The FREM1 protein, encoded by the FRAS1-related extracellular matrix 1 gene, plays a significant role in the structural composition of the extracellular matrix and is crucial for maintaining tissue integrity. This protein is intricately involved in embryonic development, with a particular focus on the formation of a stable basement membrane, which is necessary for the proper development of epithelial structures. Mutations within the FREM1 gene have been linked to developmental disorders, which highlights the importance of its expression in normal physiological processes. Given the integral part FREM1 plays in development, understanding the regulation of its expression is essential for gaining insights into the complex orchestration of cellular and molecular events during tissue formation.
Research into the regulation of gene expression has identified a variety of chemical compounds that can potentially act as activators for genes like FREM1. For instance, compounds such as retinoic acid and all-trans retinal are known to engage with retinoid receptors, which can trigger a cascade of transcriptional events culminating in the upregulation of developmental genes. Similarly, molecules such as vitamin D3, through its active form, interact with specific receptors that can stimulate the transcription of genes associated with cellular differentiation and proliferation. Other compounds like β-estradiol and hydrocortisone are involved in the body's hormonal signaling pathways and can initiate transcriptional activities that potentially elevate the expression of genes integral to tissue health and stability. Moreover, agents such as sodium butyrate and forskolin can alter chromatin accessibility or increase messenger signals within cells, respectively, leading to a rise in the transcription of certain genes. Curcumin and resveratrol, on the other hand, are known to activate transcription factors and signaling pathways, potentially resulting in the induction of gene expression. Each of these compounds engages with unique cellular mechanisms, suggesting a diverse array of interactions that can lead to the increased expression of proteins like FREM1, which are key to maintaining the architecture and function of various tissues.
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