DHX15

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DHX15 is an enzyme that in humans is encoded by the DHX15 gene. This gene is a member of the DEAH-box family of RNA helicases, which are characterized by the conserved motif Asp-Glu-Ala-His (DEAH). DHX15 plays a significant role in RNA splicing, a critical process in the post-transcriptional modification of RNA. The enzyme is involved in the assembly of spliceosomes, complexes that are essential for the removal of introns from pre-messenger RNA (pre-mRNA). This process is vital for the generation of mature messenger RNA (mRNA), which is then translated into proteins.

Function[edit | edit source]

DHX15 is implicated in various cellular processes, primarily through its role in the regulation of RNA splicing. It participates in the spliceosome cycle, engaging in the ATP-dependent remodeling of the spliceosome complex. This activity is crucial for the fidelity and efficiency of splicing. The enzyme's function is not limited to splicing; it also has roles in mRNA export from the nucleus to the cytoplasm, ribosome biogenesis, and possibly in the innate immune response by recognizing and binding to viral RNA.

Genetic Structure[edit | edit source]

The DHX15 gene is located on chromosome 4 in humans. It consists of multiple exons that encode the DHX15 protein. The protein contains several domains characteristic of the DEAH-box family of helicases, including the ATPase domain, which is responsible for its enzymatic activity, and the helicase domain, which is involved in unwinding RNA structures.

Clinical Significance[edit | edit source]

Alterations in the DHX15 gene or its protein product have been associated with various human diseases. Mutations in DHX15 have been implicated in certain forms of cancer, suggesting a potential role in tumorigenesis. Furthermore, due to its involvement in the immune response, variations in the expression or function of DHX15 could influence susceptibility to viral infections.

Given its central role in RNA splicing and potential implications in disease, DHX15 is a subject of interest in biomedical research. Understanding the precise mechanisms by which DHX15 functions and its interactions with other cellular components may provide insights into the regulation of gene expression and the development of novel therapeutic strategies for diseases associated with splicing abnormalities.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD