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猪(野猪)中细胞因子TWEAK及其受体Fn14的分子特征

Molecular characterization of cytokine TWEAK and its receptor Fn14 in pig (Sus scrofa).

作者信息

Shui Yan, Guan Zheng-Bing, Zhang Shuang-Quan

机构信息

Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology, Life Sciences College, Nanjing Normal University, Nanjing 210046, PR China.

出版信息

Vet Immunol Immunopathol. 2008 Dec 15;126(3-4):396-402. doi: 10.1016/j.vetimm.2008.08.005. Epub 2008 Aug 23.

DOI:10.1016/j.vetimm.2008.08.005
PMID:18817982
Abstract

Tumor necrosis factor-like weak inducer of apoptosis (TWEAK) is a member of the tumor necrosis factor superfamily (TNFSF). The interaction of TWEAK with its receptor fibroblast growth factor-inducible 14 (Fn14) regulates multiple cellular responses, including stimulation of proliferation, migration, apoptosis, angiogenesis, and induction of proinflammatory cytokines. This paper reports for the first time the molecular cloning of porcine TWEAK and Fn14 by EST and RACE strategies. The full-length cDNA of porcine TWEAK is 1327bp, including an open reading frame (ORF) of 747bp. Its genomic DNA consists of seven exons and six introns and is approximately 10kb in size by computer-assisted analysis. Sequence similarity at the amino acid level between porcine TWEAK and human or mouse was 95 and 92%, respectively. The full-length cDNA of porcine Fn14 contains 691bp, of which 390bp are the ORF. Sequence similarity at the amino acid level between porcine Fn14 and human, or mouse, or frog was 95, 93 and 64%, respectively. Real-time quantitative PCR (Q-PCR) analysis revealed that both TWEAK and Fn14 are constitutively expressed in various tissues in pig. Our results suggest that the TWEAK-Fn14 pathway is evolutionarily highly conserved. It will be helpful for investigation on the biological role of the TWEAK/Fn14 system in this important animal model. Furthermore, it provides insight into the molecular evolution of the emerging TWEAK and Fn14 families.

摘要

肿瘤坏死因子样凋亡微弱诱导剂(TWEAK)是肿瘤坏死因子超家族(TNFSF)的成员。TWEAK与其受体成纤维细胞生长因子诱导14(Fn14)的相互作用调节多种细胞反应,包括刺激增殖、迁移、凋亡、血管生成以及诱导促炎细胞因子。本文首次通过EST和RACE策略报道了猪TWEAK和Fn14的分子克隆。猪TWEAK的全长cDNA为1327bp,包括一个747bp的开放阅读框(ORF)。通过计算机辅助分析,其基因组DNA由7个外显子和6个内含子组成,大小约为10kb。猪TWEAK与人或小鼠在氨基酸水平上的序列相似性分别为95%和92%。猪Fn14的全长cDNA包含691bp,其中390bp为ORF。猪Fn14与人、小鼠或青蛙在氨基酸水平上的序列相似性分别为95%、93%和64%。实时定量PCR(Q-PCR)分析显示,TWEAK和Fn14在猪的各种组织中均组成性表达。我们的结果表明,TWEAK-Fn14途径在进化上高度保守。这将有助于在这个重要的动物模型中研究TWEAK/Fn14系统的生物学作用。此外,它还为新兴的TWEAK和Fn14家族的分子进化提供了见解。

相似文献

1
Molecular characterization of cytokine TWEAK and its receptor Fn14 in pig (Sus scrofa).猪(野猪)中细胞因子TWEAK及其受体Fn14的分子特征
Vet Immunol Immunopathol. 2008 Dec 15;126(3-4):396-402. doi: 10.1016/j.vetimm.2008.08.005. Epub 2008 Aug 23.
2
Molecular characterization of the canine cytokine TWEAK (CD255) and its receptor, Fn14 (CD266).犬细胞因子TWEAK(CD255)及其受体Fn14(CD266)的分子特征
Vet Immunol Immunopathol. 2010 Sep 15;137(1-2):172-5. doi: 10.1016/j.vetimm.2010.04.004. Epub 2010 Apr 14.
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Molecular structure and characterization of the cytokine TWEAK and its receptor Fn14 in bovine.牛细胞因子TWEAK及其受体Fn14的分子结构与特性
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Proinflammatory effects of tumour necrosis factor-like weak inducer of apoptosis (TWEAK) on human gingival fibroblasts.肿瘤坏死因子样凋亡微弱诱导剂(TWEAK)对人牙龈成纤维细胞的促炎作用
Clin Exp Immunol. 2006 Dec;146(3):540-9. doi: 10.1111/j.1365-2249.2006.03233.x.
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TWEAK/Fn14 interaction regulates RANTES production, BMP-2-induced differentiation, and RANKL expression in mouse osteoblastic MC3T3-E1 cells.TWEAK/Fn14相互作用调节小鼠成骨MC3T3-E1细胞中RANTES的产生、BMP-2诱导的分化及RANKL的表达。
Arthritis Res Ther. 2006;8(5):R146. doi: 10.1186/ar2038.
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TWEAK/Fn14 promotes apoptosis of human endometrial cancer cells via caspase pathway.TWEAK/Fn14 通过半胱天冬酶途径促进人子宫内膜癌细胞凋亡。
Cancer Lett. 2010 Aug 1;294(1):91-100. doi: 10.1016/j.canlet.2010.01.027. Epub 2010 Feb 26.
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TWEAK and Fn14: new molecular targets for cancer therapy?肿瘤坏死因子样弱凋亡诱导因子(TWEAK)与Fn14:癌症治疗的新分子靶点?
Cancer Lett. 2006 Apr 8;235(1):11-7. doi: 10.1016/j.canlet.2005.03.048.
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TWEAK/Fn14 pathway: a nonredundant role in intestinal damage in mice through a TWEAK/intestinal epithelial cell axis.TWEAK/Fn14信号通路:通过TWEAK/肠上皮细胞轴在小鼠肠道损伤中发挥非冗余作用。
Gastroenterology. 2009 Mar;136(3):912-23. doi: 10.1053/j.gastro.2008.11.017. Epub 2008 Nov 8.
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Tumour necrosis factor-like weak inducer of apoptosis (TWEAK) and its receptor Fn14 during cardiac remodelling in rats.肿瘤坏死因子样凋亡微弱诱导因子(TWEAK)及其受体 Fn14 在大鼠心脏重构中的作用。
Acta Physiol (Oxf). 2010 May;199(1):11-22. doi: 10.1111/j.1748-1716.2010.02080.x. Epub 2010 Jan 16.
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TWEAKing tissue remodeling by a multifunctional cytokine: role of TWEAK/Fn14 pathway in health and disease.多功能细胞因子调节组织重塑:TWEAK/Fn14信号通路在健康与疾病中的作用
Cytokine. 2007 Oct;40(1):1-16. doi: 10.1016/j.cyto.2007.09.007. Epub 2007 Nov 5.

引用本文的文献

1
Full-length, membrane-anchored TWEAK can function as a juxtacrine signaling molecule and activate the NF-kappaB pathway.全长型、膜锚定的 TWEAK 可以作为旁分泌信号分子发挥作用,并激活 NF-κB 通路。
J Biol Chem. 2010 Jun 4;285(23):17432-41. doi: 10.1074/jbc.M110.131979. Epub 2010 Apr 12.