5.8S ribosomal RNA

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5.8S ribosomal RNA (5.8S rRNA) is a non-coding RNA component of the large subunit of eukaryotic ribosomes. It plays a crucial role in the protein synthesis process, aiding in the assembly of the ribosome and ensuring the proper alignment of the mRNA and tRNA molecules during translation. The 5.8S rRNA is highly conserved across eukaryotes, indicating its essential function in the cell.

Structure and Function

The 5.8S rRNA is part of the ribosomal 60S subunit and is approximately 160 nucleotides in length. It is closely associated with the 28S ribosomal RNA in a region known as the sarcin-ricin loop, which is critical for the interaction with elongation factors during protein synthesis. The 5.8S rRNA forms extensive secondary and tertiary interactions with the 28S rRNA, contributing to the stability and function of the ribosome.

In addition to its structural role, 5.8S rRNA participates in the catalytic activity of the ribosome, which is termed as the ribozyme. It helps in the correct positioning of the mRNA and tRNA molecules, ensuring that amino acids are added in the correct sequence to form a protein.

Biogenesis

The biogenesis of 5.8S rRNA is a complex process that involves the transcription of a large precursor RNA molecule, known as the 45S pre-rRNA, in the nucleolus. This precursor RNA also contains the sequences for 18S and 28S rRNAs. The 45S pre-rRNA undergoes extensive modifications, including cleavage and chemical modifications, to produce the mature 18S, 5.8S, and 28S rRNAs. The 5.8S rRNA is generated through the cleavage of the ITS2 (Internal Transcribed Spacer 2) region from the pre-rRNA.

Evolutionary Significance

The high degree of conservation of 5.8S rRNA across eukaryotic species underscores its critical role in ribosome function and protein synthesis. Comparative studies of 5.8S rRNA sequences can provide insights into the evolutionary relationships among different organisms. Additionally, variations in the 5.8S rRNA sequence and structure can have implications for ribosome function and can lead to diseases.

Clinical Relevance

Alterations in the 5.8S rRNA sequence or its processing can lead to defects in ribosome assembly and function, potentially causing diseases. For example, mutations affecting ribosomal RNA processing have been linked to disorders such as Diamond-Blackfan anemia and dyskeratosis congenita. Research into the 5.8S rRNA and its interactions within the ribosome continues to be a significant area of study for understanding ribosomal pathologies and developing therapeutic strategies.

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Contributors: Prab R. Tumpati, MD