Identification and Characterization of a Splicing Variant in the 5′ UTR of the Human TLR5 Gene.

Toll-like receptors (TLRs) are essential components of the innate immune system. TLR5 is the receptor for flagellin, the principal protein component of bacterial flagella. The TLR5 gene has 6 exons. In an RT-PCR analysis, we found long TLR5 transcripts, in addition to those of the expected size (sho...

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Publicado en:BioMed Research International Vol. 2017; pp. 1 - 8
Autores principales: Hoang, Thi Xoan, Duong, Cao Nguyen, Kim, Jae Young
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 8/29/2017
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 8/29/2017
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2017/8727434
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        atl: Identification and Characterization of a Splicing Variant in the 5′ UTR of the Human TLR5 Gene.
      aug:
        au:
          Hoang, Thi Xoan
          Duong, Cao Nguyen
          Kim, Jae Young
        affil: Department of Life Science, Gachon University, Seongnam, Gyeonggi-do 461-701, Republic of Korea
      sug:
        subj:
          Toll-Like Receptors
          Sequence Analysis
          Genes
          Gene Expression
          Human
          Cell Line
          Polymerase Chain Reaction
      ab: Toll-like receptors (TLRs) are essential components of the innate immune system. TLR5 is the receptor for flagellin, the principal protein component of bacterial flagella. The TLR5 gene has 6 exons. In an RT-PCR analysis, we found long TLR5 transcripts, in addition to those of the expected size (short TLR5 transcripts). A sequence analysis revealed that the long TLR5 transcripts contain a new exon of 94 nucleotides located between previously reported exons IV and V in the 5′ untranslated region (5′ UTR). A real-time PCR analysis of the two alternatively spliced variants in various cell lines showed that the long TLR5 transcripts are abundantly expressed in nonimmune cells. The ratios of long/short transcripts in human nonimmune cell lines, such as A549, T98G, HaCaT, H460, HEK-293, and Caco-2 cells, and primary mesenchymal stem cells were in the range of 1.25 to 4.31. In contrast, those of human monocytic THP-1 and U937 cells and E6.1 T cells and Ramos B cells were around 0.9. These ratios in human monocytic THP-1 cells were decreased by treatment with IFN-γ in a concentration-dependent manner. Based on our findings, we suggest that the newly found long TLR5 transcripts may be involved in the negative regulation of TLR5 expression and function.
      pubtype: Academic Journal
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        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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