ISSN: 2167-7948
+44 1300 500008
Commentary Article - (2024)Volume 13, Issue 2
The multidisciplinary science of bioinformatics, which uses computational tools to evaluate biological data, has become important in comprehending intricate biological processes, such as the functioning of hormones. Thyroxine (T4) and Triiodothyronine (T3) are the two main thyroid hormones, and they are essential for controlling growth, development and metabolism in a variety of tissues. Using bioinformatics techniques to identify and clarify the roles of thyroid hormones in various organs provides profound understanding of the hormones' many physiological functions as well as the underlying molecular processes. This paper examines the many bioinformatics approaches used to study the activities of thyroid hormone in different tissues.
Understanding thyroid hormone functions
Thyroid hormones control the expression of genes, which affects a broad range of physiological functions. Thyroid Hormone Receptors (TRs), which are nuclear receptors functioning as transcription factors, bind to T3, the active form of thyroid hormone. The expression of target genes involved in metabolism, development and differentiation is subsequently regulated by these TRs. Bioinformatics techniques are essential to map thyroid hormone actions across many tissues because of the systemic nature of their activity.
Transcriptomics and gene expression analysis
An important bioinformatics method for comprehending thyroid hormone actions is transcriptomics, which is the study of all RNA transcripts generated by the genome. The investigation of gene expression patterns in response to thyroid hormones in various organs may be done in-depth thanks to RNA sequencing (RNA-Seq) technology. Gene expression levels in thyroid hormone-treated vs untreated samples are compared using differential gene expression analysis. DESeq2 and EdgeR are two popular bioinformatics tools used for this purpose. Researchers can deduce the pathways and processes affected by thyroid hormones in certain tissues by identifying genes whose expression is markedly changed by these hormones. Thyroid hormones, for instance, may upregulate genes related to lipid metabolism and down regulate those linked to inflammation in the liver. Genes that exhibit differential expression can be categorized into molecular activities, biological processes, and cellular components using Gene Ontology (GO) and pathway enrichment analysis. Gene Set Enrichment Analysis (GSEA) and DAVID are well-known utilities. The influence of thyroid hormones on cellular processes in different tissues is better understood thanks to these investigations. To illustrate the significance of thyroid hormones in energy metabolism, GO analysis may show, for example, that they increase mitochondrial activity in muscle tissues.
Epigenomics and chromatin accessibility
The field of epigenomics is concerned with the analysis of variations in gene expression brought about by processes other than sequence variations in the DNA, such as histone modifications and DNA methylation. Assays such as ATAC-Seq (Assay for Transposase-Accessible Chromatin utilizing sequencing) can be used to study chromatin accessibility, which is a measure of chromatin's openness to transcription factors and can be affected by thyroid hormones. Thyroid hormone receptorbound DNA regions can be identified using chromatin immuno precipitation sequencing (ChIP-Seq). Researchers can precipitate DNA-protein complexes and sequence the corresponding DNA by using antibodies that are specific to TRs. Using bioinformatics methods like as MACS (Model-based Analysis of ChIP-Seq), peaks representing TR binding sites are found in the sequencing data. This methodology facilitates the mapping of thyroid hormone-influenced regulatory areas across diverse tissues, offering valuable insights into the regulation of genes particular to each tissue. Thyroid hormone regulation of gene expression may be fully understood by combining transcriptomic (such as RNA-Seq) and epigenomic (such as ChIP-Seq, ATACSeq) data. By using integrative analytic techniques like as Cistrome-GO, researchers may establish a connection between alterations in gene expression and TR binding sites, which in turn reveals the regulatory networks that are influenced by thyroid hormones in different tissues.
Proteomics and protein interaction networks
Proteomics the large-scale study of proteins, including their structures and functions, is essential for understanding the downstream effects of thyroid hormone action. Thyroid hormone-influenced post-translational changes may be identified and protein quantities can be measured with the use of Mass Spectrometry (MS). Protein abundance in thyroid hormone-treated vs untreated samples is determined by analyzing MS data using bioinformatics tools such as Proteome Discoverer and MaxQuant. This method sheds light on the roles of tissue-specific proteins by identifying those whose levels are controlled by thyroid hormones. Protein-Protein Interaction (PPI) networks show how different proteins interact with one another inside a cell. These interactions can be modulated by thyroid hormones, which can impact different signaling pathways. PPI networks are built and shown using bioinformatics tools such as STRING and Cytoscape. Researchers can determine important proteins and pathways controlled by thyroid hormones in various tissues by combining proteomics data with PPI networks.
Citation: Nai V (2024) Bioinformatics Approaches for Recognizing Thyroid Hormone Function in Various Tissues. Thyroid Disorders Ther. 13:333.
Received: 27-May-2024, Manuscript No. JTDT-24-32006; Editor assigned: 30-May-2024, Pre QC No. JTDT-24-32006 (PQ); Reviewed: 14-Jun-2024, QC No. JTDT-24-32006; Revised: 21-Jun-2024, Manuscript No. JTDT-24-32006 (R); Published: 28-Jun-2024 , DOI: 10.35841/2167-7948.24.13.333
Copyright: © 2024 Nai V. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.