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15th International Conference on Arabidopsis Research - TAIR

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T01-091<br />

Functi<strong>on</strong>al analysis of a phosphatidic acid in ABA<br />

signaling during germinati<strong>on</strong><br />

Takeshi Katagiri(1), Masatomo Kabayashi(2), Kazuo Shinozaki(1)<br />

1-Plant Molecular Biology Laboratory, RIKEN Tsukuba Institute<br />

2-Experimental Plant Divisi<strong>on</strong>, RIKEN Bioresouce Center<br />

The horm<strong>on</strong>e abscisic acid (ABA) regulates developmental processes and<br />

stress resp<strong>on</strong>ses in plants. In this study we analyzed a role of a phosphatidic<br />

acid (PA) in ABA signal transducti<strong>on</strong> during seed germinati<strong>on</strong>. A physiological<br />

analysis showed PA triggers early signal transducti<strong>on</strong> events that lead to the<br />

ABA resp<strong>on</strong>ses during seed germinati<strong>on</strong>.<br />

To examine the possible functi<strong>on</strong> of PA during germinati<strong>on</strong>, we measured<br />

PA producti<strong>on</strong>, and found that PA increased. Phosphatidic acid phosphatase<br />

(PAP) is an enzyme that catalyzes PA to diacylglycerol. We analyzed a role of<br />

PAP in PA signaling during germinati<strong>on</strong>. There are four genes for <strong>Arabidopsis</strong><br />

genome. To identify functi<strong>on</strong>al PAP genes during germinati<strong>on</strong> process, we<br />

analyzed expressi<strong>on</strong> of the four PAP genes and phenotypes of their knockout<br />

mutants. The PAP-knockout plant revealed a hypersensitive phenotype to<br />

ABA and accumulated PA during germinati<strong>on</strong>. These results suggest that PAP<br />

is involved in ABA signaling during seed germinati<strong>on</strong>.<br />

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

T01-092<br />

Analysis of sepal and petal development using fl51<br />

mutant of <strong>Arabidopsis</strong><br />

Noriyoshi Yagi(1), Seiji Takeda(1), Ryuji Tsugeki(1), Kiyotaka Okada(1, 2)<br />

1-Department of Botany, Graduate School of Science, Kyoto University<br />

2-CREST, Japan Science and Technology Agency<br />

<strong>Arabidopsis</strong> flowers are composed of four types of floral organs, four sepals,<br />

four petals, six stamens, and two fused carpels. Each type of organ forms in<br />

a c<strong>on</strong>centric whorl. It is well known that the organ identity is established in<br />

c<strong>on</strong>centric pattern by floral homeotic genes. On the other hand, floral organ<br />

positi<strong>on</strong> is defined in each whorl in relati<strong>on</strong> to a putative axis in the floral<br />

meristem, indicating regulatory mechanisms c<strong>on</strong>trolling the positi<strong>on</strong> of floral<br />

organ within each whorl. For proper development of floral organs, primordia<br />

formati<strong>on</strong> and growth such as differentiati<strong>on</strong> and proliferati<strong>on</strong> of cells are to<br />

be strictly c<strong>on</strong>trolled. However, these developmental processes are not well<br />

understood. To identify the genes and mechanisms c<strong>on</strong>trolling primordia<br />

formati<strong>on</strong> and growth, we are analyzing fl51 mutant showing defects in sepal<br />

and petal development.<br />

In fl51, four sepals and petals are narrower and l<strong>on</strong>ger than those of wild<br />

type, though their identities are normal. Sepals are sometimes fused al<strong>on</strong>g<br />

their edges towards the base. Lateral sepal primordia are smaller than those<br />

of wild type, and their positi<strong>on</strong> shifted toward either the abaxial or adaxial<br />

sepal primordium. By positi<strong>on</strong>al cl<strong>on</strong>ing, we found that FL51 gene encoded<br />

a protein that was a comp<strong>on</strong>ent of the spliceosome. This suggests that FL51<br />

protein is required for mRNA splicing of genes involved in the formati<strong>on</strong> and<br />

growth of primordia of sepals and petals. An RT-PCR assay revealed that<br />

FL51 gene was expressed in almost all tissue, though the abnormalities in<br />

fl51 are c<strong>on</strong>fined to sepals and petals. In fl51, a nucleotide change occurred<br />

at the splice d<strong>on</strong>or site, resulting in miss splicing. From database search, in<br />

additi<strong>on</strong> to FL51 gene, <strong>on</strong>e FL51-related gene was found in <strong>Arabidopsis</strong>.<br />

We are examining the spatial and temporal expressi<strong>on</strong> patterns of FL51<br />

gene in inflorescences by mRNA in situ hybridizati<strong>on</strong>. We are also analyzing<br />

the phenotype of T-DNA inserti<strong>on</strong> lines of FL51 to investigate differences in<br />

the effect to floral organ development between severe alleles with weak <strong>on</strong>es<br />

of fl51 mutants. In additi<strong>on</strong>, we investigate the relati<strong>on</strong>ship between FL51<br />

gene and other floral genes by using double mutants. The phenotype of fl51,<br />

expressi<strong>on</strong> and functi<strong>on</strong> of FL51 will be presented.<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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