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小鼠2-5A合成酶基因座:来自两个连锁基因的三种不同转录本。

The murine 2-5A synthetase locus: three distinct transcripts from two linked genes.

作者信息

Rutherford M N, Kumar A, Nissim A, Chebath J, Williams B R

机构信息

Research Institute, Hospital for Sick Children, Toronto, Canada.

出版信息

Nucleic Acids Res. 1991 Apr 25;19(8):1917-24. doi: 10.1093/nar/19.8.1917.

Abstract

The cloning of cDNAs encoding murine 2-5A synthetase has identified three related transcripts, represented by a previously described cDNA clone, L3 and two novel cDNAs, L1 and L2. L1 contains an open reading frame coding for a protein that shows 70% conservation at the amino acid level when compared to the protein predicted to be encoded by L3. L2 recognizes an IFN-induced transcript 600-bp larger than the L3 transcript. These three cDNAs map to a cosmid, cII, containing two murine 2-5A synthetase genes, ME12 and ME5/ME8, situated in a head-to-tail orientation separated by approximately 8 kb. Southern analyses of ME12 and ME5/ME8 using L3, L1-specific and L2-specific probes indicate that these genes have a similar organization. cII was transiently and stably transfected into CV-1 cells. When treated with interferon, the transfected cells produced mature, murine 2-5A synthetase transcripts identified using L3 and L2-specific probes. Thus all transcripts present in IFN-treated mouse cells which are recognized by the available murine 2-5A synthetase cDNA probes map to an approximately 40 kb region of the mouse genome containing two 2-5A synthetase genes.

摘要

编码小鼠2-5A合成酶的cDNA克隆已鉴定出三种相关转录本,分别由先前描述的cDNA克隆L3以及两个新的cDNA L1和L2代表。L1包含一个开放阅读框,编码一种蛋白质,与预计由L3编码的蛋白质相比,该蛋白质在氨基酸水平上具有70%的保守性。L2识别一种干扰素诱导的转录本,比L3转录本大600个碱基对。这三个cDNA定位于一个粘粒cII,该粘粒包含两个小鼠2-5A合成酶基因ME12和ME5/ME8,它们以头对尾的方向排列,相隔约8 kb。使用L3、L1特异性和L2特异性探针对ME12和ME5/ME8进行Southern分析表明,这些基因具有相似的组织结构。cII被瞬时和稳定地转染到CV-1细胞中。用干扰素处理时,转染细胞产生了使用L3和L2特异性探针鉴定的成熟小鼠2-5A合成酶转录本。因此,干扰素处理的小鼠细胞中所有能被现有小鼠2-5A合成酶cDNA探针识别的转录本都定位于小鼠基因组中一个约40 kb的区域,该区域包含两个2-5A合成酶基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495f/328124/0e32208d4928/nar00088-0178-a.jpg

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