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黑猩猩和食蟹猕猴中白细胞介素-4 δ2剪接变体(IL-4δ2)的克隆:δ2剪接变体出现的系统发育分析及其对IL-4驱动的免疫过程研究的意义

Cloning of interleukin-4 delta2 splice variant (IL-4delta2) in chimpanzee and cynomolgus macaque: phylogenetic analysis of delta2 splice variant appearance, and implications for the study of IL-4-driven immune processes.

作者信息

Gautherot Isabelle, Burdin Nicolas, Seguin Delphine, Aujame Luc, Sodoyer Régis

机构信息

Research Department, Molecular Biology Section, Aventis Pasteur, Campus Mérieux, 1541 avenue Marcel Mérieux, 69280 Marcy l'Etoile, France.

出版信息

Immunogenetics. 2002 Dec;54(9):635-44. doi: 10.1007/s00251-002-0510-4. Epub 2002 Nov 12.

Abstract

The human interleukin-4 ( IL-4) gene produces an exon 2-lacking alternative splice variant, termed IL-4delta2, and described as a naturally occurring antagonist of IL-4-driven activity. We report the isolation of an IL-4delta2 cDNA from chimpanzee ( Pan troglodytes) bone marrow samples and cynomolgus macaque ( Macaca fascicularis) activated peripheral lymph node cells. The complete IL-4 cDNA sequence from chimpanzee is also provided for the first time. The phylogenetic analysis of several known IL-4 sequences revealed a highly conserved structure of coding regions among primates, suggesting that alternative IL-4 transcript splicing may be a process shared by other simian and potentially pro-simian species as well. Extension of the study to other mammalian species led us to the assumption that generation of IL-4 splice variants may be common to primates, lagomorphs (rabbit), and rodents of the sciuridae family (woodchuck), but is unlikely to occur in mice and rats (muridae), for which IL-4 splice variants have indeed never been described. Potential implications of alternatively spliced cytokine products with possible antagonistic or competitive inhibitory function, for the choice of suitable animal models of IL-4-regulated immune processes, are discussed. This study also indicates the importance of considering alternative splicing when defining cytokine bioassays, most particularly in the present context of transcriptomics, involving the generalization of sequence-based detection methods such as quantitative reverse transcription PCR.

摘要

人类白细胞介素-4(IL-4)基因产生一种缺少外显子2的可变剪接变体,称为IL-4δ2,被描述为IL-4驱动活性的天然拮抗剂。我们报告了从黑猩猩(Pan troglodytes)骨髓样本和食蟹猴(Macaca fascicularis)活化的外周淋巴结细胞中分离出IL-4δ2 cDNA。同时首次提供了黑猩猩完整的IL-4 cDNA序列。对几种已知IL-4序列的系统发育分析表明,灵长类动物编码区结构高度保守,这表明可变的IL-4转录剪接可能也是其他猿类以及潜在的类猿物种共有的过程。将研究扩展到其他哺乳动物物种使我们推测,IL-4剪接变体的产生可能在灵长类动物、兔形目动物(兔子)和松鼠科啮齿动物(土拨鼠)中很常见,但在小鼠和大鼠(鼠科)中不太可能发生,实际上从未在小鼠和大鼠中描述过IL-4剪接变体。本文讨论了具有可能的拮抗或竞争性抑制功能的可变剪接细胞因子产物对选择合适的IL-4调节免疫过程动物模型的潜在影响。这项研究还表明,在定义细胞因子生物测定时,尤其是在当前转录组学背景下,考虑可变剪接非常重要,这涉及到基于序列的检测方法(如定量逆转录PCR)的推广。

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