In order to read the information contained in DNA, first, their functional units, genes are transcribed during
transcription into
messenger ribonucleic acid (mRNA)), which is based on the complementary DNA strand. mRNA molecules serve as templates for the protein synthesis; they are transported to the
cytoplasm and repeatedly read by the
ribosomes. Before the mRNA is ready to be
translated, it undergoes several processes i.e. splicing, which means that the pre-mRNA is modified to remove certain stretches of non-coding sequences called
introns. The stretches that remain includ protein-coding sequences and are called
exons. Finally, consecutive three nucleotide bases of the mRNA sequence are translated into corresponding
amino acids and linked together to form protein chains.
Proteins are required for the structure, function, and regulation of the cells, tissues and organs. Each protein has its unique functions. The process of reading content of a gene is depicted in Figure2.
In order to understand the role and function of the genes one needs the complete information about their mRNA transcripts and proteins. Unfortunately, exploring the protein functions is very difficult due to their unique 3-dimentional complicated structure and a shortage of efficient technologies. To overcome this difficulty one may concentrate on the mRNA molecules produced by the genes of interest
(gene expression) and use this information to investigate the functional roles of the genes. This idea was a motivation for the development of microarrays technique, as a method allowing for studying the interaction between thousands of genes based on their mRNA transcript level.