An Arabidopsis callose synthase, GSL5, is required for wound and papillary callose formation

被引:382
作者
Jacobs, AK
Lipka, V
Burton, RA
Panstruga, R
Strizhov, N
Schulze-Lefert, P [1 ]
Fincher, GB
机构
[1] Max Planck Inst Plant Breeding Res, Dept Platn Microbe Interact, D-50892 Cologne, Germany
[2] Univ Adelaide, Australian Ctr Plant Funct Genom, Glen Osmond, SA 5064, Australia
[3] Max Planck Unit Struct Mol Biol, D-22607 Hamburg, Germany
关键词
D O I
10.1105/tpc.016097
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
`Arabidopsis was transformed with double-stranded RNA interference (dsRNAi) constructs designed to silence three putative callose synthase genes: GLUCAN SYNTHASE-LIKE5 (GSL5), GSL6, and GSL11. Both wound callose and papillary callose were absent in lines transformed with GSL5 dsRNAi and in a corresponding sequence-indexed GSL5 T-DNA insertion line but were unaffected in GSL6 and GSL11 dsRNAi lines. These data provide strong genetic evidence that the GSL genes of higher plants encode proteins that are essential for callose formation. Deposition of callosic plugs, or papillae, at sites of fungal penetration is a widely recognized early response of host plants to microbial attack and has been implicated in impeding entry of the fungus. Depletion of callose from papillae in gs15 plants marginally enhanced the penetration of the grass powdery mildew fungus Blumeria graminis on the nonhost Arabidopsis. Paradoxically, the absence of callose, in papillae or haustorial complexes correlated with the effective growth cessation of several normally virulent powdery mildew species and of Peronospora parasitica.
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页码:2503 / 2513
页数:11
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