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[sgn.git] / cgi-bin / community / feature / 200408.pl
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1 use strict;
2 use CXGN::Page;
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4 my $stylesheet=<<END_STYLESHEET;
5 <style type="text/css">
6 <!--
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12 p {
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30 $page->header('The Unit of Plant Biology', undef, $stylesheet);
31 print<<END_HEREDOC;
33 <center>
34 <h1>The Unit of Plant Biology - Louvain-la-Neuve</h1>
35 </center>
37 <h2>Research Focus</h2>
39 <p>The research interests of the Unit of Plant Biology are
40 focused on two main topics: i) investigating a key developmental
41 change in plant life cycle, namely flowering (J.-M. Kinet), ii)
42 understanding the physiological, genetic and biochemical basis of
43 sensing and responding to environmental cues such as drought,
44 cold, mineral toxicity and other abiotic signals by which plants
45 interact with their surroundings (H. Batoko and S. Lutts). A
46 comprehensive set of approaches are currently used including
47 whole plant physiology (S. Lutts and J.M. Kinet), biochemistry
48 (S. Lutts), histology (J.-M. Kinet), cell and molecular biology
49 (H. Batoko). A variety of plant species are investigated
50 (Arabidopsis thaliana, rice, xero-halophyte species belonging to
51 the genus Atriplex, Fagopyrum esculentum, etc.), the choices
52 being driven mostly by conceptual or specific hypotheses-based
53 suitability.</p>
55 <p>Tomato is among the main model-plants used in the laboratory.
56 The main objectives of the ongoing researchs are:</p>
58 <ol>
59 <li><p>to study the salt tolerance mechanisms in Lycopersicon
60 esculentum and its wild relatives (namely L. chesmanii and L.
61 pennellii) in relation to the role of the SOS pathway in ion
62 homeostasis (Fig. 1)</p>
64 <center>
65 <img src="/static_content/community/feature/200408-1.png" border="0" width="435" height="275"
66 alt="Figure 1" /><br />
67 Figure 1. Zhu, J.-K., 2003<br />
68 Curr.Op. Plant. Biol., 6, 441-445
69 </center>
70 </li>
72 <li><p>to characterize the impact of Cd in relation to oxidative
73 stress and phytochelatine synthesis.</p></li>
75 <li><p>to characterize genes involved in flowering. Up to now, the
76 main focus was on uf mutant which initiates single flowers
77 instead of multi- flowered inflorescences (Fig. 2). Ongoing
78 work has already established that UNIFLORA is a pivotal gene
79 that regulates floral transition and the identity of the
80 inflorescential meristem in tomato. Other mutations that are
81 concomitantly investigated include compound inflorescence,
82 jointless, blind, single flower truss and self pruning.</p></li>
83 </ol>
85 <center>
86 <img src="/static_content/community/feature/200408-2.jpg" border="0" width="450" height="660"
87 alt="solitary, normal and fertile flowers" /> <img src=
88 "/static_content/community/feature/200408-3.jpg" border="0" width="414" height="660" alt=
89 "SEM views" /><br />
90 Figure 2. The reproductive structure of the uf tomato mutant.
91 Left: solitary, normal and fertile flowers are consistently
92 produced instead of inflorescences. Right: SEM views of a same
93 uf-induced floral structure showing that the single-flower
94 phenotype results from the inability of the plant to produce an
95 inflorescence and not from post-initiation abortion processes
96 affecting young flower buds. The isolated flower is seen with
97 its 6 sepals (1 to 6) and was initiated after the formation of
98 the 12th leaf (A). An axillary bud (AB) bearing three leaves
99 (B,C, D) has been initiated at the basis of the flower (Dielen,
100 et al., 1998. Plant Growth Regul., <strong>25</strong>,
101 149-157).
102 </center>
104 <h2>Some Publications</h2>
106 <div style="margin-left: 40px">
107 <p class="bibliography">Bajji, M., Kinet, J.M. and Lutts, S.
108 1998. Salt stress effects on roots and leaves of Atriplex
109 halimus L. and their corresponding callus cultures. Plant Sci.,
110 137, 131-142.</p>
112 <p class="bibliography">Lutts, S., Majerus, V. and Kinet, J.M.
