Molecular Cloning and Functional Analysis of the Duck TLR4 Gene

Toll-like receptor 4 (TLR4) recognizes pathogen-associated molecular patterns in some animals and has been shown to be closely associated with several diseases such as tumors, atherosclerosis, and asthma. However, its function in ducks is not clear. Alternative splicing of the TLR4 gene has been ide...

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Main Authors: Chunyu Mu, Qi Xu, Guohong Chen, Guanghui Rong, Yang Zhang, Yang Chen, Wenming Zhao, Zhengyang Huang
Format: Article
Language:English
Published: MDPI AG 2013-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/14/9/18615
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spelling doaj-edf0e59a547d4b088fbd3c451d962b732020-11-24T21:01:37ZengMDPI AGInternational Journal of Molecular Sciences1422-00672013-09-01149186151862810.3390/ijms140918615Molecular Cloning and Functional Analysis of the Duck TLR4 GeneChunyu MuQi XuGuohong ChenGuanghui RongYang ZhangYang ChenWenming ZhaoZhengyang HuangToll-like receptor 4 (TLR4) recognizes pathogen-associated molecular patterns in some animals and has been shown to be closely associated with several diseases such as tumors, atherosclerosis, and asthma. However, its function in ducks is not clear. Alternative splicing of the TLR4 gene has been identified in pigs, sheep, mice, and other species, but has not yet been reported in the duck. In this study, alternative splicing of the duck TLR4 gene was investigated using reverse transcription-polymerase chain reaction (RT-PCR). Duck TLR4 gene (duTLR4, accession number: KF278109) was found to consist of 3367 nucleotides of coding sequence. An alternative splice form, TLR4-b, was identified and shown by alignment to retain the intron between exons 1 and 2. Real-time quantitative polymerase chain reaction (qPCR) analyses suggested that duTLR4-a (wild-type) mRNA is widely expressed in various healthy tissues, whereas TLR4-b is expressed at only low levels. Following stimulation of normal duck embryo fibroblasts with lipopolysaccharide, the expression of both isoforms initially increased and then decreased. Expression of the wild-type isoform subsequently increased again, while that of the variant remained low. The expression levels of wild-type TLR4 were further analyzed by transient transfection of a pcDNA3.1(+)-TLR4-a overexpression vector into duck embryo fibroblasts. qRT-PCR analyses showed that after stimulation with LPS and poly(I:C) the expression levels of IL-1β, IL6, and MHC II increased with a response-efficacy relationship. Our experimental results indicate that TLR4 plays an important role in resistance to both bacterial and viral infections in the duck.http://www.mdpi.com/1422-0067/14/9/18615duckTLR4alternative splicingexpression analysis
collection DOAJ
language English
format Article
sources DOAJ
author Chunyu Mu
Qi Xu
Guohong Chen
Guanghui Rong
Yang Zhang
Yang Chen
Wenming Zhao
Zhengyang Huang
spellingShingle Chunyu Mu
Qi Xu
Guohong Chen
Guanghui Rong
Yang Zhang
Yang Chen
Wenming Zhao
Zhengyang Huang
Molecular Cloning and Functional Analysis of the Duck TLR4 Gene
International Journal of Molecular Sciences
duck
TLR4
alternative splicing
expression analysis
author_facet Chunyu Mu
Qi Xu
Guohong Chen
Guanghui Rong
Yang Zhang
Yang Chen
Wenming Zhao
Zhengyang Huang
author_sort Chunyu Mu
title Molecular Cloning and Functional Analysis of the Duck TLR4 Gene
title_short Molecular Cloning and Functional Analysis of the Duck TLR4 Gene
title_full Molecular Cloning and Functional Analysis of the Duck TLR4 Gene
title_fullStr Molecular Cloning and Functional Analysis of the Duck TLR4 Gene
title_full_unstemmed Molecular Cloning and Functional Analysis of the Duck TLR4 Gene
title_sort molecular cloning and functional analysis of the duck tlr4 gene
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2013-09-01
description Toll-like receptor 4 (TLR4) recognizes pathogen-associated molecular patterns in some animals and has been shown to be closely associated with several diseases such as tumors, atherosclerosis, and asthma. However, its function in ducks is not clear. Alternative splicing of the TLR4 gene has been identified in pigs, sheep, mice, and other species, but has not yet been reported in the duck. In this study, alternative splicing of the duck TLR4 gene was investigated using reverse transcription-polymerase chain reaction (RT-PCR). Duck TLR4 gene (duTLR4, accession number: KF278109) was found to consist of 3367 nucleotides of coding sequence. An alternative splice form, TLR4-b, was identified and shown by alignment to retain the intron between exons 1 and 2. Real-time quantitative polymerase chain reaction (qPCR) analyses suggested that duTLR4-a (wild-type) mRNA is widely expressed in various healthy tissues, whereas TLR4-b is expressed at only low levels. Following stimulation of normal duck embryo fibroblasts with lipopolysaccharide, the expression of both isoforms initially increased and then decreased. Expression of the wild-type isoform subsequently increased again, while that of the variant remained low. The expression levels of wild-type TLR4 were further analyzed by transient transfection of a pcDNA3.1(+)-TLR4-a overexpression vector into duck embryo fibroblasts. qRT-PCR analyses showed that after stimulation with LPS and poly(I:C) the expression levels of IL-1β, IL6, and MHC II increased with a response-efficacy relationship. Our experimental results indicate that TLR4 plays an important role in resistance to both bacterial and viral infections in the duck.
topic duck
TLR4
alternative splicing
expression analysis
url http://www.mdpi.com/1422-0067/14/9/18615
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