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一种用于裂殖酵母粟酒裂殖酵母的拷贝数控制表达载体。

A copy-number-controlled expression vector for the fission yeast Schizosaccharomyces pombe.

作者信息

Tohda H, Okada H, Giga-Hama Y, Okayama H, Kumagai H

机构信息

Research Center, Asahi Glass Co., Ltd., Kanagawa, Japan.

出版信息

Gene. 1994 Dec 15;150(2):275-80. doi: 10.1016/0378-1119(94)90437-5.

Abstract

A novel expression vector for the fission yeast Schizosaccharomyces pombe carries the neomycin-resistance-encoding gene regulated by the SV40 early promoter, and its copy number is controlled by the level of Geneticin (G418). Foreign gene expression is driven by the human cytomegalovirus (hCMV) promoter which is transcriptionally active in S. pombe. Moreover, the vector expresses foreign genes at high levels, due to the 5'-untranslated region (5'-UTR) containing an A + T-rich sequence of about 50 nucleotides located between the TATA box of the hCMV promoter and the start codon. Recombinant human lipocortin I was produced at levels of up to 50% of the total soluble protein in the presence of 100-200 micrograms/ml of G418 in the media. Southern and Northern blotting showed that this high level of expression was due to an increase in copy number induced by G418, the high transcriptional activity of the hCMV promoter and the high translational efficiency of the 5'-UTR. We modified the vector into an 'ATG vector', named pTL2M, that maintains the 5'-UTR optimized for gene expression and into which any foreign gene, whose exact sequence is known, can be easily inserted.

摘要

一种用于粟酒裂殖酵母的新型表达载体携带由SV40早期启动子调控的新霉素抗性编码基因,其拷贝数受遗传霉素(G418)水平的控制。外源基因表达由在粟酒裂殖酵母中具有转录活性的人巨细胞病毒(hCMV)启动子驱动。此外,由于5'非翻译区(5'-UTR)在hCMV启动子的TATA盒和起始密码子之间包含一段约50个核苷酸的富含A + T的序列,该载体能够高水平表达外源基因。在培养基中存在100 - 200微克/毫升G418的情况下,重组人脂皮质素I的表达量高达总可溶性蛋白的50%。Southern和Northern印迹分析表明,这种高水平表达是由于G418诱导的拷贝数增加、hCMV启动子的高转录活性以及5'-UTR的高翻译效率。我们将该载体改造为一种“ATG载体”,命名为pTL2M,它保留了为基因表达优化的5'-UTR,并且可以轻松插入任何已知确切序列的外源基因。

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