113 1999. NaCl effects on proline metabolism in rice (Oryza sativa
114 ) seedlings. Physiol. Plant., 105, 450- 458.</p>
116 <p class="bibliography">Batoko, H., Zheng, H.-Q., Hawes, C. and
117 Moore, I. 2000. A Rab1 GTPase is required for transport between
118 the endoplasmic reticulum and Golgi apparatus and for normal
119 Golgi movement in plants. Plant Cell, 12, 2201-2217</p>
121 <p class="bibliography">Dielen, V., Lecouvet, V., Dupont, S.
122 and Kinet, J.M. 2001. In vitro control of floral transition in
123 tomato (Lycopersicon esculentum Mill.), the model for
124 autonomously flowering plants, using the late flowering
125 uniflora mutant. J. Exp. Bot., 52, 715-723.</p>
127 <p class="bibliography">Geelen, D., Leyman, B., Batoko, H., Di
128 Sansebastiano, G.-P., Moore, I. and Blatt, M.R. 2002. The
129 abscissic acid-related SNARE homolog NtSyr1 contributes to
130 secretion and growth: evidence from competition with its
131 cytosolic domain Plant Cell, 14, 387-406.</p>
133 <p class="bibliography">Martinez, J.P., Ledent, J.F., Bajji,
134 M., Kinet, J.M. and Lutts, S. 2003. Effect of water stress on
135 growth, Na+ and K+ accumulation and water use efficiency in
136 relation to osmotic adjustment in two populations of Atriplex
137 halimus L. Plant Growth Regul., 41, 63-73.</p>
139 <p class="bibliography">Dielen, V., Quinet, M., Chao, J.,
140 Batoko, H., Havelange, A. and Kinet, J.M. 2004. UNIFLORA, a
141 pivotal gene that regulates floral transition and meristem
142 identity in tomato (Lycopersicon esculentum Mill.). New
143 Phytol., 161, 393-400.</p>
145 <p class="bibliography">Quinet, M., Cawoy, V., Lef\350vre, I.,
146 Van Miegroet, F., Jacquemart, A.L. and Kinet, J.M. 2004.
147 Inflorescence structure and control of flowering time and
148 duration by light in buckwheat (Fagopyrum esculentum Moench.).
149 J. Exp. Bot., 55, 1509-1517.</p>
151 <p class="bibliography">Lutts, S., Lef\350vre, I.,
152 Delp&eacute;r&eacute;e, C., Kivits, S., Dechamps, C., Robledo,
153 A. and Correal, E. 2004. Heavy metal accumulation by the
154 halophyte species Atriplex halimus, a promising species for
155 phytoremediation purposes. J. Environm. Qual., 33, in
156 press.</p>
157 </div>
159 <h2>Contact</h2>
161 <p>Jean-Marie Kinet - Stanley Lutts - Henri Batoko<br />
162 Universit&eacute; catholique de Louvain<br />
163 Unit&eacute; de Biologie v&eacute;g&eacute;tale<br />
164 D&eacute;partement de Biologie et Institut des Sciences de la Vie
165 (ISV)<br />
166 Croix du Sud, 5 (bte 13)<br />
167 B-1348 Louvain-la-Neuve<br />
168 Belgium<br />
169 Fax : +32 10 47 34 35<br />
170 <br />
171 JMK : Tel : +32 10 47 20 50 - Email : <a href=
172 "mailto:kinet\@bota.ucl.ac.be">kinet\@bota.ucl.ac.be</a><br />
173 SL : Tel : +32 10 47 20 37 - Email : <a href=
174 "mailto:lutts\@bota.ucl.ac.be">lutts\@bota.ucl.ac.be</a><br />
175 HB : Tel : +32 10 47 92 65 - Email : <a href=
176 "mailto:batoko\@bota.ucl.ac.be">batoko\@bota.ucl.ac.be</a><br />
177 <br />
178 For more information, please visit the lab's website at<br />
179 <a href=
180 "http://www.bota.ucl.ac.be/Acces.html">http://www.bota.ucl.ac.be/Acces.html</a><br />
182 <br />
183 (note that an english version of the site will be launched
184 soon).</p>
185 END_HEREDOC
186 $page->footer();