Literature DB >> 24121022

Revealing natural antisense transcripts from Plasmodium vivax isolates: evidence of genome regulation in complicated malaria.

P A Boopathi1, Amit Kumar Subudhi, Shilpi Garg, Sheetal Middha, Jyoti Acharya, Deepak Pakalapati, Vishal Saxena, Mohammed Aiyaz, Bipin Chand, Raja C Mugasimangalam, Sanjay K Kochar, Parmendra Sirohi, Dhanpat K Kochar, Ashis Das.   

Abstract

Plasmodium vivax is the most geographically widespread human malaria parasite causing approximately 130-435 million infections annually. It is an economic burden in many parts of the world and poses a public health challenge along with the other Plasmodium sp. The biology of this parasite is less studied and poorly understood, in spite of these facts. Emerging evidence of severe complications due to infections by this parasite provides an impetus to focus research on the same. Investigating the parasite directly from infected patients is the best way to study its biology and pathogenic mechanisms. Gene expression studies of this parasite directly obtained from the patients has provided evidence of gene regulation resulting in varying amount of transcript levels in the different blood stages. The mechanisms regulating gene expression in malaria parasites are not well understood. Discovery of Natural Antisense Transcripts (NATs) in Plasmodium falciparum has suggested that these might play an important role in regulating gene expression. We report here the genome-wide occurrence of NATs in P. vivax parasites from patients with differing clinical symptoms. A total of 1348 NATs against annotated gene loci have been detected using a custom designed microarray with strand specific probes. Majority of NATs identified from this study shows positive correlation with the expression pattern of the sense (S) transcript. Our data also shows condition specific expression patterns of varying S and antisense (AS) transcript levels. Genes with AS transcripts enrich to various biological processes. To our knowledge this is the first report on the presence of NATs from P. vivax obtained from infected patients with different disease complications. The data suggests differential regulation of gene expression in diverse clinical conditions, as shown by differing sense/antisense ratios and would lead to future detailed investigations of gene regulation.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Keywords:  1,3 BPG; 1,3-biphosphoglycerate; 2-Oxaloglutarate; 2-phophoglycerate; 2OG; 2PG; 3-phosphoglycerate; 3PG; 6-phophogluconate; 6-phosphoglucono-δ-lactone, 6PGNT, 6-phophogluconate; 6PGNL; 6PGNT; AC-COA; ACON-C; ASP; CIT; Complicated malaria; DHAP; DR1P; DR5P; E4P; F-6-P; F6P; FBP; FUM; G-6-P; G3P; GAP; GDP-4-oxo-6-deoxy-mannose; GDP-FUC; GDP-Fucose; GDP-L-fucose synthetase; GDP-MAN; GDP-Mannose; GDP-ODM; GLC; GLCN6P; GLCNAC1P; GLCNAC6P; GLN; GLU; GLYC; GLYC3P; ICT; Isocitrate; LAC; MAL; MAN; MAN1P; MAN6P; N-acetyl-glucosamime-6-phosphate; N-acetyl-glucosamine-1-phosphate; Natural antisense transcripts; OXA; PEP; PVX_001945; PVX_080515; PVX_091100; PVX_094915; PVX_099535; PVX_111455; PVX_118255; PVX_118495; PYR; Plasmodium vivax; R5P; RU5P; S7P; SUC; SUC-COA; Strand specific microarray; UDP-GLCNAC; UDP-N-acetyl-glucosamine. Gene coding for protein:PVX_114315, hexokinase, putative; Uncomplicated malaria; X5P; acetyl-CoA; aspartate; cis-aconitate; citrate; deoxyribose-1-phosphate; deoxyribose-5-phosphate; deoxyribose-phosphate aldolase; dihydroxy-acetone-phosphate; erythrose-4-phosphate; fructose 1,6-bis phosphate; fructose 1,6-bisphosphate aldolase; fructose-6-phosphate; fumarate; glucosamine-6-phosphate; glucosamine-fructose-6-phosphate aminotransferase; glucose; glucose-6-phosphate; glutamate; glutamine; glyceraldehyde 3-phosphate; glyceraldehyde-3-phophate; glycerol; glycerol-3-phosphate; lactate; malate; mannose; mannose-1-phosphate; mannose-6-phosphate; oxaloacetate; phosphoenolpyruvate; phosphoglycerate kinase; pyruvate; ribose 5-phosphate epimerase; ribose-5-phosphate; ribulose-5-phosphate; sedoheptulose-7-phosphate, F6P, fructose-6-phosphate; succinate; succinyl-COA; succinyl-CoA synthetase alpha subunit; triosephosphate isomerase; xylulose-5-phosphate, G3P, glyceraldehyde-3-phophate

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Year:  2013        PMID: 24121022     DOI: 10.1016/j.meegid.2013.09.026

Source DB:  PubMed          Journal:  Infect Genet Evol        ISSN: 1567-1348            Impact factor:   3.342


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3.  Dataset of natural antisense transcripts in P. vivax clinical isolates derived using custom designed strand-specific microarray.

Authors:  P A Boopathi; Amit Kumar Subudhi; Shilpi Garg; Sheetal Middha; Jyoti Acharya; Deepak Pakalapati; Vishal Saxena; Mohammed Aiyaz; Bipin Chand; Raja C Mugasimangalam; Sanjay K Kochar; Parmendra Sirohi; Dhanpat K Kochar; Ashis Das
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Review 6.  Plasmodium vivax Biology: Insights Provided by Genomics, Transcriptomics and Proteomics.

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