Ribonuclease T1

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Ribonuclease T1 (RNase T1) is an enzyme that catalyzes the hydrolysis of RNA into smaller components. It specifically cleaves single-stranded RNA after guanine residues, thus producing oligonucleotides with 2',3'-cyclic phosphate termini. RNase T1 is widely used in molecular biology for sequence and structure studies of RNA. It is derived from the fungus Aspergillus oryzae.

Function[edit | edit source]

RNase T1 plays a crucial role in the degradation of RNA by specifically recognizing and cleaving the phosphodiester bond following a guanine nucleotide. This specificity allows for the detailed analysis of RNA sequences and the study of RNA structure and function. The enzyme's activity is essential in various biological processes, including the maturation and turnover of RNA molecules within cells.

Structure[edit | edit source]

The enzyme is a small, single-chain polypeptide that contains a high proportion of alpha-helical and beta-sheet structures, which contribute to its stability and function. The active site of RNase T1 contains residues that are critical for substrate recognition and catalysis. These include histidine, which acts as a general base in the catalytic mechanism, and glutamic acid, which helps in substrate binding.

Mechanism[edit | edit source]

RNase T1 catalyzes the cleavage of RNA via a two-step mechanism. The first step involves the enzyme binding to an RNA substrate with a guanine base exposed. The histidine residue in the active site then acts as a base to abstract a proton from the 2'-hydroxyl group of the ribose, facilitating a nucleophilic attack on the adjacent phosphodiester bond. This results in the formation of a 2',3'-cyclic phosphate intermediate. In the second step, a water molecule, activated by the enzyme, attacks the cyclic phosphate, leading to the product release with a 3'-phosphate terminus.

Applications[edit | edit source]

RNase T1 is extensively used in molecular biology and biochemistry for RNA sequencing, structure analysis, and the study of RNA-protein interactions. Its specificity for guanine allows for the precise cleavage of RNA, making it a valuable tool for mapping RNA structures and identifying functional RNA motifs within larger RNA molecules.

Clinical Significance[edit | edit source]

While RNase T1 itself is not directly involved in human disease, the study of its function and mechanism provides insights into the broader field of RNA metabolism and its implications in various diseases, including cancer and viral infections. Understanding how RNase T1 and similar enzymes interact with RNA can help in the development of therapeutic strategies targeting RNA molecules.

See Also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD