2015Journal of Northwest A&F UniversityRequires access

Expression analysis of TLR1 gene in different tissues of Maiwa yak

Yabin Chen

Open publisher page 0 citations

Abstract

【Objective】The study was designed to establish a real-time PCR assay for detection of TLR1 gene,and to further analyze the expression pattern in tissues of yaks.【Method】According to the sequence of yak TLR1 gene,the real-time PCR primers were designed,the real-time PCR was established,and theβ-actin gene was chosen to normalize the expression level of TLR1 gene.The established detection method was used to analyze the expression pattern of TLR1 gene in different tissues of yak,including heart,liver,spleen,lung,kidney,large intestine,small intestine,stomach,mammary gland,muscle and ovary.【Result】The electrophoresis results showed that both TLR1 gene andβ-actin gene included a signal band.The melting curve of target product showed that the product was specific to a single peak,suggesting the specificity of primers.Moreover,real-time quantitative PCR assay was established and used to detect the relative expression level of TLR1 gene in different tissues,and the gene expression level in small intestine was selected as a baseline.The quantitative results showed that TLR1 gene was expressed at eleven tissues examined.TLR1 gene had high expression levels in kidney,liver,spleen,lung,ovary,small intestine and low levels in stomach,mammary gland,heart,large intestine and muscle.【Conclusion】There were differences on the transcription levels of TLR1 mRNA in different tissues,which may be associated with the ability to recognize and defend pathogens for different tissues.

About this research paper

What this paper is about

【Objective】The study was designed to establish a real-time PCR assay for detection of TLR1 gene,and to further analyze the expression pattern in tissues of yaks.【Method】According to the sequence of yak TLR1 gene,the real-time PCR primers were designed,the real-time PCR was established,and theβ-actin gene was chosen to normalize the expression level of TLR1 gene.The established detection method was used to analyze the expression pattern of TLR1 gene in different tissues of yak,including heart,liver,spleen,lung,kidney,large intestine,small intestine,stomach,mammary gland,muscle and ovary.【Result】The electrophoresis results showed that both TLR1 gene andβ-actin gene included a signal band.The melting curve of target product showed that the product was specific to a single peak,suggesting the specificity of primers.Moreover,real-time quantitative PCR assay was established and used to detect the relative expression level of TLR1 gene in different tissues,and the gene expression level in small intestine was selected as a baseline.The quantitative results showed that TLR1 gene was expressed at eleven tissues examined.TLR1 gene had high expression levels in kidney,liver,spleen,lung,ovary,small intestine and low levels in stomach,mammary gland,heart,large intestine and muscle.【Conclusion】There were differences on the transcription levels of TLR1 mRNA in different tissues,which may be associated with the ability to recognize and defend pathogens for different tissues.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

【Objective】The study was designed to establish a real-time PCR assay for detection of TLR1 gene,and to further analyze the expression pattern in tissues of yaks.【Method】According to the sequence of yak TLR1 gene,the real-time PCR primers were designed,the real-time PCR was established,and theβ-actin gene was chosen to normalize the expression level of TLR1 gene.The established detection method was used to analyze the expression pattern of TLR1 gene in different tissues of yak,including heart,liver,spleen,lung,kidney,large intestine,small intestine,stomach,mammary gland,muscle and ovary.【Result】The electrophoresis results showed that both TLR1 gene andβ-actin gene included a signal band.The melting curve of target product showed that the product was specific to a single peak,suggesting the specificity of primers.Moreover,real-time quantitative PCR assay was established and used to detect the relative expression level of TLR1 gene in different tissues,and the gene expression level in small intestine was selected as a baseline.The quantitative results showed that TLR1 gene was expressed at eleven tissues examined.TLR1 gene had high expression levels in kidney,liver,spleen,lung,ovary,small intestine and low levels in stomach,mammary gland,heart,large intestine and muscle.【Conclusion】There were differences on the transcription levels of TLR1 mRNA in different tissues,which may be associated with the ability to recognize and defend pathogens for different tissues.

Key concepts: Gene expression, Biology, Gene, Molecular biology, Real-time polymerase chain reaction, Kidney, Stomach, Spleen

Related papers

Back to paper searchBrowse research topicsOriginal source
Expression analysis of TLR1 gene in different tissues of Maiwa yak — Research Paper | ScholarLens