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噬菌体0X174 DNA复制起点附近一个长度为71个碱基对的DNA片段的核苷酸序列。

The nucleotide sequence of a DNA fragment, 71 base pairs in length, near the origin of DNA replication of bacteriophage 0X174.

作者信息

Mansfeld A D, Vereijken J M, Jansz H S

出版信息

Nucleic Acids Res. 1976 Oct;3(10):2827-44. doi: 10.1093/nar/3.10.2827.

Abstract

Part of the nucleotide sequence of a restriction fragment covering the origin of phiX174 DNA replication 1 has been determined. The fragment A7c was obtained by digestion of phiX174 RF DNA by the restriction enzyme from Arthrobacter luteus, Alu 1. It was further cleaved into two fragments, one large and one small, by the action of the restriction enzyme from Haemophilus aegyptius, Hae 111. The nucleotide sequence of the small fragment has been determined by analysis of the transcription products obtained by the action of Escherichia coli DNA-dependent RNA polymerase on denaturated template under conditions of low salt. Transcripts longer than the template were found. The whole sequence of 71 nucleotide pairs could be derived from complementary oligonucleotides, obtained after digestion of the transcripts with T1 or pancreatic RNAase. The sequence suggests that at least 4 of the 5 amber mutants 2 that have been mapped on this fragment are identical. On account of this and other evidence a reading frame is proposed.

摘要

已确定了覆盖φX174 DNA复制起点1的一个限制片段的部分核苷酸序列。片段A7c是通过用来自藤黄节杆菌的限制酶Alu 1消化φX174 RF DNA获得的。它通过来自埃及嗜血杆菌的限制酶Hae III的作用进一步切割成两个片段,一个大的和一个小的。小片段的核苷酸序列已通过分析在低盐条件下大肠杆菌DNA依赖性RNA聚合酶作用于变性模板所获得的转录产物来确定。发现了比模板长的转录本。71个核苷酸对的完整序列可以从用T1或胰RNA酶消化转录本后获得的互补寡核苷酸推导出来。该序列表明,已定位在该片段上的5个琥珀突变体2中至少有4个是相同的。基于此及其他证据,提出了一个阅读框。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1efd/343130/46db5af814b0/nar00495-0423-a.jpg

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