Saunders M E, Gewert D R, Tugwell M E, McMahon M, Williams B R
EMBO J. 1985 Jul;4(7):1761-8. doi: 10.1002/j.1460-2075.1985.tb03848.x.
The enzyme 2-5A synthetase is induced in cultured cells in response to interferon (IFN) treatment. A lambda gt10 cDNA library of mRNA from IFN-induced Daudi lymphoblastoid cells was screened with oligonucleotide probes. Several overlapping cDNAs were isolated and shown to be derived from the human synthetase gene using filter selection and oocyte microinjection assays. The nucleotide sequence of one of these, cDNA 8-2, extended the 2-5A synthetase sequence already described 72 bp in the 5' direction but was found to differ significantly in coding sequence at the 3' end. The longest cDNA isolated (6-2) was approximately 1.4 kb. By Northern hybridization analysis single mRNAs of 1.7 kb were detected in Daudi and T98G (glioblastoma) cells. However, in HeLa cells, four mRNAs ranging in size from 1.5 to 3.5 kb were found, one of which differed at the 3' end. Analysis of both phage and cosmid genomic clones and comparison with genomic DNA indicate that there is a single gene for 2-5A synthetase, comprising at least six exons and five introns, which can undergo a novel form of alternative RNA processing depending on cell type.
2-5A合成酶在培养细胞中经干扰素(IFN)处理后被诱导产生。用寡核苷酸探针筛选来自IFN诱导的Daudi淋巴母细胞样细胞的mRNA的λgt10 cDNA文库。通过滤膜选择和卵母细胞显微注射分析,分离出几个重叠的cDNA,并证明它们源自人类合成酶基因。其中一个cDNA 8-2的核苷酸序列在5'方向上延伸了已描述的2-5A合成酶序列72 bp,但发现在3'端的编码序列有显著差异。分离出的最长cDNA(6-2)约为1.4 kb。通过Northern杂交分析,在Daudi和T98G(胶质母细胞瘤)细胞中检测到1.7 kb的单一mRNA。然而,在HeLa细胞中,发现了四种大小从1.5到3.5 kb不等的mRNA,其中一种在3'端有所不同。对噬菌体和黏粒基因组克隆的分析以及与基因组DNA的比较表明,2-5A合成酶有一个单一基因,至少由六个外显子和五个内含子组成,根据细胞类型可进行一种新型的可变RNA加工。