Genetics, Vol. 162, 1911-1925, December 2002, Copyright © 2002

Embryo and Endosperm Development Is Disrupted in the Female Gametophytic capulet Mutants of Arabidopsis

Paul E. Grinia, Gerd Jürgensa, and Martin Hülskampa
a ZMBP, Developmental Genetics Department, University of Tübingen, D-72076 Tübingen, Germany

Corresponding author: Martin Hülskamp, University of Cologne, Gyrhofstr. 15, D-50931 Cologne, Germany., martin.huelskamp{at}uni-koeln.de (E-mail)

Communicating editor: C. S. GASSER

The female gametophyte of higher plants gives rise, by double fertilization, to the diploid embryo and triploid endosperm, which develop in concert to produce the mature seed. What roles gametophytic maternal factors play in this process is not clear. The female-gametophytic effects on embryo and endosperm development in the Arabidopsis mea, fis, and fie mutants appear to be due to gametic imprinting that can be suppressed by METHYL TRANSFERASE1 antisense (MET1 a/s) transgene expression or by mutation of the DECREASE IN DNA METHYLATION1 (DDM1) gene. Here we describe two novel gametophytic maternal-effect mutants, capulet1 (cap1) and capulet2 (cap2). In the cap1 mutant, both embryo and endosperm development are arrested at early stages. In the cap2 mutant, endosperm development is blocked at very early stages, whereas embryos can develop to the early heart stage. The cap mutant phenotypes were not rescued by wild-type pollen nor by pollen from tetraploid plants. Furthermore, removal of silencing barriers from the paternal genome by MET1 a/s transgene expression or by the ddm1 mutation also failed to restore seed development in the cap mutants. Neither cap1 nor cap2 displayed autonomous seed development, in contrast to mea, fis, and fie mutants. In addition, cap2 was epistatic to fis1 in both autonomous endosperm and sexual development. Finally, both cap1 and cap2 mutant endosperms, like wild-type endosperms, expressed the paternally inactive endosperm-specific FIS2 promoter GUS fusion transgene only when the transgene was introduced via the embryo sac, indicating that imprinting was not affected. Our results suggest that the CAP genes represent novel maternal functions supplied by the female gametophyte that are required for embryo and endosperm development.





This article has been cited by other articles:


Home page
Plant CellHome page
G.-E. Stenvik, N. M. Tandstad, Y. Guo, C.-L. Shi, W. Kristiansen, A. Holmgren, S. E. Clark, R. B. Aalen, and M. A. Butenko
The EPIP Peptide of INFLORESCENCE DEFICIENT IN ABSCISSION Is Sufficient to Induce Abscission in Arabidopsis through the Receptor-Like Kinases HAESA and HAESA-LIKE2
PLANT CELL, July 1, 2008; 20(7): 1805 - 1817.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. Ungru, M. K. Nowack, M. Reymond, R. Shirzadi, M. Kumar, S. Biewers, P. E. Grini, and A. Schnittger
Natural Variation in the Degree of Autonomous Endosperm Formation Reveals Independence and Constraints of Embryo Growth During Seed Development in Arabidopsis thaliana
Genetics, June 1, 2008; 179(2): 829 - 841.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
M. Chen, M. Ha, E. Lackey, J. Wang, and Z. J. Chen
RNAi of met1 Reduces DNA Methylation and Induces Genome-Specific Changes in Gene Expression and Centromeric Small RNA Accumulation in Arabidopsis Allopolyploids
Genetics, April 1, 2008; 178(4): 1845 - 1858.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
Q. A. Ngo, J. M. Moore, R. Baskar, U. Grossniklaus, and V. Sundaresan
Arabidopsis GLAUCE promotes fertilization-independent endosperm development and expression of paternally inherited alleles
Development, November 15, 2007; 134(22): 4107 - 4117.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
M. A. Butenko, G.-E. Stenvik, V. Alm, B. Saether, S. E. Patterson, and R. B. Aalen
Ethylene-dependent and -independent pathways controlling floral abscission are revealed to converge using promoter::reporter gene constructs in the ida abscission mutant
J. Exp. Bot., November 1, 2006; 57(14): 3627 - 3637.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. F. Gutierrez-Marcos, L. M. Costa, and M. M. S. Evans
Maternal Gametophytic baseless1 Is Required for Development of the Central Cell and Early Endosperm Patterning in Maize (Zea mays)
Genetics, September 1, 2006; 174(1): 317 - 329.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
B. Stangeland, R. Nestestog, P. E. Grini, N. Skrbo, A. Berg, Z. Salehian, A. Mandal, and R. B. Aalen
Molecular analysis of Arabidopsis endosperm and embryo promoter trap lines: reporter-gene expression can result from T-DNA insertions in antisense orientation, in introns and in intergenic regions, in addition to sense insertion at the 5' end of genes
J. Exp. Bot., September 1, 2005; 56(419): 2495 - 2505.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
D. Grimanelli, E. Perotti, J. Ramirez, and O. Leblanc
Timing of the Maternal-to-Zygotic Transition during Early Seed Development in Maize
PLANT CELL, April 1, 2005; 17(4): 1061 - 1072.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
G. C. Pagnussat, H.-J. Yu, Q. A. Ngo, S. Rajani, S. Mayalagu, C. S. Johnson, A. Capron, L.-F. Xie, D. Ye, and V. Sundaresan
Genetic and molecular identification of genes required for female gametophyte development and function in Arabidopsis
Development, February 1, 2005; 132(3): 603 - 614.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
A.-M. Sorensen, S. Kroeber, and H. Saedler
The ABNORMAL GAMETOPHYTES (AGM) Gene Product of Arabidopsis Demonstrates a Role in Mitosis During Gamete Development
Plant Cell Physiol., July 15, 2004; 45(7): 905 - 913.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
R. Yadegari and G. N. Drews
Female Gametophyte Development
PLANT CELL, June 1, 2004; 16(suppl_1): S133 - S141.
[Full Text] [PDF]


Home page
Plant CellHome page
J. F. Gutierrez-Marcos, L. M. Costa, C. Biderre-Petit, B. Khbaya, D. M. O'Sullivan, M. Wormald, P. Perez, and H. G. Dickinson
maternally expressed gene1 Is a Novel Maize Endosperm Transfer Cell-Specific Gene with a Maternal Parent-of-Origin Pattern of Expression
PLANT CELL, May 1, 2004; 16(5): 1288 - 1301.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
M. A. Butenko, S. E. Patterson, P. E. Grini, G.-E. Stenvik, S. S. Amundsen, A. Mandal, and R. B. Aalen
INFLORESCENCE DEFICIENT IN ABSCISSION Controls Floral Organ Abscission in Arabidopsis and Identifies a Novel Family of Putative Ligands in Plants
PLANT CELL, October 1, 2003; 15(10): 2296 - 2307.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
M. R. Tucker, A.-C. G. Araujo, N. A. Paech, V. Hecht, E. D. L. Schmidt, J.-B. Rossell, S. C. de Vries, and A. M. G. Koltunow
Sexual and Apomictic Reproduction in Hieracium subgenus Pilosella Are Closely Interrelated Developmental Pathways
PLANT CELL, July 1, 2003; 15(7): 1524 - 1537.
[Abstract] [Full Text] [PDF]