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  Convergent Losses of TLR5 Suggest Altered Extracellular Flagellin Detection in Four Mammalian Lineages.

Sharma, V., Hecker, N., Walther, F., Stuckas, H., & Hiller, M. (2020). Convergent Losses of TLR5 Suggest Altered Extracellular Flagellin Detection in Four Mammalian Lineages. Molecular biology and evolution, 37(7), 1847-1854. doi:10.1093/molbev/msaa058.

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 Creators:
Sharma, Virag1, Author           
Hecker, Nikolai1, Author           
Walther, Felix, Author
Stuckas, Heiko, Author
Hiller, Michael1, Author           
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Abstract: Toll-like receptors (TLRs) play an important role for the innate immune system by detecting pathogen-associated molecular patterns. TLR5 encodes the major extracellular receptor for bacterial flagellin and frequently evolves under positive selection, consistent with coevolutionary arms races between the host and pathogens. Furthermore, TLR5 is inactivated in several vertebrates and a TLR5 stop codon polymorphism is widespread in human populations. Here, we analyzed the genomes of 120 mammals and discovered that TLR5 is convergently lost in four independent lineages, comprising guinea pigs, Yangtze river dolphin, pinnipeds, and pangolins. Validated inactivating mutations, absence of protein-coding transcript expression, and relaxed selection on the TLR5 remnants confirm these losses. PCR analysis further confirmed the loss of TLR5 in the pinniped stem lineage. Finally, we show that TLR11, encoding a second extracellular flagellin receptor, is also absent in these four lineages. Independent losses of TLR5 and TLR11 suggest that a major pathway for detecting flagellated bacteria is not essential for different mammals and predicts an impaired capacity to sense extracellular flagellin.

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 Dates: 2020-07-01
 Publication Status: Issued
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 Identifiers: DOI: 10.1093/molbev/msaa058
Other: cbg-7642
PMID: 32145026
 Degree: -

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Title: Molecular biology and evolution
  Other : Mol Biol Evol
Source Genre: Journal
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Pages: - Volume / Issue: 37 (7) Sequence Number: - Start / End Page: 1847 - 1854 Identifier: -