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

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...

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Autores principales: Matsushima, Norio, Tanaka, Takanori, Enkhbayar, Purevjav, Mikami, Tomoko, Taga, Masae, Yamada, Keiko, Kuroki, Yoshio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1899181/
https://www.ncbi.nlm.nih.gov/pubmed/17517123
http://dx.doi.org/10.1186/1471-2164-8-124
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author Matsushima, Norio
Tanaka, Takanori
Enkhbayar, Purevjav
Mikami, Tomoko
Taga, Masae
Yamada, Keiko
Kuroki, Yoshio
author_facet Matsushima, Norio
Tanaka, Takanori
Enkhbayar, Purevjav
Mikami, Tomoko
Taga, Masae
Yamada, Keiko
Kuroki, Yoshio
author_sort Matsushima, Norio
collection PubMed
description 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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spelling pubmed-18991812007-06-26 Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors Matsushima, Norio Tanaka, Takanori Enkhbayar, Purevjav Mikami, Tomoko Taga, Masae Yamada, Keiko Kuroki, Yoshio BMC Genomics Research Article 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. BioMed Central 2007-05-21 /pmc/articles/PMC1899181/ /pubmed/17517123 http://dx.doi.org/10.1186/1471-2164-8-124 Text en Copyright © 2007 Matsushima et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Matsushima, Norio
Tanaka, Takanori
Enkhbayar, Purevjav
Mikami, Tomoko
Taga, Masae
Yamada, Keiko
Kuroki, Yoshio
Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors
title Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors
title_full Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors
title_fullStr Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors
title_full_unstemmed Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors
title_short Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors
title_sort comparative sequence analysis of leucine-rich repeats (lrrs) within vertebrate toll-like receptors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1899181/
https://www.ncbi.nlm.nih.gov/pubmed/17517123
http://dx.doi.org/10.1186/1471-2164-8-124
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