Full length cDNA homogenizing subtractive hybridization method

Abstract

The invention provides a method for homogenization subtractive hybridization of full length cDNA. The method comprises the following steps in sequence: (1) synthesizing a first chain cDNA; (2) synthesizing a double chain cDNA; (3) selective connection and primer extension; (4) subtractive hybridization; (5) PCR augmentation of cDNA of differential expression; wherein, the PCR products of the subtractive hybridization can be directly cloned to a vector so as to construct cDNA libraries, where differentially expressed genes are concentrated; the libraries can be utilized to analyze gene expression, prepare gene chips and be marked as probe which selects the differentially expressed genes from the existing libraries; in addition, if the subtractive efficiency is not high enough, the subtractive hybridization can repeat for the PCR products of subtractive hybridization to improve the homogenization and the subtractive efficiency. The method for homogenization subtractive hybridization of the full length cDNA (FNSH) creates the beneficial effects of high subtractive efficiency of differential genes, high efficiency of enriching differential expressed genes, high homogenization and gainof the full length cDNA.

Description

A full-length cDNA homogeneous subtractive hybridization method (1) Technical field The invention relates to a full-length cDNA normalized subtractive hybridization (full-lengthnormalizationsubtractivehybridization, FNSH) method, which is applied to enrichment, screening, cloning and identification of differentially expressed genes. (2) Background technology The types and quantities of genes expressed by various tissues or cells of an organism, and the same tissue or cell at different developmental stages are not the same, and these genes with different expression levels or expression stages are called differentially expressed genes. . Differentially expressed genes play an important role in the development, differentiation, and carcinogenesis of organisms, so cloning and identification of these differentially expressed genes can strongly promote our research and reveal the mechanism of these life processes. At present, the methods for screening differentially expressed g...

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Problems solved by technology

The above-mentioned methods have a common shortcoming: that is, what is obtained is a partial fragment of cDNA; to obtain a full-length cDNA sequence, it is necessary to use rapid amplification of cDNA ends (rapid amplification of cDNA ends, RACE) or screen from a cDNA library, but there is a selective Promoter, cleavage and polyadenylation signal sequences, and when the gene belongs to a multigene family, it will be very difficult to obtain a correct full-length cDNA sequence with RACE, and the construction of cDNA library and screening itself are time-consuming strenuous work

In addition, the above methods also have some other disadvantages: DD can only obtain partial cDNA sequences of a few genes at a time, which cannot be applied to high-throughput screening, and has a high false positive rate; RDA cannot effectively extract non-target molecules. If it is subtracted, the false positive rate is also higher, and it is more conducive to the enrichment of genes with high expression levels, and it is easy to lose the information of genes with low expression levels; SAGE requires a large number of sequencing and analysis of a large amount of sequence information, and the cost is high; SSH Although it is efficient and can uniformize the content of cDNA with different expression levels, there are also certain false positives, and the strength of inhibitory PCR is controlled by many factors, which greatly affects the results. In addition, the double-stranded driver in SSH makes subtractive hybridization Efficiency cannot be further improved

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