Hogarth P M, Witort E, Hulett M D, Bonnerot C, Even J, Fridman W H, McKenzie I F
Research Centre for Cancer and Transplantation, University of Melbourne, Parkville, Australia.
J Immunol. 1991 Jan 1;146(1):369-76.
We have isolated and deduced the structure of the beta Fc gamma RII gene from the mouse. This gene spans approximately 18 kb of DNA; the structure and nucleotide sequence has been determined and potential regulatory sites identified. This gene is composed of 10 exons that give rise to the beta 1 and beta 2 Fc gamma RII cDNA. Four exons encode the 5' untranslated region and leader sequence, one exon for each Ig-binding domain and membrane-spanning region and three exons encoding the cytoplasmic tail and 3' untranslated region. Analysis of the gene structure indicated that the beta 1Fc gamma RII and beta 2Fc gamma RII arise by differential mRNA splicing when a single 141-bp exon (exon 8) is alternately spliced to give rise to these isoforms. Sequence analysis of 2 kbp upstream of the transcription start site indicated the presence of regulatory elements, including three binding sites for the transcription factor Sp1, and Ap-4 binding site, a tandem glucocorticoid response element, and an overlapping tandem repeat. Furthermore, as in the Thy-1 gene, no CAT or TATA consensus sequences were observed. In addition, sites of methylation that regulate expression of this gene were also located at the 5' end of the gene and within several introns. A large intron located between exons 4 and 5 also contained a series of purine/pyrimidine-rich regions and a potential enhancer sequence.
我们从小鼠中分离并推导了β FcγRII基因的结构。该基因跨越约18kb的DNA;已确定其结构和核苷酸序列,并鉴定了潜在的调控位点。该基因由10个外显子组成,可产生β1和β2 FcγRII cDNA。四个外显子编码5'非翻译区和前导序列,每个Ig结合域和跨膜区各有一个外显子,三个外显子编码胞质尾和3'非翻译区。基因结构分析表明,当一个141bp的外显子(外显子8)交替剪接产生这些异构体时,β1FcγRII和β2FcγRII通过差异mRNA剪接产生。转录起始位点上游2kbp的序列分析表明存在调控元件,包括转录因子Sp1的三个结合位点、一个Ap-4结合位点、一个串联糖皮质激素反应元件和一个重叠串联重复序列。此外,与Thy-1基因一样,未观察到CAT或TATA共有序列。另外,调节该基因表达的甲基化位点也位于基因的5'端和几个内含子内。位于外显子4和5之间的一个大内含子也包含一系列富含嘌呤/嘧啶的区域和一个潜在的增强子序列。