The N-terminal tetra-peptide (IPDE) short extension of the U-box motif in rice SPL11 E3 is essential for the interaction with E2 and ubiquitin-ligase activity

被引:20
作者
Bae, Hansol [1 ]
Kim, Woo Taek [1 ]
机构
[1] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Syst Biol, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
E2 Ub-conjugating enzyme; E3; Ub-ligase; Rice (Olyza sativa L.); U-box motif; E2-E3; interaction; Ubiquitination; MEDIATED DROUGHT STRESS; ABSCISIC-ACID; BIOCHEMICAL FUNCTION; PROTEASOME SYSTEM; COMBINATORY ROLES; ARABIDOPSIS; RESPONSES; DOMAIN; ENZYMES; PLANTS;
D O I
10.1016/j.bbrc.2013.03.005
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
Rice, a monocot model plant, contains at least 77 U-box E3 ubiquitin (Ub)-ligases and 48 E2 Ub-conjugating enzymes. Here, we investigated the minimal binding domain of rice SPL11 U-box E3 to its E2 partners. Serial deletions and site-directed mutagenesis analyses indicated that, in addition to an intact U-box motif, the N-terminal tetra-peptide (IPDE) short extension of the U-box was essential for the interaction of SPL11 with E2s and Ub-ligase activity. The Ile and Pro residues at the -4 and -3 positions of the U-box, respectively, were crucial for this interaction. These results suggest that the N-terminal tetra-peptide extension of the U-box participates in the specific interaction of SPL11 E3 with E2s in a sequence-specific manner in rice. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:266 / 271
页数:6
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