Trends in Plant Science
ReviewArabidopsis ovule development and its evolutionary conservation
Section snippets
Molecular control of the determination of ovule identity
Ovules are complex structures that develop from the placenta and are the precursors of seeds. Three fundamental elements can be distinguished from the proximal–distal axis: the funiculus, which attaches the ovule to the placenta; the chalaza, which forms the integument(s); and the nucellus, which is covered by the integuments and in which the megaspore mother cell differentiates to form the embryo sac. Genes that determine the identity of the ovule have been identified and studied in detail in
The control of floral meristem determinacy in relation to placentation types
Various data in the literature support the hypothesis that the mode of placental development determines when floral meristem activity terminates 20, 21, 22, 23. In Petunia and rice, the floral meristem is maintained after carpel primordial development, because placenta and ovules arise directly from the inner part of the floral meristem (Figure 2de). By contrast, in Arabidopsis, both the placenta and the ovules differentiate from the inner ovary wall (Figure 2a–c).
Related to these differences
Upstream and downstream ovule identity genes
Several approaches have been used to identify target genes involved in floral organ identity complexes 30, 31, 32. However, until now, direct target genes of ovule identity factors have not been identified. One promising approach to identify these factors is the use of chromatin immunoprecipitation in combination with massive sequencing approaches, which enables genome-wide identification of target genes [33].
More information is available for upstream regulators of ovule identity genes in
Symmetry establishment during ovule development
Ovules are characterized by a proximal–distal (P–D) symmetry during early stages of development and by an adaxial–abaxial (Ad–Ab) polarity at the time of integument differentiation and elongation. A crucial developmental step is the correct switch from P–D symmetry to Ad–Ab polarity. In Arabidopsis, this switch is marked by initiation of the outer integument on the abaxial side and, from a molecular point of view, by the expression of INO at the abaxial side of the chalaza region, where the
Concluding remarks and future perspectives
We think that an exciting scenario is emerging because, at least for the model species Arabidopsis, a detailed picture of the molecular regulation of ovule development is becoming available. This is accompanied by an increase in our understanding of ovule development in other model species such as rice (Figure 3). Comparing the knowledge that we have obtained from Arabidopsis with the data obtained from other species will allow us to ascertain the extent of conservation of the regulatory
Acknowledgements
We thank Gerco Angenent for providing pictures of the Petunia fbp7;fbp11 co-suppression mutant.
References (61)
Conversion of leaves into petals in Arabidopsis
Curr. Biol.
(2001)The BELL1 gene encodes a homeodomain protein involved in pattern formation in the Arabidopsis ovule primordium
Cell
(1995)Use of Petunia to unravel plant meristem functioning
Trends Plant Sci.
(2005)Termination of stem cell maintenance in Arabidopsis floral meristems by interactions between WUSCHEL and AGAMOUS
Cell
(2001)A molecular link between stem cell regulation and floral patterning in Arabidopsis
Cell
(2001)- et al.
Single-molecule studies of DNA architectural changes induced by regulatory proteins
Methods Enzymol.
(2003) Pattern formation during early ovule development in Arabidopsis thaliana
Dev. Biol.
(2004)Assessing the redundancy of MADS-box genes during carpel and ovule development
Nature
(2003)Genetic and molecular interactions between BELL1 and MADS-box factors support ovule development in Arabidopsis
Plant Cell
(2007)MADS-box protein complexes control ovule and carpel development in Arabidopsis
Plant Cell
(2003)