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      BJLD-CMI: a predictive circRNA-miRNA interactions model combining multi-angle feature information

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          Abstract

          Increasing research findings suggest that circular RNA (circRNA) exerts a crucial function in the pathogenesis of complex human diseases by binding to miRNA. Identifying their potential interactions is of paramount importance for the diagnosis and treatment of diseases. However, long cycles, small scales, and time-consuming processes characterize previous biological wet experiments. Consequently, the use of an efficient computational model to forecast the interactions between circRNA and miRNA is gradually becoming mainstream. In this study, we present a new prediction model named BJLD-CMI. The model extracts circRNA sequence features and miRNA sequence features by applying Jaccard and Bert’s method and organically integrates them to obtain CMI attribute features, and then uses the graph embedding method Line to extract CMI behavioral features based on the known circRNA-miRNA correlation graph information. And then we predict the potential circRNA-miRNA interactions by fusing the multi-angle feature information such as attribute and behavior through Autoencoder in Autoencoder Networks. BJLD-CMI attained 94.95% and 90.69% of the area under the ROC curve on the CMI-9589 and CMI-9905 datasets. When compared with existing models, the results indicate that BJLD-CMI exhibits the best overall competence. During the case study experiment, we conducted a PubMed literature search to confirm that out of the top 10 predicted CMIs, seven pairs did indeed exist. These results suggest that BJLD-CMI is an effective method for predicting interactions between circRNAs and miRNAs. It provides a valuable candidate for biological wet experiments and can reduce the burden of researchers.

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              Circular RNAs are a large class of animal RNAs with regulatory potency.

              Circular RNAs (circRNAs) in animals are an enigmatic class of RNA with unknown function. To explore circRNAs systematically, we sequenced and computationally analysed human, mouse and nematode RNA. We detected thousands of well-expressed, stable circRNAs, often showing tissue/developmental-stage-specific expression. Sequence analysis indicated important regulatory functions for circRNAs. We found that a human circRNA, antisense to the cerebellar degeneration-related protein 1 transcript (CDR1as), is densely bound by microRNA (miRNA) effector complexes and harbours 63 conserved binding sites for the ancient miRNA miR-7. Further analyses indicated that CDR1as functions to bind miR-7 in neuronal tissues. Human CDR1as expression in zebrafish impaired midbrain development, similar to knocking down miR-7, suggesting that CDR1as is a miRNA antagonist with a miRNA-binding capacity ten times higher than any other known transcript. Together, our data provide evidence that circRNAs form a large class of post-transcriptional regulators. Numerous circRNAs form by head-to-tail splicing of exons, suggesting previously unrecognized regulatory potential of coding sequences.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2683105/overviewRole: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1721228/overviewRole: Role:
                URI : https://loop.frontiersin.org/people/1640730/overviewRole: Role:
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                URI : https://loop.frontiersin.org/people/2539976/overviewRole:
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                10 May 2024
                2024
                : 15
                : 1399810
                Affiliations
                [1] 1 School of information Engineering , Xijing University , Xi’an, China
                [2] 2 College of Grassland and Environment Sciences , Xinjiang Agricultural University , Ürümqi, China
                Author notes

                Edited by: Chunhou Zheng, Anhui University, China

                Reviewed by: Jin-Xing Liu, University of Health and Rehabilitation Sciences, China

                Yijie Ding, University of Electronic Science and Technology of China, China

                *Correspondence: Chang-Qing Yu, xaycq@ 123456163.com ; Li-Ping Li, cs2bioinformatics@ 123456gmail.com
                Article
                1399810
                10.3389/fgene.2024.1399810
                11116695
                4dfa6769-b251-4754-93bd-e7532ac22046
                Copyright © 2024 Zhao, Yu, Li, Wang, Song and Wei.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 13 March 2024
                : 03 April 2024
                Funding
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by the National Natural Science Foundation of China under Grant Nos 62273284, 62172338, and 62072378.
                Categories
                Genetics
                Original Research
                Custom metadata
                Computational Genomics

                Genetics
                circrna-mirna interaction,circrna,mirna,graph embedding,autoencoder
                Genetics
                circrna-mirna interaction, circrna, mirna, graph embedding, autoencoder

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