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编码鸡前清蛋白一部分的双链cDNA的克隆。从部分纯化的mRNA中分离特定DNA序列的通用方法。

Cloning of a double-stranded cDNA that codes for a portion of chicken preproalbumin. A general method for isolating a specific DNA sequence from partially purified mRNA.

作者信息

Gordon J I, Burns A T, Christmann J L, Deeley R G

出版信息

J Biol Chem. 1978 Dec 10;253(23):8629-39.

PMID:711769
Abstract

A scheme is presented for cloning a double-stranded cDNA molecule that codes for a portion of chicken preproalbumin. This method, which does not require pure mRNA or cDNA, has widespread applicability. Chicken preproalbumin was identified as a Mr = 72,000 polypeptide by immunoprecipitation of proteins synehesized in a wheat germ cell-free translation system from total, guanidine.HCl-extracted, rooster liver RNA. After removal of the bulk of the ribosomal RNA by poly(U)-Sephadex G-10 chromatography, albumin mRNA was enriched approximately 2-fold by centrifugation through low salt, isokinetic sucrose gradients, until it represented about 30% of the mRNA sequences present. Double-stranded cDNA prepared from this mRNA was then inserted into the Pst 1 site of the plasmid PBR322 by the "G-C tailing" technique and the recombinant DNA was used to transform Echerichia coli stran X1776. Transformants containing putative albumin DNA sequences were identified by colony hybridization with a cDNA probe that was highly enriched for albumin cDNA sequences. This probe was isolated by hybridizing the partially purified RNA preparation to its cDNA, under conditions of RNA excess, to a R0t value such that only the most abundant cDNA sequences had hybridized. Unhybridized, less abundant, sequences were destroyed by subsequent S1 nuclease digestion. The identity of clones that hybridized to this abundant class cDNA was established by DNA-mRNA hybrid-arrested cell-free translation. Hybridization of nick-translated, albumin-containing, plasmid DNA to total liver poly(A)+ RNA, that had been separated on methyl mercury agarose gels and transferred to diazobenzyloxymethyl paper, established that avian albumin mRNA has a molecular weight of 850,000. This molecular weight corresponds to approximately 2,600 nucleotides, or 600 nucleotides longer than the size required to code for the preproalbumin polypeptide.

摘要

本文介绍了一种克隆编码鸡前白蛋白原部分序列的双链cDNA分子的方法。该方法无需纯mRNA或cDNA,具有广泛的适用性。通过对用盐酸胍从公鸡肝脏总RNA中提取的蛋白质在麦胚无细胞翻译系统中合成的蛋白质进行免疫沉淀,将鸡前白蛋白原鉴定为一种分子量为72,000的多肽。通过聚(U)-葡聚糖凝胶G-10柱层析去除大部分核糖体RNA后,通过低盐等密度蔗糖梯度离心使白蛋白mRNA富集约2倍,直至其占存在的mRNA序列的约30%。然后,用“G-C加尾”技术将从该mRNA制备的双链cDNA插入质粒pBR322的Pst I位点,并将重组DNA用于转化大肠杆菌菌株X1776。通过与高度富集白蛋白cDNA序列的cDNA探针进行菌落杂交,鉴定出含有假定白蛋白DNA序列的转化体。该探针是通过在RNA过量的条件下,将部分纯化的RNA制剂与其cDNA杂交至R0t值,使得只有最丰富的cDNA序列杂交而分离得到的。未杂交的、较不丰富的序列通过随后的S1核酸酶消化被破坏。通过DNA-mRNA杂交抑制的无细胞翻译确定与这种丰富类cDNA杂交的克隆的身份。将经切口平移的含白蛋白的质粒DNA与在甲基汞琼脂糖凝胶上分离并转移至重氮苄氧基甲基纸上的肝脏总poly(A)+RNA杂交,确定禽白蛋白mRNA的分子量为850,000。该分子量对应于约2600个核苷酸,比编码前白蛋白原多肽所需的大小长600个核苷酸。

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