MicroArray and Gene Expression

From WikiMD's Food, Medicine & Wellness Encyclopedia

Microarray technology is a powerful laboratory tool used to study gene expression across thousands of genes simultaneously. This technology has revolutionized the field of genomics, enabling researchers to understand complex genetic interactions and the molecular basis of diseases at an unprecedented scale.

Overview[edit | edit source]

A microarray consists of a small, solid support, typically a glass slide, onto which DNA sequences are fixed in an orderly manner at specific locations called spots. Each spot contains picomoles of a specific DNA sequence, known as probes. These probes can hybridize to complementary DNA or RNA in a sample, allowing for the detection of gene expression levels of thousands of genes in a single experiment.

Types of Microarrays[edit | edit source]

There are several types of microarrays, including DNA microarrays, RNA microarrays (also known as expression microarrays), and protein microarrays. DNA microarrays are used for genome mapping, mutation analysis, and gene identification. RNA microarrays are used primarily to measure the expression levels of genes across different conditions or treatments. Protein microarrays, while less common, are used to study protein interactions and activities.

Applications[edit | edit source]

Microarray technology has a wide range of applications in biomedical research, diagnostics, and drug discovery. It is used to identify gene expression patterns in cancer, infectious diseases, and genetic disorders, which can lead to the development of new diagnostic tests and targeted therapies. Microarrays are also used in the study of genotype-phenotype correlations, epigenetics, and comparative genomic hybridization.

Procedure[edit | edit source]

The microarray procedure involves several steps: 1. Sample Preparation: RNA or DNA is extracted from the sample and labeled with fluorescent dyes. 2. Hybridization: The labeled samples are then hybridized to the microarray slide. 3. Washing: After hybridization, the slide is washed to remove non-specifically bound material. 4. Scanning: The microarray is scanned to detect the fluorescent signals, which indicate the presence and quantity of the target nucleic acid. 5. Data Analysis: The intensity of the fluorescence signals is analyzed to determine the expression levels of the genes.

Challenges and Limitations[edit | edit source]

Despite its many advantages, microarray technology has limitations. The quality of the data can be affected by variations in the hybridization process, cross-hybridization, and signal detection. Additionally, microarrays can only detect sequences that have been included on the array, limiting their ability to discover new genes or variants.

Future Directions[edit | edit source]

With the advent of next-generation sequencing (NGS) technologies, the use of microarrays has declined in some areas. However, microarrays still offer a cost-effective option for certain applications, such as genotyping and expression profiling on a large scale. Ongoing advancements in microarray technology, including higher density arrays and improved data analysis methods, continue to expand its utility in research and clinical settings.


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Contributors: Prab R. Tumpati, MD