rows; this natural adaptation is advantageous for seed dispersal after shattering. Until recently, the origin of the six-rowed phenotype remained unknown. In the present study, we isolated vrs1 (six-rowed spike 1), the gene responsible for the six-rowed spike in barley, by means of positional cloning. The wild-type Vrs1 allele (for two-rowed barley) encodes a transcription factor that includes a homeodomain with a closely linked leucine zipper motif. Expression of Vrs1 was strictly localized in the lateral-spikelet primordia of immature spikes, suggesting that the VRS1 protein suppresses development of the lateral rows. Loss of function of Vrs1 resulted in complete conversion of the rudimentary lateral spikelets in two-rowed barley into fully developed fertile spikelets in the six-rowed phenotype. Phylogenetic analysis demonstrated that the six-rowed phenotype originated repeatedly, at different times and in different regions, through independent mutations of Vrs1. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
104
Issue :
4
Database :
Academic Search Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
23960518
Full Text :
https://doi.org/10.1073/pnas.0608580104