mirTarCLASH: a comprehensive miRNA target database based on chimeric read-based experiments

MicroRNAs (miRNAs) can target messenger RNAs to control their degradation or translation repression effects. Therefore, identifying the target and binding sites of different miRNAs is essential for understanding miRNA functions. To investigate these interactions, researchers have employed the cross-linking, ligation, and sequencing of hybrids (CLASH-seq) and similar CLASH-like approaches to generate chimeric reads formed by miRNAs and their targeting segments. These chimeric reads allow for the direct extraction of both the miRNA-target gene pairs and their corresponding binding sites. Nevertheless, these studies lack user-friendly platforms for researchers to investigate these interactions efficiently, thus hindering scientists' ability to explore miRNA functions. To address this gap, we developed mirTarCLASH, a comprehensive database that deposits 502 061/322 707/224 452 unique hybrid reads from human/mouse/worm miRNA chimeric read-based experiments. In mirTarCLASH, the chimera analysis algorithm ChiRA and two distinct binding site inference tools, RNAup and miRanda, were adopted to facilitate the exploration of miRNA-target pairs derived from CLASH-like experiments. Compared with existing similar repositories, mirTarCLASH further enables several confidence evaluation filters with visualization functions for the extracted results. The results can be further refined based on the key properties of the miRNA targeting sites, including read depths, numbers of supporting algorithms, and cross-linking-induced mutations, to enhance confidence levels. In addition, these miRNA-binding sites are visually represented through an integrated transcript atlas. Finally, we demonstrated the biological applicability of mirTarCLASH via the well-characterized example interaction between cel-let-7-5p and lin-41 in Caenorhabditis elegans, showcasing the potential of mirTarCLASH to provide novel insights for subsequent experimental research designs. The constructed mirTarCLASH database is freely available at https://cosbi.ee.ncku.edu.tw/MirTarClash. Database URL: https://cosbi.ee.ncku.edu.tw/MirTarClash.

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Database
Published
2025-01-01
DOI
https://doi.org/10.1093/database/baaf023
Citations
2
Primary Topic
MicroRNA in disease regulation
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article
Field-Weighted Citation Impact
1.87

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article

mirTarCLASH: a comprehensive miRNA target database based on chimeric read-based experiments

Heng-Chi Lee, Tzu-Hsien Yang, Yuan-Han Lee, Xiangwei Li et al.
2 citations
Database
MicroRNA in disease regulation
1.87
article

mirTarCLASH: a comprehensive miRNA target database based on chimeric read-based experiments

Heng-Chi Lee, Tzu-Hsien Yang, Yuan-Han Lee, Xiangwei Li, Wei-Sheng Wu, Shang-Yi Lu
article en
2 citations

Abstract

MicroRNAs (miRNAs) can target messenger RNAs to control their degradation or translation repression effects. Therefore, identifying the target and binding sites of different miRNAs is essential for understanding miRNA functions. To investigate these interactions, researchers have employed the cross-linking, ligation, and sequencing of hybrids (CLASH-seq) and similar CLASH-like approaches to generate chimeric reads formed by miRNAs and their targeting segments. These chimeric reads allow for the direct extraction of both the miRNA-target gene pairs and their corresponding binding sites. Nevertheless, these studies lack user-friendly platforms for researchers to investigate these interactions efficiently, thus hindering scientists' ability to explore miRNA functions. To address this gap, we developed mirTarCLASH, a comprehensive database that deposits 502 061/322 707/224 452 unique hybrid reads from human/mouse/worm miRNA chimeric read-based experiments. In mirTarCLASH, the chimera analysis algorithm ChiRA and two distinct binding site inference tools, RNAup and miRanda, were adopted to facilitate the exploration of miRNA-target pairs derived from CLASH-like experiments. Compared with existing similar repositories, mirTarCLASH further enables several confidence evaluation filters with visualization functions for the extracted results. The results can be further refined based on the key properties of the miRNA targeting sites, including read depths, numbers of supporting algorithms, and cross-linking-induced mutations, to enhance confidence levels. In addition, these miRNA-binding sites are visually represented through an integrated transcript atlas. Finally, we demonstrated the biological applicability of mirTarCLASH via the well-characterized example interaction between cel-let-7-5p and lin-41 in Caenorhabditis elegans, showcasing the potential of mirTarCLASH to provide novel insights for subsequent experimental research designs. The constructed mirTarCLASH database is freely available at https://cosbi.ee.ncku.edu.tw/MirTarClash. Database URL: https://cosbi.ee.ncku.edu.tw/MirTarClash.

DatabaseVol. 2025
University of Chicago (US), National Cheng Kung University (TW)
National Cheng Kung University, National Science and Technology Council, National Institutes of Health
Openalex Percentile: Top 16%
MicroRNA in disease regulation
1.87
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