Dataset Information

MRNALocater: Enhance the prediction accuracy of eukaryotic mRNA subcellular localization by using model fusion strategy.

ABSTRACT: The functions of mRNAs are closely correlated with their locations in cells. Knowledge about the subcellular locations of mRNA is helpful to understand their biological functions. In recent years, it has become a hot topic to develop effective computational models to predict eukaryotic mRNA subcellular localizations. However, existing state-of-the-art models still have certain deficiencies in terms of prediction accuracy and generalization ability. Therefore, it is urgent to develop novel methods to accurately predict mRNA subcellular localizations. In this study, a novel method called mRNALocater was proposed to detect the subcellular localization of eukaryotic mRNA by adopting the model fusion strategy. To fully extract information from mRNA sequences, the electron-ion interaction pseudopotential and pseudo k-tuple nucleotide composition were used to encode the sequences. Moreover, the correlation coefficient filtering algorithm and feature forward search technology were used to mine hidden feature information, which guarantees that mRNALocater can be more effectively applied to new sequences. The results based on the independent dataset tests demonstrate that mRNALocater yields promising performances for predicting eukaryotic mRNA subcellular localizations and is a powerful tool in practical applications. A freely available online web server for mRNALocater has been established at http://bio-bigdata.cn/mRNALocater.

SUBMITTER: Tang Q

PROVIDER: S-EPMC8353198 | biostudies-literature | 2021 Aug

REPOSITORIES: biostudies-literature

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Publications

mRNALocater: Enhance the prediction accuracy of eukaryotic mRNA subcellular localization by using model fusion strategy.

Tang Qiang Q Nie Fulei F Kang Juanjuan J Chen Wei W

Molecular therapy : the journal of the American Society of Gene Therapy 20210403 8

The functions of mRNAs are closely correlated with their locations in cells. Knowledge about the subcellular locations of mRNA is helpful to understand their biological functions. In recent years, it has become a hot topic to develop effective computational models to predict eukaryotic mRNA subcellular localizations. However, existing state-of-the-art models still have certain deficiencies in terms of prediction accuracy and generalization ability. Therefore, it is urgent to develop novel method ...[more]

PMID: 33823302

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Project description:BackgroundThe subcellular localization of mRNA plays a crucial role in gene expression regulation and various cellular processes. However, existing wet lab techniques like RNA-FISH are usually time-consuming, labor-intensive, and limited to specific tissue types. Researchers have developed several computational methods to predict mRNA subcellular localization to address this. These methods face the problem of class imbalance in multi-label classification, causing models to favor majority classes and overlook minority classes during training. Additionally, traditional feature extraction methods have high computational costs, incomplete features, and may lead to the loss of critical information. On the other hand, deep learning methods face challenges related to hardware performance and training time when handling complex sequences. They may suffer from the curse of dimensionality and overfitting problems. Therefore, there is an urgent need for more efficient and accurate prediction models.ResultsTo address these issues, we propose a multi-label classifier, EDCLoc, for predicting mRNA subcellular localization. EDCLoc reduces training pressure through a stepwise pooling strategy and applies grouped convolution blocks of varying sizes at different levels, combined with residual connections, to achieve efficient feature extraction and gradient propagation. The model employs global max pooling at the end to further reduce feature dimensions and highlight key features. To tackle class imbalance, we improved the focal loss function to enhance the model's focus on minority classes. Evaluation results show that EDCLoc outperforms existing methods in most subcellular regions. Additionally, the position weight matrix extracted by multi-scale CNN filters can match known RNA-binding protein motifs, demonstrating EDCLoc's effectiveness in capturing key sequence features.ConclusionsEDCLoc outperforms existing prediction tools in most subcellular regions and effectively mitigates class imbalance issues in multi-label classification. These advantages make EDCLoc a reliable choice for multi-label mRNA subcellular localization. The dataset and source code used in this study are available at https://github.com/DellCode233/EDCLoc .

Project description:BackgroundThe expansion of raw protein sequence databases in the post genomic era and availability of fresh annotated sequences for major localizations particularly motivated us to introduce a new improved version of our previously forged eukaryotic subcellular localizations prediction method namely "ESLpred". Since, subcellular localization of a protein offers essential clues about its functioning, hence, availability of localization predictor would definitely aid and expedite the protein deciphering studies. However, robustness of a predictor is highly dependent on the superiority of dataset and extracted protein attributes; hence, it becomes imperative to improve the performance of presently available method using latest dataset and crucial input features.ResultsHere, we describe augmentation in the prediction performance obtained for our most popular ESLpred method using new crucial features as an input to Support Vector Machine (SVM). In addition, recently available, highly non-redundant dataset encompassing three kingdoms specific protein sequence sets; 1198 fungi sequences, 2597 from animal and 491 plant sequences were also included in the present study. First, using the evolutionary information in the form of profile composition along with whole and N-terminal sequence composition as an input feature vector of 440 dimensions, overall accuracies of 72.7, 75.8 and 74.5% were achieved respectively after five-fold cross-validation. Further, enhancement in performance was observed when similarity search based results were coupled with whole and N-terminal sequence composition along with profile composition by yielding overall accuracies of 75.9, 80.8, 76.6% respectively; best accuracies reported till date on the same datasets.ConclusionThese results provide confidence about the reliability and accurate prediction of SVM modules generated in the present study using sequence and profile compositions along with similarity search based results. The presently developed modules are implemented as web server "ESLpred2" available at http://www.imtech.res.in/raghava/eslpred2/.

Project description:BackgroundThe computational prediction of mycobacterial proteins' subcellular localization is of key importance for proteome annotation and for the identification of new drug targets and vaccine candidates. Several subcellular localization classifiers have been developed over the past few years, which have comprised both general localization and feature-based classifiers. Here, we have validated the ability of different bioinformatics approaches, through the use of SignalP 2.0, TatP 1.0, LipoP 1.0, Phobius, PA-SUB 2.5, PSORTb v.2.0.4 and Gpos-PLoc, to predict secreted bacterial proteins. These computational tools were compared in terms of sensitivity, specificity and Matthew's correlation coefficient (MCC) using a set of mycobacterial proteins having less than 40% identity, none of which are included in the training data sets of the validated tools and whose subcellular localization have been experimentally confirmed. These proteins belong to the TBpred training data set, a computational tool specifically designed to predict mycobacterial proteins.ResultsA final validation set of 272 mycobacterial proteins was obtained from the initial set of 852 mycobacterial proteins. According to the results of the validation metrics, all tools presented specificity above 0.90, while dispersion sensitivity and MCC values were above 0.22. PA-SUB 2.5 presented the highest values; however, these results might be biased due to the methodology used by this tool. PSORTb v.2.0.4 left 56 proteins out of the classification, while Gpos-PLoc left just one protein out.ConclusionBoth subcellular localization approaches had high predictive specificity and high recognition of true negatives for the tested data set. Among those tools whose predictions are not based on homology searches against SWISS-PROT, Gpos-PLoc was the general localization tool with the best predictive performance, while SignalP 2.0 was the best tool among the ones using a feature-based approach. Even though PA-SUB 2.5 presented the highest metrics, it should be taken into account that this tool was trained using all proteins reported in SWISS-PROT, which includes the protein set tested in this study, either as a BLAST search or as a training model.

Dataset Information

MRNALocater: Enhance the prediction accuracy of eukaryotic mRNA subcellular localization by using model fusion strategy.

Publications

mRNALocater: Enhance the prediction accuracy of eukaryotic mRNA subcellular localization by using model fusion strategy.

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