ATP-Binding Cassette Transporter G26 Is Required for Male Fertility and Pollen Exine Formation in Arabidopsis
The highly resistant biopolymer, sporopollenin, gives the outer wall (exine) of spores and pollen grains their unparalleled strength, shielding these structures from terrestrial stresses. Despite a limited understanding of the composition of sporopollenin, it appears that the synthesis of sporopolle...
Saved in:
Published in | Plant physiology (Bethesda) Vol. 154; no. 2; pp. 678 - 690 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Rockville, MD
American Society of Plant Biologists
01.10.2010
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | The highly resistant biopolymer, sporopollenin, gives the outer wall (exine) of spores and pollen grains their unparalleled strength, shielding these structures from terrestrial stresses. Despite a limited understanding of the composition of sporopollenin, it appears that the synthesis of sporopollenin occurs in the tapetum and requires the transport of one or more sporopollenin constituents to the surface of developing microspores. Here, we describe ABCG26, a member of the ATP-binding cassette (ABC) transporter superfamily, which is required for pollen exine formation in Arabidopsis (Arabidopsis thaliana). abcg26 mutants are severely reduced in fertility, with most siliques failing to produce seeds by self-fertilization and mature anthers failing to release pollen. Transmission electron microscopy analyses revealed an absence of an exine wall on abcg26-1 mutant microspores. Phenotypic abnormalities in pollen wall formation were first apparent in early uninucleate microspores as a lack of exine formation and sporopollenin deposition. Additionally, the highest levels of ABCG26 mRNA were in the tapetum, during early pollen wall formation, sporopollenin biosynthesis, and sporopollenin deposition. Accumulations resembling the trilamellar lipidic coils in the abcg11 and abcg12 mutants defective in cuticular wax export were observed in the anther locules of abcg26 mutants. A yellow fluorescent protein-ABCG26 protein was localized to the endoplasmic reticulum and plasma membrane. Our results show that ABCG26 plays a critical role in exine formation and pollen development and are consistent with a model by which ABCG26 transports sporopollenin precursors across the tapetum plasma membrane into the locule for polymerization on developing microspore walls. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The online version of this article contains Web-only data. www.plantphysiol.org/cgi/doi/10.1104/pp.110.161968 The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Carl J. Douglas (cdouglas@interchange.ubc.ca). This work was supported by Discovery Grants from the Natural Sciences and Engineering Research Council of Canada (NSERC) to C.J.D. and A.L.S., by an NSERC Graduate Fellowship to T.D.Q., and by the NSERC CREATE training grant Working on Walls. Open Access articles can be viewed online without a subscription. |
ISSN: | 0032-0889 1532-2548 1532-2548 |
DOI: | 10.1104/pp.110.161968 |