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15th International Conference on Arabidopsis Research - TAIR

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T01-063<br />

C<strong>on</strong>trol of <strong>Arabidopsis</strong> petal size by a novel RING<br />

finger protein<br />

Sabine Disch(1), Jennifer C. Fletcher(2), Michael Lenhard(1)<br />

1-Institut für Biologie III, Universität Freiburg, Schänzlestrasse 1, 79104 Freiburg, Germany<br />

2-USDA/UC Berkeley, Plant Gene Expressi<strong>on</strong> Center, Albany, CA 94710, USA<br />

The species-specific size of plant organs is under tight<br />

genetic c<strong>on</strong>trol as evidenced by the very low variability in<br />

size when genetically identical individuals are grown under<br />

the same envir<strong>on</strong>mental c<strong>on</strong>diti<strong>on</strong>s. However, the genetic and<br />

molecular basis of organ size c<strong>on</strong>trol in plants is largely<br />

unknown.<br />

To begin to dissect the underlying regulatory mechanisms,<br />

we are characterizing a novel <strong>Arabidopsis</strong> mutant, big<br />

brother2 (bb2), that shows a dramatic overgrowth of petals<br />

and to a lesser extent of sepals and the stem. This appears<br />

to be due to an extended period of growth, rather than to<br />

faster growth. The enlargement of petals is independent of<br />

the known growth promoter AINTEGUMENTA (1), suggesting that<br />

bb2 defines a novel regulatory pathway in growth c<strong>on</strong>trol.<br />

The phenotype is due to the deleti<strong>on</strong> of an uncharacterized<br />

gene encoding a protein with a RING-finger domain.<br />

Intriguingly, heterozygous bb2 mutants also show an<br />

intermediate enlargement of organs, suggesting that BB2<br />

regulates organ growth in a dosage-dependent manner.<br />

(1) Mizukami and Fisher (2000), PNAS 97, 942-947<br />

T01 Development 1 (Flower, Fertilizati<strong>on</strong>, Fruit, Seed)<br />

T01-064<br />

Functi<strong>on</strong>al analysis of armadillo repeat-<strong>on</strong>ly (ARO)<br />

proteins in <strong>Arabidopsis</strong> thaliana<br />

M. Gebert(1), T. Dresselhaus(1), S. Sprunck(1)<br />

1-Biocenter Klein Flottbek, Dept. Developmental Biology & Biotechnology, University of Hamburg,<br />

Ohnhorststr.18, D-22609 Hamburg, Germany<br />

The armadillo domain (Arm) was first identified in the Drosophila segment polaritiy<br />

gene armadillo. It codes for beta-catenin, wich functi<strong>on</strong>s in cell to cell<br />

adhesi<strong>on</strong> but also as a comp<strong>on</strong>ent of the wnt-signalling pathway, regulating<br />

cell fate and polarity. Proteins c<strong>on</strong>taining Arm repeats possess tandem copies<br />

of a degenerated protein sequence motif of about 42 amino acids that form a<br />

c<strong>on</strong>served three-dimensi<strong>on</strong>al structure mediating protein-protein interacti<strong>on</strong>s<br />

[1]. Most of these proteins are involved in intracellular signalling or regulati<strong>on</strong><br />

of gene expressi<strong>on</strong> during developmental processes. In c<strong>on</strong>trast to animals,<br />

<strong>on</strong>ly two Arm repeat c<strong>on</strong>taining proteins have been functi<strong>on</strong>ally characterized<br />

in plants [2,3]. Nevertheless, 108 predicted Arm repeat proteins have been<br />

identified in the <strong>Arabidopsis</strong> genome [4], which can be subdivided <strong>on</strong> the<br />

base of their homology and the occurrence of additi<strong>on</strong>al motifs (e.g. U-box,<br />

F-box, S/T kinase, etc). Besides those subfamilies c<strong>on</strong>taining defined motifs<br />

of known functi<strong>on</strong> adjacent to the Arm domain, there is a subgroup of at least<br />

26 Arm genes without any further known protein motif and with yet unknown<br />

functi<strong>on</strong> (ARO). Three of these genes encode proteins with significant homology<br />

to a wheat arm repeat protein from unfertilized egg cells. The wheat<br />

homolog (TaAro1) shows female and male gametophyte-specific expressi<strong>on</strong>.<br />

Likewise, <strong>on</strong>e of the corresp<strong>on</strong>ding A. thaliana genes, AtAro1, can be detected<br />

specifically in female and male gametophytic tissues of <strong>Arabidopsis</strong> by<br />

RT-PCR studies. The other two genes (AtAro2 and AtAro3) are also expressed<br />

in vegetative tissues. Promoter activity of AtAro1 was analyzed using GUS<br />

as a reporter gene. Since database searches revealed the existance of a<br />

putative transmembrane domain for AtAro1, subcellular localizati<strong>on</strong> of the<br />

proteins was investigated using GFP fusi<strong>on</strong> proteins in transient expressi<strong>on</strong><br />

studies. T-DNA inserti<strong>on</strong> lines of all three genes are currently examined for<br />

phenotypes, especially in respect to gametophyte formati<strong>on</strong> and functi<strong>on</strong>.<br />

Future studies include the ectopic overexpressi<strong>on</strong> af AtAro1 and a screening<br />

for interacting proteins.<br />

[1] Coates, J.C. (2003); [2] St<strong>on</strong>e, S.L. et al. (2003); [3] Amador V. et al. (2001) [4] Mudgil, Y. et<br />

al. (2004)<br />

15 th <str<strong>on</strong>g>Internati<strong>on</strong>al</str<strong>on</strong>g> <str<strong>on</strong>g>C<strong>on</strong>ference</str<strong>on</strong>g> <strong>on</strong> <strong>Arabidopsis</strong> <strong>Research</strong> 2004 · Berlin

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