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使用碘化单链M13探针促进快速DNA序列分析——小鼠赖氨酸tRNA基因的核苷酸序列

Using iodinated single-stranded M13 probes to facilitate rapid DNA sequence analysis--nucleotide sequence of a mouse lysine tRNA gene.

作者信息

Han J H, Harding J D

出版信息

Nucleic Acids Res. 1983 Apr 11;11(7):2053-64. doi: 10.1093/nar/11.7.2053.

Abstract

From a recombinant lambda phage, we have determined a 387 bp sequence containing a mouse lysine tRNA gene. The putative lys tRNA (anticodon UUU) differs from rabbit liver lys tRNA at five positions. The flanking regions of the mouse gene are not generally homologous to published human and Drosophila lys tRNA genes. However, the mouse gene contains a 14 bp region comprising 13 A-T base pairs, 30-44 bp from the 5' end of the coding region. Cognate A-T rich regions are present in human and Drosophila genes. The coding region is flanked by two 11 bp direct repeats, similar to those associated with alu family sequences. The sequence was determined by a "walking" protocol that employs, as a novel feature, iodinated single-stranded M13 probes to identify M13 subclones which contain sequences partially overlapping and contiguous to an initially determined sequence. The probes can also be used to screen lambda phage and in Southern and dot blot experiments.

摘要

从一个重组λ噬菌体中,我们确定了一段包含小鼠赖氨酸tRNA基因的387 bp序列。推测的赖氨酸tRNA(反密码子UUU)在五个位置上与兔肝赖氨酸tRNA不同。小鼠基因的侧翼区域通常与已发表的人类和果蝇赖氨酸tRNA基因不同源。然而,小鼠基因包含一个14 bp的区域,由13个A-T碱基对组成,位于编码区5'端30 - 44 bp处。人类和果蝇基因中也存在同源的富含A-T的区域。编码区两侧有两个11 bp的直接重复序列,类似于与alu家族序列相关的那些序列。该序列是通过一种“步移”方案确定的,该方案采用碘化单链M13探针作为新特征来识别包含与最初确定序列部分重叠且相邻的序列的M13亚克隆。这些探针还可用于筛选λ噬菌体以及进行Southern杂交和斑点杂交实验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7021/325861/ea03e197cd28/nar00352-0110-a.jpg

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