Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors

被引:305
作者
Matsushima, Norio [1 ]
Tanaka, Takanori
Enkhbayar, Purevjav
Mikami, Tomoko
Taga, Masae
Yamada, Keiko
Kuroki, Yoshio
机构
[1] Sapporo Med Univ, Sch Hlth Sci, Sapporo, Hokkaido 0608556, Japan
[2] RIKEN, Genom Sci Ctr, Yokohama, Kanagawa 2300045, Japan
[3] Natl Univ Mongolia, Fac Biol, Ulaanbaatar 210646 377, Mongolia
[4] Sapporo City Univ, Dept Nursing, Sapporo, Hokkaido 0600011, Japan
[5] Sapporo Med Univ, Sch Med, Dept Biochem, Sapporo, Hokkaido 0608556, Japan
关键词
D O I
10.1186/1471-2164-8-124
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Toll-like receptors (TLRs) play a central role in innate immunity. TLRs are membrane glycoproteins and contain leucine rich repeat (LRR) motif in the ectodomain. TLRs recognize and respond to molecules such as lipopolysaccharide, peptidoglycan, flagellin, and RNA from bacteria or viruses. The LRR domains in TLRs have been inferred to be responsible for molecular recognition. All LRRs include the highly conserved segment, LxxLxLxxNxL, in which "L" is Leu, Ile, Val, or Phe and "N" is Asn, Thr, Ser, or Cys and "x" is any amino acid. There are seven classes of LRRs including "typical" ("T") and " bacterial" ("S"). All known domain structures adopt an arc or horseshoe shape. Vertebrate TLRs form six major families. The repeat numbers of LRRs and their "phasing" in TLRs differ with isoforms and species; they are aligned differently in various databases. We identified and aligned LRRs in TLRs by a new method described here. Results: The new method utilizes known LRR structures to recognize and align new LRR motifs in TLRs and incorporates multiple sequence alignments and secondary structure predictions. TLRs from thirty-four vertebrate were analyzed. The repeat numbers of the LRRs ranges from 16 to 28. The LRRs found in TLRs frequently consists of LxxLxLxxNxLxxLxxxxF/LxxLxx ("T") and sometimes short motifs including LxxLxLxxNxLxxLPx(x) LPxx ("S"). The TLR7 family (TLR7, TLR8, and TLR9) contain 27 LRRs. The LRRs at the N-terminal part have a super-motif of STT with about 80 residues. The super-repeat is represented by STTSTTSTT or _TTSTTSTT. The LRRs in TLRs form one or two horseshoe domains and are mostly flanked by two cysteine clusters including two or four cysteine residue. Conclusion: Each of the six major TLR families is characterized by their constituent LRR motifs, their repeat numbers, and their patterns of cysteine clusters. The central parts of the TLR1 and TLR7 families and of TLR4 have more irregular or longer LRR motifs. These central parts are inferred to play a key role in the structure and/or function of their TLRs. Furthermore, the super-repeat in the TLR7 family suggests strongly that " bacterial" and "typical" LRRs evolved from a common precursor.
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页数:20
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共 79 条
[21]   Structural basis of the Cks1-dependent recognition of p27Kip1 by the SCFSkp2 ubipuitin ligase [J].
Hao, B ;
Zheng, N ;
Schulman, BA ;
Wu, G ;
Miller, JJ ;
Pagano, M ;
Pavletich, NP .
MOLECULAR CELL, 2005, 20 (01) :9-19
[22]   Structure of the Nogo receptor ectodomain: A recognition module implicated in myelin inhibition [J].
He, XLL ;
Bazan, JF ;
McDermott, G ;
Park, JB ;
Wang, K ;
Tessier-Lavigne, M ;
He, ZG ;
Garcia, KC .
NEURON, 2003, 38 (02) :177-185
[23]   A missense mutation of the Toll-like receptor 3 gene in a patient with influenza-associated encephalopathy [J].
Hidaka, F ;
Matsuo, S ;
Muta, T ;
Takeshige, K ;
Mizukami, T ;
Nunoi, H .
CLINICAL IMMUNOLOGY, 2006, 119 (02) :188-194
[24]   The crystal structure of rna1p: A new fold for a GTPase-activating protein [J].
Hillig, RC ;
Renault, L ;
Vetter, IR ;
Drell, T ;
Wittinghofer, A ;
Becker, J .
MOLECULAR CELL, 1999, 3 (06) :781-791
[25]   Characterization of gene structure and expression of two toll-like receptors from Japanese flounder, Paralichthys olivaceus [J].
Hirono, I ;
Takami, M ;
Miyata, M ;
Miyazaki, T ;
Han, HJ ;
Takano, T ;
Endo, M ;
Aoki, T .
IMMUNOGENETICS, 2004, 56 (01) :38-46
[26]   The crystal structure and mutational analysis of a novel RNA-binding domain found in the human Tap nuclear mRNA export factor [J].
Ho, DN ;
Coburn, GA ;
Kang, YB ;
Cullen, BR ;
Georgiadis, MM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :1888-1893
[27]   Binding site for Robo receptors revealed by dissection of the leucine-rich repeat region of Slit [J].
Howitt, JA ;
Clout, NJ ;
Hohenester, E .
EMBO JOURNAL, 2004, 23 (22) :4406-4412
[28]   Structures of glycoprotein Ibα and its complex with von Willebrand factor A1 domain [J].
Huizinga, EG ;
Tsuji, S ;
Romijn, RAP ;
Schiphorst, ME ;
de Groot, PG ;
Sixma, JJ ;
Gros, P .
SCIENCE, 2002, 297 (5584) :1176-1179
[29]   Toll-like receptor function and signaling [J].
Kaisho, Tsuneyasu ;
Akira, Shizuo .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 117 (05) :979-987
[30]   Structural diversity of leucine-rich repeat proteins [J].
Kajava, AV .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 277 (03) :519-527