Drosha

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5b16_drosha_dgcr8.png

Drosha is a ribonuclease enzyme that is crucial in the microRNA (miRNA) processing pathway. It is a member of the RNase III family and is encoded by the DROSHA gene in humans. Drosha is primarily involved in the initial step of miRNA biogenesis, where it cleaves primary miRNA (pri-miRNA) transcripts into precursor miRNA (pre-miRNA) in the cell nucleus.

Function[edit | edit source]

Drosha functions as part of a larger complex known as the Microprocessor complex, which also includes the protein DGCR8 (DiGeorge syndrome critical region gene 8). The primary role of Drosha within this complex is to recognize and cleave pri-miRNA substrates, producing a characteristic ~70 nucleotide stem-loop structure known as pre-miRNA. This pre-miRNA is then exported to the cytoplasm by the Exportin-5 protein, where it undergoes further processing by another RNase III enzyme, Dicer, to generate mature miRNA.

Structure[edit | edit source]

Drosha is a large protein composed of multiple domains, including two RNase III domains and a double-stranded RNA-binding domain (dsRBD). The RNase III domains are responsible for the catalytic activity of the enzyme, while the dsRBD aids in substrate recognition and binding. The precise coordination of these domains is essential for the accurate and efficient processing of pri-miRNA substrates.

Role in Disease[edit | edit source]

Mutations or dysregulation of Drosha can lead to various diseases, including certain types of cancer. For example, altered Drosha expression has been observed in breast cancer, lung cancer, and other malignancies. The disruption of normal miRNA processing due to defective Drosha activity can result in aberrant gene expression, contributing to tumorigenesis and cancer progression.

Research and Therapeutic Potential[edit | edit source]

Given its central role in miRNA biogenesis, Drosha is a target of interest in the development of therapeutic strategies for diseases associated with miRNA dysregulation. Researchers are exploring ways to modulate Drosha activity to restore normal miRNA processing in disease states. Additionally, understanding the detailed mechanisms of Drosha function and regulation can provide insights into the broader aspects of RNA biology and gene regulation.

See also[edit | edit source]

References[edit | edit source]

External links[edit | edit source]


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Contributors: Prab R. Tumpati, MD