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鸡干扰素调节因子-2(IRF-2)cDNA的克隆:IRF-2基因的表达与定位

Cloning of chicken interferon regulatory factor-2 (IRF-2) cDNA: expression and mapping of the IRF-2 gene.

作者信息

Marienfeld R, Nanda I, Zöller B, Schmid M, Rebbert M, Jungwirth C

机构信息

Institute for Virology and Immunobiology, University of Würzburg, Germany.

出版信息

J Interferon Cytokine Res. 1997 Apr;17(4):219-27. doi: 10.1089/jir.1997.17.219.

Abstract

A cDNA clone encoding a member of the avian interferon regulatory factor (IRF) family homologous to mammalian IRF-2 was isolated from cDNA library from poly[rI:rC]-induced chicken embryo fibroblasts (CEF). The deduced amino acid sequence shows a characteristic DNA binding domain of 124 amino acids at the amino-terminal end with 96.8% identity to human and 96% to mouse IRF-2. Identities in the C-terminal part are 77.5% and 77%, respectively. Identity to all other known members of the chicken IRF (Ch-IRF) family is distinctly lower. In C32 cells, an IRF-2 mRNA of 2.4 kb is constitutively expressed in very low amounts but is inducible by Ch-IFN in the absence or presence of cycloheximide. The Ch-IRF-2 gene is a single copy gene and was mapped by fluorescence in situ hybridization to the long arm of chromosome 4.

摘要

从经聚肌苷酸

聚胞苷酸(poly[rI:rC])诱导的鸡胚成纤维细胞(CEF)的cDNA文库中分离出一个编码与哺乳动物IRF-2同源的禽干扰素调节因子(IRF)家族成员的cDNA克隆。推导的氨基酸序列在氨基末端显示出一个由124个氨基酸组成的特征性DNA结合结构域,与人类IRF-2的同一性为96.8%,与小鼠IRF-2的同一性为96%。在羧基末端部分的同一性分别为77.5%和77%。与鸡IRF(Ch-IRF)家族的所有其他已知成员的同一性明显较低。在C32细胞中,2.4 kb的IRF-2 mRNA以非常低的量组成性表达,但在不存在或存在环己酰亚胺的情况下可被Ch-IFN诱导。Ch-IRF-2基因是一个单拷贝基因,通过荧光原位杂交定位到4号染色体的长臂上。

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