Role of callose synthases in transfer cell wall development in tocopherol deficient Arabidopsis mutants

被引:32
|
作者
Maeda, Hiroshi [1 ,2 ,3 ]
Song, Wan [1 ,4 ]
Sage, Tammy [5 ]
DellaPenna, Dean [1 ]
机构
[1] Michigan State Univ, Dept Biochem & Mol Biol, E Lansing, MI 48824 USA
[2] Michigan State Univ, Cell & Mol Biol Program, E Lansing, MI 48824 USA
[3] Univ Wisconsin, Dept Bot, Madison, WI USA
[4] Michigan State Univ, Genet Program, E Lansing, MI 48824 USA
[5] Univ Toronto, Dept Ecol & Evolutionary Biol, Toronto, ON, Canada
来源
FRONTIERS IN PLANT SCIENCE | 2014年 / 5卷
基金
加拿大自然科学与工程研究理事会;
关键词
tocopherols; transfer cells; callose synthase; Arabidopsis; sugar export; antioxidants; phloem parenchyma cells; DIFFERENTIAL GENE-EXPRESSION; SYNECHOCYSTIS SP PCC-6803; ALPHA-TOCOPHEROL; VITAMIN-E; HOMOGENTISATE PHYTYLTRANSFERASE; LIPID-PEROXIDATION; DESATURASE; RAT; STRESS; EXPORT;
D O I
10.3389/fpls.2014.00046
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Tocopherols (vitamin E) are lipid-soluble antioxidants produced by all plants and algae, and many cyanobacteria, yet their functions in these photosynthetic organisms are still not fully understood. We have previously reported that the vitamin E deficient 2 (vte2) mutant of Arabidopsis thaliana is sensitive to low temperature (LT) due to impaired transfer cell wall (TCW) development and photoassimilate export associated with massive callose deposition in transfer cells of the phloem. To further understand the roles of tocopherols in LT induced TCW development we compared the global transcript profiles of vte2 and wild-type leaves during LT treatment. Tocopherol deficiency had no significant impact on global gene expression in permissive conditions, but significantly affected expression of 77 genes after 48 h of LT treatment. In vte2 relative to wild type, genes associated with solute transport were repressed, while those involved in various pathogen responses and cell wall modifications, including two members of callose synthase gene family, GLUCAN SYNTHASE LIKE 4 (GSL4) and GSL11, were induced. However, introduction of gsl4 or gsl11 mutations individually into the vte2 background did not suppress callose deposition or the overall LT-induced phenotypes of vte2. Intriguingly, introduction of a mutation disrupting GSL5, the major GSL responsible for pathogen-induced callose deposition, into vte2 substantially reduced vascular callose deposition at LT, but again had no effect on the photoassimilate export phenotype of LT-treated vte2. These results suggest that GSL5 plays a major role in TCW callose deposition in LT-treated vte2 but that this GSL5-dependent callose deposition is not the primary cause of the impaired photoassimilate export phenotype.
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页数:15
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