Tone Y, Thompson S A, Babik J M, Nolan K F, Tone M, Raven C, Waldmann H
Sir William Dunn School of Pathology, University of Oxford, GB.
Eur J Immunol. 1996 Jun;26(6):1222-7. doi: 10.1002/eji.1830260606.
Interleukin-12 (IL-12) is a heterodimeric cytokine composed of p35 and p40 subunits and is required for induction of T helper 1 (Th1) responses. Knowledge of how the IL-12 gene is regulated will permit an understanding of susceptibility and resistance to pathogenic microbes and to autoiummune diseases. In this report, we provide the gene structures, nucleotide sequences and chromosomal assignment for the p35 and p40 subunits of mouse IL-12. The p35 and p40 subunit genes are distributed over 8 kb and 14 kb, and map to chromosomes 3 and 11, respectively. The p35 subunit gene consists of eight exons, including a 5'-noncoding exon that was defined by sequence comparison of genomic DNA with the 5'ends of novel cDNA molecules. Transcription of p35 mRNA can start from the first exon but can also initiate further downstream. Potential transcription regulatory elements, AP1, AP2, AP3, NF-kB and GATA recognition sequences, are located within 523 bp upstream of the p35 gene; however, no TATA box was identified. The p40 subunit gene consists of eight exons. A TATA box is located 30 bp upstream from the transcription start site, and AP1, AP3, GATA, and Pu.1 recognition sequences are located within 690 bp upstream of the p40 gene. An AGTTTCTACTTT sequence, which acts as an interferon-gamma response element in the promoter of the major histocompatibility complex class I gene, was also found upstream of the p40 gene.
白细胞介素-12(IL-12)是一种由p35和p40亚基组成的异源二聚体细胞因子,是诱导辅助性T细胞1(Th1)反应所必需的。了解IL-12基因如何被调控将有助于理解对致病微生物和自身免疫性疾病的易感性和抗性。在本报告中,我们提供了小鼠IL-12的p35和p40亚基的基因结构、核苷酸序列和染色体定位。p35和p40亚基基因分别分布在8 kb和14 kb区域,分别定位于3号和11号染色体。p35亚基基因由八个外显子组成,包括一个5'-非编码外显子,该外显子是通过基因组DNA与新cDNA分子5'端的序列比较确定的。p35 mRNA的转录可以从第一个外显子开始,但也可以在更下游起始。潜在的转录调控元件,AP1、AP2、AP3、NF-κB和GATA识别序列,位于p35基因上游523 bp内;然而,未发现TATA盒。p40亚基基因由八个外显子组成。一个TATA盒位于转录起始位点上游30 bp处,AP1、AP3、GATA和Pu.1识别序列位于p40基因上游690 bp内。在p40基因上游还发现了一个AGTTTCTACTTT序列,该序列在主要组织相容性复合体I类基因启动子中作为干扰素-γ反应元件起作用。