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Activation-Tagged Suppressors of a Weak Brassinosteroid Receptor Mutant

Authors
Kang, BinWang, HaoNam, Kyoung HeeLi, JiayangLi, Jianming
Issue Date
Jan-2010
Publisher
CELL PRESS
Keywords
Brassinosteroid; BRI1; bri1-301; auxin; YUCCA
Citation
MOLECULAR PLANT, v.3, no.1, pp 260 - 268
Pages
9
Journal Title
MOLECULAR PLANT
Volume
3
Number
1
Start Page
260
End Page
268
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/13296
DOI
10.1093/mp/ssp099
ISSN
1674-2052
1752-9867
Abstract
Brassinosteroids (BRs) are important plant hormones that act synergistically with auxin to regulate a variety of plant developmental and physiological processes. In the past decade, genetic and biochemical studies have revealed a linear signaling pathway that relies on protein phosphorylation to transmit the BR signal into the nucleus, altering expression of hundreds of genes to promote plant growth. We conducted an activation-tagging based suppressor screen to look for Arabidopsis genes that, when overexpressed by inserted 35S enhancer elements, could suppress the dwarf phenotype of a weak BR receptor mutant bri1-301. This screen identified a total of six dominant activation-tagged bri1 suppressors (atbs-Ds). Using a plasmid rescue approach, we discovered that the bri1-301 suppression effect in four atbs-D mutants (atbs3-D to atbs6-D) was caused by overexpression of a YUCCA gene thought to be involved in tryptophan-dependent auxin biosynthesis. Interestingly, the three activation-tagged YUCCA genes belong to the YUCCA IIA subfamily that includes two other members out of 11 known Arabidopsis YUCCA genes. In addition, our molecular studies revealed a T-DNA insertion near a basic helix-loop-helix gene in atbs1-D and a T-DNA insertion in a region carrying a BR biosynthetic gene in atbs2-D. Further studies of these atbs-D mutants could lead to better understanding of the BR signaling process and the BR-auxin interaction.
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