Post-translational modification of barley 14-3-3A is isoform-specific and involves removal of the hypervariable C-terminus

被引:21
作者
Testerink, C
van Zeijl, MJ
Drumm, K
Palmgren, MG
Collinge, DB
Kijne, JW
Wang, M
机构
[1] Leiden Univ, Netherlands Org Appl Sci Res ULTNO, TNO Dept Appl Plant Sci, Ctr Phytotechnol, NL-2333 AL Leiden, Netherlands
[2] Royal Vet & Agr Univ, Dept Plant Biol, Plant Physiol & Anat Lab, DK-1871 Frederiksberg C, Denmark
[3] Royal Vet & Agr Univ, Dept Plant Biol, Sect Plant Pathol, DK-1871 Frederiksberg C, Denmark
[4] Leiden Univ, Inst Mol Plant Sci,ULTNO, TNO Dept Appl Plant Sci, Ctr Phytotechnol, NL-2333 AL Leiden, Netherlands
关键词
14-3-3; protein; H+-ATPase; Hordeum distichum; post-translational modification; proteolytic cleavage;
D O I
10.1023/A:1019869900285
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
The 14-3-3 protein family is a family of regulatory proteins involved in diverse cellular processes. In a previous study of regulation of individual 14-3-3 isoforms in the germinating barley embryo, we found that a post-translationally modified, 28 kDa form of 14-3-3A was present in specific cell fractions of the germinated embryo. In the present study, we identify the nature of the modification of 14-3-3A, and show that the 28 kDa doublet is the result of cleavage of the C-terminus. The 28 kDa forms of 14-3-3A lack ten or twelve amino acid residues at the non-conserved C-terminus of the protein, respectively. Barley 14-3-3B and 14-3-3C are. not modified in a similar way. Like the 30 kDa form, in vitro produced 28 kDa 14-3-3A is still capable of binding AHA2 H+-ATPase in an overlay assay. Our results show a novel isoform-specific post-translational modification of 14-3-3 proteins that is regulated in a tissue-specific and developmental way.
引用
收藏
页码:535 / 542
页数:8
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