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Short Communication - (2024) Volume 10, Issue 4

Advances in Circular RNA: A New Frontier in Genomics
Aks Asliya*
 
Department of Pharmaceutics, University of Alfaisal, Saudi Arabia
 
*Correspondence: Aks Asliya, Department of Pharmaceutics, University of Alfaisal, Saudi Arabia, Email:

Received: 31-Jul-2024, Manuscript No. IPBMBJ-24-21591; Editor assigned: 02-Aug-2024, Pre QC No. IPBMBJ-24-21591 (PQ); Reviewed: 16-Aug-2024, QC No. IPBMBJ-24-21591; Revised: 21-Aug-2024, Manuscript No. IPBMBJ-24-21591 (R); Published: 28-Aug-2024, DOI: 10.36648/2471-8084-10.04.36

Introduction

In recent years, circular RNAs have emerged as a significant player in the field of genomics and molecular biology. Unlike traditional linear RNAs, circRNAs form a covalently closed loop, which makes them stable and resistant to degradation. This unique structure has spurred extensive research into their functions, mechanisms, and potential applications. Here, we explore the latest advances in circular RNA research, highlighting their biological roles, technological innovations, and future prospects. CircRNAs were first discovered in the 1970s, but their functional significance remained largely overlooked until recently. Unlike linear RNAs, which are typically transcribed from genes and then translated into proteins, circRNAs are generated through a process called back-splicing. Recent studies have elucidated several key biological functions of circRNAs. They can act as sponges for microRNAs, thereby modulating gene expression. By binding to specific miRNAs, circRNAs can prevent these small RNAs from interacting with their target mRNAs, influencing various cellular processes.

Description

Additionally, circRNAs can interact with RNA-binding proteins, affecting the stability, localization, and translation of their target mRNAs. Their involvement in regulating gene expression and cellular processes makes them crucial players in both normal physiology and disease states.

The study of circRNAs has been propelled forward by advances in sequencing technologies and bioinformatics tools. Highthroughput RNA sequencing has allowed researchers to identify and characterize circRNAs across different tissues and conditions with unprecedented precision. Innovations in sequencing methodologies, such as the use of circular RNA-specific enrichment techniques, have improved our ability to detect low-abundance circRNAs and differentiate them from linear RNAs. Bioinformatics tools and databases have also evolved to support circRNA research. Additionally, online databases like circBase and CircNet provide comprehensive resources for exploring circRNA sequences, expression profiles, and associated regulatory networks. These technological advancements have significantly enhanced our ability to study the diverse roles of circRNAs in health and disease. The functional versatility of circRNAs has led to their investigation in various diseases, including cancer, neurological disorders, and cardiovascular diseases. In cancer, for example, specific circRNAs have been identified as potential biomarkers for diagnosis and prognosis. CircRNAs can be detected in body fluids such as blood and urine, making them promising non-invasive diagnostic tools. Moreover, certain circRNAs have been found to influence cancer progression by regulating key oncogenes and tumor suppressors. In neurological disorders, circRNAs have been implicated in processes such as synaptic plasticity and neurodevelopment. Dysregulation of circRNA expression has been associated with conditions like Alzheimer’s disease and autism spectrum disorders. Understanding the role of circRNAs in these diseases could lead to novel therapeutic strategies, including the development of circRNA-based drugs or gene therapies.

The therapeutic potential of circRNAs extends beyond their role as biomarkers. Researchers are exploring strategies to manipulate circRNA levels for therapeutic purposes. For instance, artificially engineered circRNAs could be used to sequester specific miRNAs or RBPs, thereby modulating gene expression in a targeted manner. Additionally, delivery systems such as nanoparticles or viral vectors could be employed to introduce therapeutic circRNAs into cells, offering a promising avenue for gene therapy. Despite the significant progress in circRNA research, several challenges remain. One major challenge is the need for standardized methods for circRNA detection and quantification. Variability in experimental techniques and data analysis can lead to inconsistent results, making it difficult to compare findings across studies. Addressing these challenges will require collaborative efforts to establish best practices and standardized protocols [1-4].

Conclusion

Another area of interest is the functional validation of circRNAs. While many circRNAs have been identified and characterized, their precise roles and mechanisms of action are still not fully understood. Future research will need to focus on elucidating the specific functions of individual circRNAs and their interactions with other molecular players. In conclusion, the field of circular RNA research is rapidly advancing, offering new insights into gene regulation and disease mechanisms. Technological innovations and growing understanding of circRNA biology have opened up exciting possibilities for diagnostic and therapeutic applications. As research continues to evolve, circRNAs are poised to become integral components of personalized medicine and novel therapeutic strategies. The journey of circRNAs from enigmatic molecules to key players in cellular processes underscores the dynamic and ever-expanding nature of genomics.

Acknowledgement

None.

Conflict Of Interest

The author’s declared that they have no conflict of interest.

References

Citation: Asliya A (2024) Advances in Circular RNA: A New Frontier in Genomics. Biochem Mol Biol J. 10:36.

Copyright: © 2024 Asliya A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.