Untranslated region
Untranslated regions (UTRs) are portions of an mRNA (messenger RNA) molecule that are not translated into protein. These regions are found at both ends of the mRNA: the 5' UTR (five prime untranslated region) is located upstream of the start codon, and the 3' UTR (three prime untranslated region) is found downstream of the stop codon. UTRs play crucial roles in the post-transcriptional regulation of gene expression, influencing mRNA stability, localization, and translation efficiency.
Function[edit | edit source]
UTRs are involved in various regulatory functions that are essential for the proper expression of genes. The 5' UTR contains elements such as the ribosome binding sites and Kozak sequence, which are critical for the initiation of translation. It can also regulate translation efficiency through secondary structures or RNA-binding protein interactions. The 3' UTR, on the other hand, contains sequences that can influence mRNA stability, polyadenylation status, and localization. It is also the site of action for microRNAs (miRNAs), small non-coding RNAs that can bind to complementary sequences in the 3' UTR, leading to mRNA degradation or inhibition of translation.
Structure[edit | edit source]
The length and sequence of UTRs can vary widely among different mRNAs. This variability allows for a diverse range of regulatory mechanisms. Secondary structures formed by UTRs, such as stem-loops, can affect their interaction with proteins and other RNAs. The presence of specific sequence motifs within UTRs can also dictate their binding affinity for regulatory molecules.
Clinical Significance[edit | edit source]
Alterations in UTR sequences or in the regulatory mechanisms involving UTRs can lead to diseases. Mutations in the UTRs can disrupt normal gene expression by affecting mRNA stability, localization, or translation. For example, mutations in the 5' UTR of the Ferritin gene can lead to hereditary hyperferritinemia-cataract syndrome, while mutations in the 3' UTR of some genes have been linked to various cancers due to the deregulation of gene expression.
Research[edit | edit source]
Research on UTRs is ongoing, with studies focusing on understanding the complex regulatory networks involving UTRs and their potential therapeutic applications. For instance, targeting the interactions between miRNAs and 3' UTRs is being explored as a strategy for cancer therapy.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD