Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary properties

被引:244
作者
Sardiello, Marco [1 ]
Cairo, Stefano [1 ,3 ]
Fontanella, Bianca [1 ,4 ]
Ballabio, Andrea [1 ,2 ]
Meroni, Germana [1 ]
机构
[1] TIGEM, I-80131 Naples, Italy
[2] Univ Naples Federico 2, Dept Pediat, I-80131 Naples, Italy
[3] Inst Pasteur, Unite Oncogenese & Virol Mol, F-75724 Paris 15, France
[4] Univ Salerno, Dept Pharmaceut Sci, I-84084 Fisciano, SA, Italy
关键词
D O I
10.1186/1471-2148-8-225
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The TRIM family is composed of multi-domain proteins that display the Tripartite Motif (RING, B-box and Coiled-coil) that can be associated with a C-terminal domain. TRIM genes are involved in ubiquitylation and are implicated in a variety of human pathologies, from Mendelian inherited disorders to cancer, and are also involved in cellular response to viral infection. Results: Here we defined the entire human TRIM family and also identified the TRIM sets of other vertebrate (mouse, rat, dog, cow, chicken, tetraodon, and zebrafish) and invertebrate species (fruitfly, worm, and ciona). By means of comparative analyses we found that, after assembly of the tripartite motif in an early metazoan ancestor, few types of C-terminal domains have been associated with this module during evolution and that an important increase in TRIM number occurred in vertebrate species concomitantly with the addition of the SPRY domain. We showed that the human TRIM family is split into two groups that differ in domain structure, genomic organization and evolutionary properties. Group 1 members present a variety of C-terminal domains, are highly conserved among vertebrate species, and are represented in invertebrates. Conversely, group 2 is absent in invertebrates, is characterized by the presence of a C-terminal SPRY domain and presents unique sets of genes in each mammal examined. The generation of independent sets of group 2 genes is also evident in the other vertebrate species. Comparing the murine and human TRIM sets, we found that group 1 and 2 genes evolve at different speeds and are subject to different selective pressures. Conclusion: We found that the TRIM family is composed of two groups of genes with distinct evolutionary properties. Group 2 is younger, highly dynamic, and might act as a reservoir to develop novel TRIM functions. Since some group 2 genes are implicated in innate immune response, their evolutionary features may account for species-specific battles against viral infection.
引用
收藏
页数:22
相关论文
共 68 条
[1]   A retrovirus restriction factor TRIM5α is transcriptionally regulated by interferons [J].
Asaoka, K ;
Ikeda, K ;
Hishinuma, T ;
Horie-Inoue, K ;
Takeda, S ;
Inoue, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 338 (04) :1950-1956
[2]   Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism [J].
Avela, K ;
Lipsanen-Nyman, M ;
Idänheimo, N ;
Seemanová, E ;
Rosengren, S ;
Mäkelä, TP ;
Perheentupa, J ;
de la Chapelle, A ;
Lehesjoki, AE .
NATURE GENETICS, 2000, 25 (03) :298-301
[3]  
Bernot A, 1997, NAT GENET, V17, P25
[4]   Cyclophilin A is required for TRIM5α-mediated resistance to HIV-1 in old world monkey cells [J].
Berthoux, L ;
Sebastian, S ;
Sokolskaja, E ;
Luban, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (41) :14849-14853
[5]   Identification of ubiquitin ligases required for skeletal muscle atrophy [J].
Bodine, SC ;
Latres, E ;
Baumhueter, S ;
Lai, VKM ;
Nunez, L ;
Clarke, BA ;
Poueymirou, WT ;
Panaro, FJ ;
Na, EQ ;
Dharmarajan, K ;
Pan, ZQ ;
Valenzuela, DM ;
DeChiara, TM ;
Stitt, TN ;
Yancopoulos, GD ;
Glass, DJ .
SCIENCE, 2001, 294 (5547) :1704-1708
[6]   NOVEL TOPOLOGY OF A ZINC-BINDING DOMAIN FROM A PROTEIN INVOLVED IN REGULATING EARLY XENOPUS DEVELOPMENT [J].
BORDEN, KLB ;
LALLY, JM ;
MARTIN, SR ;
OREILLY, NJ ;
ETKIN, LD ;
FREEMONT, PS .
EMBO JOURNAL, 1995, 14 (23) :5947-5956
[7]   THE SOLUTION STRUCTURE OF THE RING FINGER DOMAIN FROM THE ACUTE PROMYELOCYTIC LEUKEMIA PROTO-ONCOPROTEIN PML [J].
BORDEN, KLB ;
BODDY, MN ;
LALLY, J ;
OREILLY, NJ ;
MARTIN, S ;
HOWE, K ;
SOLOMON, E ;
FREEMONT, PS .
EMBO JOURNAL, 1995, 14 (07) :1532-1541
[8]   Homozygosity mapping with SNP arrays identifies TRIM32 an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11) [J].
Chiang, AP ;
Beck, JS ;
Yen, HJ ;
Tayeh, MK ;
Scheetz, TE ;
Swiderski, RE ;
Nishimura, DY ;
Braun, TA ;
Kim, KYA ;
Huang, J ;
Elbedour, K ;
Carmi, R ;
Slusarski, DC ;
Casavant, TL ;
Stone, EM ;
Sheffield, VC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (16) :6287-6292
[9]   Characterization of BT3 molecules belonging to the B7 family expressed on immune cells [J].
Compte, E ;
Pontarotti, P ;
Collette, Y ;
Lopez, M ;
Olive, D .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (08) :2089-2099
[10]  
CONSORTIUM TIF, 1997, CELL, V90, P797, DOI DOI 10.1016/S0092-8674(00)80539-5