Introduction Functional genomics has been defined as the use of molecular biological tools to explore gene function and interaction in genomic sequencing data (SERC, 2013). Expressed sequence tags (ESTs) and gene expression series analysis (SAGE) are among the techniques commonly used in functional genomics. The goal of transcriptome research is to identify transcripts expressed in the genome. Since the human genome research, EST is the major technology used for transcript identification. Recently SAGE has been widely used for transcriptome analysis.
In order to understand the control of gene expression, it is necessary to understand two important concepts. Firstly, gene expression requires a process to prepare transcription, ie messenger ribonucleic acid (mRNA) copies of the deoxyribonucleic acid (DNA) gene. Transcription can only be done when RNA polymerase first adheres to or binds to DNA. Controlling this binding process is a major means of regulating gene expression and protein is the main regulator of binding. The second important concept is that protein molecules that help regulate binding can themselves be regulated. This usually occurs when other molecules are bound to proteins and the structure of the protein changes, ie the shape changes. In some cases, this shape change will aid RNA polymerase binding to DNA, in other cases it will prevent polymerization of DNA.
Gene expression is the process by which genetic instructions are used to produce gene products such as proteins. Our gene has a protein blueprint. Once a particular gene is expressed, the protein will be produced in the cell in which it is expressed. The difference between different types of cells is due to the different expressed proteins. To test gene expression, the Cambridge University team collected blood and tissue samples from 16,000 people in the northern hemisphere and the southern hemisphere. Several factors were measured, including the type and amount of cells in the blood, and the protein composition of the cells in blood and tissues. In various countries such as Gambia and the UK, several cells and proteins show consistent seasonal variation in different populations.
Live cells are the product of a gene expression program that involves regulated transcription of thousands of genes. The gene expression program relies on the recognition of specific promoter sequences by transcription regulatory proteins. How the panels of regulatory proteins are related to genes in the genome can be explained as transcription regulatory networks. We have determined how most transcriptional regulators encoded by eukaryotic S. cerevisiae are related to genes in the genome of living cells. Just as metabolic network maps explain the potential pathways that cells can use to complete a metabolic process, this map of transcriptional regulatory networks is based on the fact that yeast cells regulate a comprehensive gene expression program Explain latent paths that can be used for. We describe eukaryotic network motifs and use networks that regulate gene interactions to show how they can be incorporated into functional modules.