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Pig lacks functional NLRC4 and NAIP genes

Authors :
Hiroki Shinkai
Daisuke Toki
Takato Takenouchi
Hiroshi Kitani
Mitsuru Sato
Hirohide Uenishi
Chisato Sakuma
Source :
SC30201802140027, NARO成果DBa, This is a post-peer-review, pre-copyedit version of an article published in [Immunogenetics]., The final authenticated version is available online at: http://dx.doi.org/10.1007/s00251-016-0955-5, This is not the published version. Please cite only the published version., この論文は出版社版ではありません。引用の際には出版社版をご利用ください。
Publication Year :
2017
Publisher :
Published by Springer Berlin Heidelberg, 2017.

Abstract

The NLRC4 inflammasome, which recognizes flagellin and components of the type III secretion system, plays an important role in the clearance of intracellular bacteria. Here, we examined the genomic sequences carrying two genes encoding key components of the NLRC4 inflammasome-NLR family, CARD-containing 4 (NLRC4), and NLR apoptosis inhibitory protein (NAIP)-in pigs. Pigs have a single locus encoding NLRC4 and NAIP. Comparison of the sequences thus obtained with the corresponding regions in humans revealed the deletion of intermediate exons in both pig genes. In addition, the genomic sequences of both pig genes lacked valid open reading frames encoding functional NLRC4 or NAIP protein. Additional pigs representing multiple breeds and wild boars also lacked the exons that we failed to find through genome sequencing. Furthermore, neither the NLRC4 nor the NAIP gene was expressed in pigs. These findings indicate that pigs lack the NLRC4 inflammasome, an important factor involved in monitoring bacterial proteins and contributing to the clearance of intracellular pathogens. These results also suggest that genetic polymorphisms affecting the molecular functions of TLR2, TLR4, TLR5, and other pattern recognition receptors associated with the recognition of bacteria have a more profound influence on disease resistance in pigs than in other species.

Details

Language :
English
ISSN :
14321211
Volume :
69
Issue :
2
Database :
OpenAIRE
Journal :
Immunogenetics = Immunogenetics
Accession number :
edsair.doi.dedup.....b72fbaa844c24d89bcef6cdfa14656f0
Full Text :
https://doi.org/10.1007/s00251-016-0955-5