Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7002
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dc.contributor.authorDAVE, BRUHADen_US
dc.contributor.authorKANYAL, ABHISHEKen_US
dc.contributor.authorMAMATHARANI, D. V.en_US
dc.contributor.authorKARMODIYA, KRISHANPALen_US
dc.date.accessioned2022-05-31T08:23:01Z
dc.date.available2022-05-31T08:23:01Z
dc.date.issued2022-06en_US
dc.identifier.citationNAR Genomics and Bioinformatics, 4(2), lqac036.en_US
dc.identifier.issn2631-9268en_US
dc.identifier.urihttps://doi.org/10.1093/nargab/lqac036en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7002
dc.description.abstractSingle-nucleotide variations (SNVs) in RNA, arising from co- and post-transcriptional phenomena including transcription errors and RNA-editing, are well studied in a range of organisms. In the malaria parasite Plasmodium falciparum, stage-specific and non-specific gene-expression variations accompany the parasite's array of developmental and morphological phenotypes over the course of its complex life cycle. However, the extent, rate and effect of sequence-level variation in the parasite's transcriptome are unknown. Here, we report the presence of pervasive, non-specific SNVs in the P. falciparum transcriptome. SNV rates for a gene were correlated to gene length (r≈0.65–0.7) but not to the AT-content of that gene. Global SNV rates for the P. falciparum lines we used, and for publicly available P. vivax and P. falciparum clinical isolate datasets, were of the order of 10–3 per base, ∼10× higher than rates we calculated for bacterial datasets. These variations may reflect an intrinsic transcriptional error rate in the parasite, and RNA editing may be responsible for a subset of them. This seemingly characteristic property of the parasite may have implications for clinical outcomes and the basic biology and evolution of P. falciparum and parasite biology more broadly. We anticipate that our study will prompt further investigations into the exact sources, consequences and possible adaptive roles of these SNVs.en_US
dc.language.isoenen_US
dc.publisherOxford University Pressen_US
dc.subjectBiologyen_US
dc.subject2022-MAY-WEEK3en_US
dc.subjectTOC-MAY-2022en_US
dc.subject2022en_US
dc.titlePervasive sequence-level variation in the transcriptome of Plasmodium falciparumen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleNAR Genomics and Bioinformaticsen_US
dc.publication.originofpublisherForeignen_US
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