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Isolation of cDNA sequences coding for a part of human tissue plasminogen activator.

机译:编码一部分人类组织纤溶酶原激活剂的cDNA序列的分离。

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摘要

We have isolated a cDNA sequence coding for a part of human tissue plasminogen activator. mRNA coding for tissue plasminogen activator was partially purified, copied into double-stranded cDNA, and cloned into Escherichia coli. Two sets of partially overlapping oligodeoxynucleotide mixtures corresponding to all possible coding sequences for a known portion of the tissue plasminogen activator gene were prepared. One set was used as a probe to screen cDNA containing bacterial clones and both were used as probes in hybridization against purified plasmid DNA. Of 4,200 bacterial clones examined, 1 carried a plasmid that hybridized to both sets of oligonucleotides. This plasmid contained a 370-base-pair cDNA insert, which was shown by nucleotide sequence analysis to code for the cleavage site region in the one-chain form of the human tissue plasminogen activator.
机译:我们已经分离出编码一部分人类组织纤溶酶原激活剂的cDNA序列。编码组织纤溶酶原激活物的mRNA被部分纯化,复制到双链cDNA中,并克隆到大肠杆菌中。制备了两组部分重叠的寡脱氧核苷酸混合物,它们对应于组织纤溶酶原激活物基因的已知部分的所有可能的编码序列。一组用作探针以筛选含有细菌克隆的cDNA,并且两者均用作与纯化质粒DNA杂交的探针。在所检查的4,200个细菌克隆中,有1个带有与两组寡核苷酸杂交的质粒。该质粒包含一个370个碱基对的cDNA插入片段,该插入片段通过核苷酸序列分析显示为编码人组织纤溶酶原激活物的单链形式的切割位点区域。

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