Large-scale, lineage-specific expansion of a bric-a-brac/tramtrack/broad complex ubiquitin-ligase gene family in rice

被引:94
作者
Gingerich, Derek J.
Hanada, Kousuke
Shiu, Shin-Han
Vierstra, Richard D. [1 ]
机构
[1] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
[2] Michigan State Univ, Dept Plant Biol, E Lansing, MI 48824 USA
关键词
GENOME-WIDE ANALYSIS; F-BOX PROTEINS; PROTEASOME PATHWAY; CELL-DEATH; NUCLEOTIDE SUBSTITUTION; PHYLOGENETIC ANALYSIS; PHOTOTROPIC RESPONSE; POSITIVE SELECTION; ADAPTIVE EVOLUTION; VIRULENCE PROTEIN;
D O I
10.1105/tpc.107.051300
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
Selective ubiquitination of proteins is directed by diverse families of ubiquitin-protein ligases (or E3s) in plants. One important type uses Cullin-3 as a scaffold to assemble multisubunit E3 complexes containing one of a multitude of bric-a-brac/tramtrack/broad complex (BTB) proteins that function as substrate recognition factors. We previously described the 80-member BTB gene superfamily in Arabidopsis thaliana. Here, we describe the complete BTB superfamily in rice (Oryza sativa spp japonica cv Nipponbare) that contains 149 BTB domain-encoding genes and 43 putative pseudogenes. Amino acid sequence comparisons of the rice and Arabidopsis superfamilies revealed a near equal repertoire of putative substrate recognition module types. However, phylogenetic comparisons detected numerous gene duplication and/or loss events since the rice and Arabidopsis BTB lineages split, suggesting possible functional specialization within individual BTB families. In particular, a major expansion and diversification of a subset of BTB proteins containing Meprin and TRAF homology (MATH) substrate recognition sites was evident in rice and other monocots that likely occurred following the monocot/dicot split. The MATH domain of a subset appears to have evolved significantly faster than those in a smaller core subset that predates flowering plants, suggesting that the substrate recognition module in many monocot MATH-BTB E3s are diversifying to ubiquitinate a set of substrates that are themselves rapidly changing. Intriguing possibilities include pathogen proteins attempting to avoid inactivation by the monocot host.
引用
收藏
页码:2329 / 2348
页数:20
相关论文
共 125 条
[101]   The S haplotype-specific F-box protein gene, SFB, is defective in self-compatible haplotypes of Prunus avium and P-mume [J].
Ushijima, K ;
Yamane, H ;
Watari, A ;
Kakehi, E ;
Ikeda, K ;
Hauck, NR ;
Iezzoni, AF ;
Tao, RT .
PLANT JOURNAL, 2004, 39 (04) :573-586
[102]   Protein degradation: CUL-3 and BTB - Partners in proteolysis [J].
van den Heuvel, S .
CURRENT BIOLOGY, 2004, 14 (02) :R59-R61
[103]   Regulated protein degradation [J].
Varshavsky, A .
TRENDS IN BIOCHEMICAL SCIENCES, 2005, 30 (06) :283-286
[104]   The ubiquitin/26S proteasome pathway, the complex last chapter in the life of many plant proteins [J].
Vierstra, RD .
TRENDS IN PLANT SCIENCE, 2003, 8 (03) :135-142
[105]   Evolutionary fate of retroposed gene copies in the human genome [J].
Vinckenbosch, N ;
Dupanloup, I ;
Kaessmann, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (09) :3220-3225
[106]   Mutations in an auxin receptor homolog AFB5 and in SGT1b confer resistance to synthetic picolinate auxins and not to 2,4-dichlorophenoxyacetic acid or indole-3-acetic acid in arabidopsis [J].
Walsh, Terence A. ;
Neal, Roben ;
Merlo, Ann Owens ;
Honma, Mary ;
Hicks, Glenn R. ;
Wolff, Karen ;
Matsumura, Wendy ;
Davies, John P. .
PLANT PHYSIOLOGY, 2006, 142 (02) :542-552
[107]   Regulation of ethylene gas biosynthesis by the Arabidopsis ETO1 protein [J].
Wang, KLC ;
Yoshida, H ;
Lurin, C ;
Ecker, JR .
NATURE, 2004, 428 (6986) :945-950
[108]   Genome-wide analysis of S-Locus F-box-like genes in Arabidopsis thaliana [J].
Wang, L ;
Dong, L ;
Zhang, Y ;
Zhang, YS ;
Wu, WH ;
Deng, XW ;
Xue, YB .
PLANT MOLECULAR BIOLOGY, 2004, 56 (06) :929-945
[109]   Duplication and DNA segmental loss in the rice genome: implications for diploidization [J].
Wang, XY ;
Shi, XL ;
Hao, BL ;
Ge, S ;
Luo, JC .
NEW PHYTOLOGIST, 2005, 165 (03) :937-946
[110]   Arabidopsis AtCUL3a and AtCUL3b form complexes with members of the BTB/POZ-MATH protein family [J].
Weber, H ;
Bernhardt, A ;
Dieterle, M ;
Han, P ;
Hano, P ;
Mutlu, A ;
Estelle, M ;
Genschik, P ;
Hellmann, H .
PLANT PHYSIOLOGY, 2005, 137 (01) :83-93