首页> 外文期刊>Nucleic Acids Research >DESCRIPTION OF THE ENTIRE MRNA POPULATION BY A 3' END CDNA FRAGMENT GENERATED BY CLASS IIS RESTRICTION ENZYMES
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DESCRIPTION OF THE ENTIRE MRNA POPULATION BY A 3' END CDNA FRAGMENT GENERATED BY CLASS IIS RESTRICTION ENZYMES

机译:类IIS限制酶产生的3'端CDNA片段对整个MRNA种群的描述

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摘要

A novel means of recording the expression status of the total gene population is described, Digestion of cDNA by class IIS restriction enzymes produces a fragment with a poly (A) stretch and a 5' overhang with an unknown sequence, This fragment contains information such as the class IIS enzyme that cuts cDNA nearest to the poly (A) stretch, the sequence of the 5' overhang, and the size of the fragment. Expressed genes can be discriminated and displayed by the fragment as follows: (i) cut the cDNA with one class IIS restriction enzyme; (ii) ligate the digested cDNA to that from a pool of 64 biotinylated adaptors cohesive to all possible overhangs; (iii) digest by other two class IIS enzymes; (iv) recover the ligated molecules with streptavidin-coated paramagnetic beads; (v) perform PCR with the adaptor-primer and an anchored oligo-dT primer; (vi) separate the amplified fragments by denaturing polyacrylamide gel electrophoresis. Repeat the experiment with 64 adaptors, three enzymes and three anchored oligo-dT primers displays most of the expressed genes, Because redundancy is minimized, this technique is also ideal for generating tags for expressed genes, with which to construct a transcript map of the genome.
机译:描述了一种记录总基因群体表达状态的新方法,通过IIS类限制酶消化cDNA可产生一个片段,该片段带有一个poly(A)延伸片段和一个5'突出端,具有未知序列,该片段包含诸如以下信息IIS类酶,可将最接近poly(A)片段的cDNA切开,5'突出端的序列以及片段的大小。表达的基因可以通过该片段区分和展示,如下所示:(i)用一类IIS限制酶切割cDNA; (ii)将消化的cDNA与64个生物素化的衔接子连接起来,这些衔接子对所有可能的突出端均具有粘性; (iii)用另外两种IIS酶消化; (iv)用链霉亲和素包被的顺磁珠回收连接的分子; (v)用衔接子引物和锚定的oligo-dT引物进行PCR; (vi)通过变性聚丙烯酰胺凝胶电泳分离扩增的片段。使用64个衔接子,三种酶和三种锚定的oligo-dT引物重复该实验,可显示大多数表达的基因。由于冗余度最小,因此该技术也是生成表达基因的标签的理想方法,可用于构建基因组的转录图。

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