Analysis of gene family expression

Abstract

The present invention relates to methods and compositions for characterizing the expression patterns of genes and gene families. Specifically, the present invention provides means to generate and monitor gene expression profiles resulting from cellular and physiological changes such that the expression patterns of individual genes or groups of genes can be readily identified and characterized.

Description

[0001] The present invention relates to methods and compositions for characterizing the expression patterns of genes and gene families. Specifically, the present invention provides means to generate and monitor gene expression profiles resulting from cellular and physiological changes such that the expression patterns of individual genes or groups of genes can be readily identified and characterized.[0002] Developing methods to detect molecular alterations in biological samples is key to increasing our knowledge about the causes of diseases, the processes of cellular development and differentiation, and other physiological and cellular events, and in developing tools to detect, treat, alter, and monitor these conditions. Perhaps the most significant alteration that can occur in a cell is in its pattern of gene transcription, which exerts profound control on protein levels and activities. Thus, the detection of changes in mRNA levels in the thousands of genes expressed by a single ce...

AI Technical Summary

Benefits of technology

[0085] The present invention relates to methods and compositions for characterizing the expression patterns of genes and gene families. Specifically, the present invention provides means to generate and monitor gene expression profiles resulting from cellular and physiological changes such that the expression patterns of individual genes or groups of genes can be readily identified and characterized. Importantly, it provides a novel technology that eliminates the cumbersome cloning and sequencing strategies required by the previously developed methods of characterizing gene expression.

[0086] Methods of the presently claimed invention, called RAGE (Restriction Analysis of Gene Expression), provide superior means to characterize the gene expression patterns of cells and tissues, identify changes in gene expession responsible for various physiological, developmental, and disease states, and identify and characterize factors that alter gene expression (e.g., drugs). RAGE involves generating or obtaining cDNA from a desired sample, PCR amplifying the cDNA with a degenerate primer set based on conserved motifs of a gene family (e.g., protein families), purifying amplified PCR products that meet appropriate criteria, and, optionally, digesting the purified products with an appropriate set of restriction endonucleases to produce an expression profile. The profile provides expression data for all members of the targeted gene family, including genes that have not been previously identified (i.e., the RAGE method provides a means of identifying new members of gene families). Expression profiles from different samples can be compared (e.g., cancer and non-cancer) to identify differentially expressed genes, to identify a sample as being of a specific type (i.e., comparing the sample to known profiles representing the various potential physiological states of the sample), and to determine the effects of factors (e.g., drugs) on the expression of genes or groups of genes, among other applications. Because of the ease of use, accuracy, sensitivity, and reproducibility of the RAGE method, this technique will find great value in detecting and characterizing molecular alterations in biological samples.

[0088] The RAGE method overcomes many of the shortcomings of the previously developed means of characterizing gene expression and maintains many of their advantages. The RAGE method utilizes a PCR amplification step and can be applied to smaller amounts of starting material than non-PCR based technologies. However, unlike the other PCR-based technologies, RAGE does not require cloning and sequencing of amplified products. Like SAGE and EST sequencing, the RAGE method allows an immediate, unambiguous identification of signals produced by known genes as well as the discovery and measurement of previously unknown genes, but does not require labor-intensive, time-consuming sequencing, and provides the ability to analyze specific gene families rather than all expressed genes. Unlike RAGE, the signals produced by differential displays cannot be quickly assigned to specific genes and, of course, the signals in hybridization based methods are limited to the known sequences the investigator has placed in the array. Like microarray hybridization methods, RAGE allows the parallel processing of a larger number of samples simultaneously. In contrast to the microarray methods, RAGE does not require a significant investment in the generation of a new array each time a new samples are to be tested. Additionally, the RAGE method is scaleable according to the needs and resources of the particular researchers using it. RAGE can be done in any laboratory with a the capability to perform PCR. It is also possible for the method to be utilized on multiple automated devices dedicated to a project attempting to measure the expression levels of thousands of genes in hundreds of samples.

Problems solved by technology

Unlike RAGE, the signals produced by differential displays cannot be quickly assigned to specific genes and, of course, the signals in hybridization based methods are limited to the known sequences the investigator has placed in the array.

Images