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人类甘氨酸转运RNA(反密码子GCC)的核苷酸序列。

The nucleotide sequence of human tRNAGly (anticodon GCC).

作者信息

Gupta R C, Roe B A, Randerath K

出版信息

Nucleic Acids Res. 1979 Oct 25;7(4):959-70. doi: 10.1093/nar/7.4.959.

Abstract

The sequence of tRNAGCCGly from human placenta was determined by recently developed postlabeling techniques. The tRNA was digested completely with RNases T1 and A in the presence of alkaline phosphatase, the oligonucleotides were 3'-terminally (3H)-labeled, mapped on PEI-cellulose thin layers, isolated, and sequenced by methods based on base-specific cleavages. Overlaps were obtained by readout sequencing techniques on polyacrylamide gels and PEI-cellulose thin layers. The thin-layer readout technique was used also to locate and identify modified nucleotides. The primary structure was found to exhibit a large degree of homology (94.6%) with silkworm tRNAGCCGly but only 67.6% homology with human tRNACCCGly.

摘要

通过最近开发的后标记技术确定了来自人胎盘的tRNAGCCGly的序列。在碱性磷酸酶存在的情况下,用核糖核酸酶T1和A将tRNA完全消化,对寡核苷酸进行3'-末端(3H)标记,在聚乙烯亚胺纤维素薄层上进行图谱分析,分离并通过基于碱基特异性切割的方法进行测序。通过在聚丙烯酰胺凝胶和聚乙烯亚胺纤维素薄层上的读出测序技术获得重叠序列。薄层读出技术也用于定位和鉴定修饰核苷酸。发现其一级结构与家蚕tRNAGCCGly具有高度同源性(94.6%),但与人tRNACCCGly的同源性仅为67.6%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa82/342274/b311ab0a8545/nar00457-0144-a.jpg

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