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15th International Conference on Arabidopsis Research - TAIR

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T02-067<br />

TYPE-B RESPONSE REGULATORS FUNCTIONALLY<br />

OVERLAP IN THE REGULATION OF CYTOKININ<br />

RESPONSES<br />

Michael Mas<strong>on</strong>(1), Dennis Matthews(2), Eric Schaller(1)<br />

1-Biological Sciences Dept. Dartmouth College, NH. USA.<br />

2-Plant Biology Dept. University of New Hampshire, NH. USA.<br />

Two-comp<strong>on</strong>ent signaling systems involve histidine kinases, histidinec<strong>on</strong>taining<br />

phosphotransfer proteins, and resp<strong>on</strong>se regulators, and have<br />

been implicated in plant resp<strong>on</strong>ses to horm<strong>on</strong>es and envir<strong>on</strong>mental factors.<br />

Genomic analysis of <strong>Arabidopsis</strong> thaliana supports the existence of 22 resp<strong>on</strong>se<br />

regulators (ARRs) that can be divided into at least two distinct groups<br />

designated type-A and type-B. Phylogenetic analysis indicates that the type-B<br />

family is composed of <strong>on</strong>e major and two minor subfamilies. The expressi<strong>on</strong><br />

of the type-B ARRs was examined by using both RT-PCR and GUS fusi<strong>on</strong><br />

c<strong>on</strong>structs. The major subfamily of type-B ARRs showed particularly high<br />

expressi<strong>on</strong> in regi<strong>on</strong>s where cytokinins play a major role, including cells near<br />

the apical meristem and in young leaves that would be undergoing cell divisi<strong>on</strong>.<br />

Type-B ARRs were also found near the root tip with highest expressi<strong>on</strong> in<br />

the root el<strong>on</strong>gati<strong>on</strong> z<strong>on</strong>e. Based up<strong>on</strong> the analysis of T-DNA inserti<strong>on</strong> mutant<br />

lines, we found that the members of the major subfamily of type-B ARRs not<br />

<strong>on</strong>ly show similarities in expressi<strong>on</strong> but also appear to functi<strong>on</strong>ally overlap. Of<br />

the single mutants, <strong>on</strong>ly arr1 plants displayed clearly reduced cytokinin sensitivity.<br />

Progressively greater insensitivity to cytokinin was observed in higher<br />

order mutants. Our data support a role for multiple type-B ARRs in modulating<br />

cytokinin resp<strong>on</strong>ses with ARR1 playing the most significant role.<br />

T02 Development 2 (Shoot, Root)<br />

T02-068<br />

Analysis of TRANSPARENT TESTA GLABRA2 involved<br />

in trichome differentiati<strong>on</strong><br />

Tetsuya Ishida(1), Sayoko Hattori(1), Kiyotaka Okada(1, 2), Takuji Wada(1)<br />

1-Plant Science Center, RIKEN<br />

2-Graduate School of Science, Kyoto University<br />

Trichomes and root hairs are specialized cells differentiated from the<br />

epidermis. Several genes have been identified as regulators of epidermal<br />

cell differentiati<strong>on</strong>, playing a role in the development of these special cells.<br />

The <strong>Arabidopsis</strong> TRANSPARENT TESTA GLABRA2 (TTG2) gene encodes a<br />

WRKY transcripti<strong>on</strong> factor. The ttg2 mutant has fewer trichomes than the<br />

wild type, its trichomes are less branched, and it has defects in tannin and<br />

mucilage producti<strong>on</strong> in its seed coat. TTG2 is expressed in leaf primordia,<br />

trichomes, seed coats, and hairless cells of developing roots. It is proposed<br />

that TTG2 functi<strong>on</strong>s downstream of TRANSPARENT TESTA GLABRA1 (TTG1)<br />

and GLABRA1 (GL1), and shares functi<strong>on</strong>s with GLABRA2 (GL2) in trichome<br />

development (Johns<strong>on</strong> et al., 2002).<br />

To further elucidate the relati<strong>on</strong>ship between TTG2 and other genes that<br />

regulate epidermis differentiati<strong>on</strong>, we analyzed TTG2 expressi<strong>on</strong> in various<br />

trichome and root hair mutants. We found that TTG2 expressi<strong>on</strong> in roots was<br />

suppressed in the werewolf-1 (wer-1) mutant, and that TTG2 is ectopically<br />

expressed in root-hair cells in the caprice-1 (cpc-1) mutant. These results<br />

suggest that TTG2 is positively regulated by WER and negatively regulated<br />

by CPC. WER encodes a MYB protein homologous to GL1, and negatively<br />

regulates root-hair cell differentiati<strong>on</strong>. CPC encodes a small MYB protein and<br />

promotes root-hair cell differentiati<strong>on</strong>. There are several putative Myb binding<br />

sites in the TTG2 promoter. We are analyzing transgenic plants carrying a<br />

deleti<strong>on</strong> series of TTG2 promoter::GUS to determine whether or not Myb<br />

proteins directly regulate TTG2.<br />

We also analyzed phenotypes of double mutants of ttg2-1 which had<br />

some trichome mutati<strong>on</strong>s. In the glabra3-2 (gl3-2) mutant, the number of<br />

trichomes is reduced, and its trichomes are less branched than those of the<br />

wild type. In the ttg2-1 gl3-2 double mutant, the number of trichomes was<br />

much reduced, and trichomes were detected as small pointed outgrowths.<br />

In the triptych<strong>on</strong>-82 (try-82) mutant, trichomes are often clustered and more<br />

branched than those of the wild type. In the ttg2-1 try-82 double mutant,<br />

the number of trichomes was intermediate between those of its parental<br />

mutants, and its trichomes were similar to those of the ttg2-1 mutant. We will<br />

discuss the genetic interacti<strong>on</strong> of TTG2 with other regulators of epidermal cell<br />

differentiati<strong>on</strong>.<br />

Johns<strong>on</strong>, C. S. et al. (2002) Plant Cell 14: 1359-1375<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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