Two naturally occurring deletion mutants of 12S seed storage proteins in Arabidopsis thaliana

被引:0
|
作者
Anfu Hou
Kede Liu
Niramol Catawatcharakul
Xurong Tang
Vi Nguyen
Wilfred A. Keller
Edward W. T. Tsang
Yuhai Cui
机构
[1] Agriculture and Agri-Food Canada,Southern Crop Protection and Food Research Centre
[2] Huazhong Agriculture University,National Key Laboratory of Crop Genetic Improvement
[3] National Research Council of Canada,Plant Biotechnology Institute
来源
Planta | 2005年 / 222卷
关键词
Deletion mutants; Mass spectrometry; Natural variations; Seed storage proteins;
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摘要
Two naturally occurring Arabidopsis mutants, Cape Verde Islands and Monte (Mr-0), with aberrant 12S seed storage protein (SSP) profiles have been identified by SDS-PAGE. In both mutants, one of the 12S globulin bands is missing while a new band of lower molecular mass is present. Tandem mass spectrometry-mass spectrometry (MS/MS) analyses of the mutant peptides have revealed that both are shorter variants of 12S globulin with deletion sites detected within the α-subunits of 12S globulin cruciferin B (CRB) and C (CRC), respectively. Sequence analyses of the genomic DNA flanking the deletion sites have demonstrated that both deletions occurred at the genomic level. These two mutants are referred to as CRBΔ12 and CRCΔ13 with the delta sign indicating a deletion and the number indicating amino acids deleted. Alignment of these two mutant sequences with that of soybean A3B4 subunit, for which the crystal structure was determined recently, have revealed that the CRCΔ13 deletion is located in a hypervariable/disordered region, and will probably not affect the structure of the hexameric globulin. The CRBΔ12 deletion, however, is located in a binding region that is thought to be important for the hexamer formation. However, CRBΔ12 appears to accumulate normally as judged by its band intensity relative to the other SSP subunits on the protein gels. Thus it seems that the seed can, to a certain extent, tolerate some mutations in its storage proteins.
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页码:512 / 520
页数:8
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