bioRxiv Science⌕ Search

Biology subjects

Rizvi, A. Z.

Publications and source records attributed to Rizvi, A. Z..

3 recordsLinked to original sources

PLncFire: A Scalable Pipeline for Transcriptome-wide Discovery of Plant lncRNAs

BackgroundLong non-coding RNAs (lncRNAs) play important regulatory roles in plant growth, development, and stress responses. However, their genome-wide identification remains challenging due to low sequence conservation, incomplete reference annotations, and variability across species. Existing workflows often lack standardization and reproducibility, limiting large-scale comparative studies. To address these challenges, we developed PLncFire, a modular computational pipeline designed for automated and reproducible identification and annotation of plant lncRNAs using RNA-seq data. MethodsPLncFire processes standard RNA-seq datasets through a structured workflow comprising quality control, read alignment, transcript assembly, and transcript filtering. A consensus-based coding potential assessment strategy was implemented using CPC2, PlantLncPipe, and FEELnc to improve prediction reliability. Transcripts were filtered based on length, exon structure, and coding probability thresholds to generate high-confidence lncRNA candidates. Identified lncRNAs were further classified as known or novel by comparison with reference annotations. The pipeline also incorporates differential expression analysis to support functional prioritization. Workflow modularity ensures scalability across plant species and enables reproducible execution in diverse computational environments. ResultsApplication of PLncFire to plant RNA-seq datasets enabled systematic identification of high-confidence lncRNA candidates, including both previously annotated and novel transcripts. The consensus coding-potential framework reduced false-positive predictions compared to single-tool approaches. Integration of differential expression analysis facilitated prioritization of lncRNAs associated with specific developmental stages or stress conditions. The modular design demonstrated compatibility across datasets from different plant species, supporting cross-species adaptability and comparative analysis. ConclusionsPLncFire provides a standardized and reproducible framework for genome-wide lncRNA discovery in plants. By integrating multi-tool consensus coding assessment with transcript assembly and expression analysis, the pipeline enhances prediction confidence and scalability. This platform supports large-scale functional genomics studies and facilitates systematic exploration of plant lncRNA landscapes. The source code is available at https://github.com/ahsan-rizvi/PLncFire.git. Trial registrationNot applicable.

bioinformatics↗

Computational mapping of the differentially expressed gene-lncRNA pairs present at the root nodule developmental stages of Arachis hypogaea

RNA-sequencing (RNA-seq) data analysis of the different stages of root nodules formation in peanut Arachis hypogaea investigate the genetic features. Genes related to the root nodules formations in this plant are extensively studied [1] [2] [3] [4] [5], but less information is present for their relations with long noncoding RNAs (lncRNAs). Bioinformatics techniques are utilised here to identify the novel lncRNAs present in the publically available RNA-seq data reported [6] for the different stages of root nodules formation in this plant. Highly correlated, significant, and Differentially Expressed (DE) gene-lncRNA pairs are also detected to understand the epigenetic control of lncRNA. These pairs are further differentiated between cis and trans antisense lncRNAs and lincRNAs based on their functions and positions from the genes. Obtained results are the catalogue for the highly correlated and significant DE gene-lncRNA pairs related to root nodules formation in A. hypogaea.

bioinformatics↗

Transcriptomic analyses with the progress of symbiosis in ‘crack-entry’ legume Arachis hypogaea highlight its contrast with ‘Infection thread’ adapted legumes

In root-nodule symbiosis, rhizobial invasion and nodule organogenesis is host controlled. In most legumes, rhizobia enter through infection-threads and nodule primordium in the cortex is induced from a distance. But in dalbergoid legumes like Arachis hypogaea, rhizobia directly invade cortical cells through epidermal cracks to generate the primordia. Herein we report the transcriptional dynamics with the progress of symbiosis in A. hypogaea at 1dpi: invasion; 4dpi: nodule primordia; 8dpi: spread of infection in nodule-like structure; 12dpi: immature nodules containing rod-shaped rhizobia; and 21dpi: mature nodules with spherical symbiosomes. Expression of putative orthologue of symbiotic genes in crack-entry legume A. hypogaea was compared with infection thread adapted model legumes. The contrasting features were (i) higher expression of receptors like LYR3, EPR3 as compared to canonical NFRs (ii) late induction of transcription factors like NIN, NSP2 and constitutive high expression of ERF1, EIN2, bHLH476 and (iii) induction of divergent pathogenesis responsive PR-1 genes. Additionally, symbiotic orthologues of SymCRK, FLOT4, ROP6, RR9, NOOT and SEN1 were not detectable and microsynteny analysis indicated the absence of RPG and DNF2 homologues in diploid parental genomes of A. hypogaea. The implications are discussed and a molecular framework that guide crack-entry symbiosis in A. hypogaea is proposed.

plant biology↗