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鸡第六补体成分的克隆及其 MAC 结构和调控基因的时空表达谱。

Cloning of the sixth complement component and, spatial and temporal expression profile of MAC structural and regulatory genes in chicken.

机构信息

Department of Biology, School of Medicine, University of Patras, Rion 26 500 Patras, Greece.

出版信息

Dev Comp Immunol. 2010 May;34(5):485-90. doi: 10.1016/j.dci.2010.01.003. Epub 2010 Jan 17.

Abstract

Humoral cytotoxicity results from the assembly of terminal components of complement, called membrane attack complex (MAC), which lead to the formation of pores on pathogen membranes. The complement components involved in MAC formation are C5b, C6, C7, C8alpha, C8beta, C8gamma and C9. Among them, C6 protein interacts with C5b through a metastable binding site to form a soluble C5b-6 dimer in the vicinity of the activating cell. Formation of the MAC is controlled by complement regulatory molecules, such as CD59, vitronectin and clusterin. Here, we report the molecular characterization of the C6 complement component, as well as the spatial and temporal expression profile of MAC structural (C6, C7, C8alpha, C8beta, C8gamma) and regulatory (CD59, vitronectin and clusterin) genes in chicken (Gallus gallus). The deduced polypeptide sequence of chicken C6 consists of 935 amino acid residues and exhibits 81%, 58%, 56% and 44% identity with zebra finch, human, frog and trout orthologs, respectively. The 'domain' architecture of chicken C6 resembles that of mammalian counterparts and the cysteine backbone is also conserved. MAC structural and regulatory genes are expressed in a wide range of adult chicken tissues, with the liver being the major source of their produced transcripts. The developmental expression profile of chicken MAC structural genes shows that their transcripts initially appear in the 12th embryonic day in the liver, exhibiting a pick in the 17th, while no expression was detected in the early whole embryo (day 4 and 6), as well as in the 2-day old neonate chicken liver. On the other hand, MAC regulatory genes are expressed in all the developmental stages investigated.

摘要

体液细胞毒性是由补体末端成分的组装引起的,这些成分被称为膜攻击复合物(MAC),导致病原体膜上形成孔。参与 MAC 形成的补体成分包括 C5b、C6、C7、C8alpha、C8beta、C8gamma 和 C9。其中,C6 蛋白通过亚稳定结合位点与 C5b 相互作用,在激活细胞附近形成可溶性 C5b-6 二聚体。MAC 的形成受到补体调节分子的控制,如 CD59、纤连蛋白和斑联蛋白。在这里,我们报告了 C6 补体成分的分子特征,以及 MAC 结构(C6、C7、C8alpha、C8beta、C8gamma)和调节(CD59、纤连蛋白和斑联蛋白)基因在鸡(Gallus gallus)中的时空表达谱。鸡 C6 的推断多肽序列由 935 个氨基酸残基组成,与斑胸草雀、人类、青蛙和鳟鱼的同源物分别具有 81%、58%、56%和 44%的同一性。鸡 C6 的“域”结构与哺乳动物的对应物相似,半胱氨酸骨架也保守。MAC 结构和调节基因在广泛的成年鸡组织中表达,肝脏是其产生转录本的主要来源。鸡 MAC 结构基因的发育表达谱表明,它们的转录本最初在肝脏中出现在第 12 天的胚胎中,在第 17 天出现高峰,而在早期整个胚胎(第 4 天和第 6 天)和 2 天大的新生鸡肝脏中均未检测到。另一方面,MAC 调节基因在所有研究的发育阶段都表达。

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