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Analysis of Single-cell Gene Transcription by RNA Fluorescent In Situ Hybridization (FISH)
Published on: October 7, 2012
Directional gene expression and antisense transcripts in sexual and asexual stages of Plasmodium falciparum
María J López-Barragán1, Jacob Lemieux, Mariam Quiñones
1Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, Maryland 20892, USA.
Background:
It has been shown that nearly a quarter of the initial predicted gene models in the Plasmodium falciparum genome contain errors. Although there have been efforts to obtain complete cDNA sequences to correct the errors, the coverage of cDNA sequences on the predicted genes is still incomplete, and many gene models for those expressed in sexual or mosquito stages have not been validated. Antisense transcripts have widely been reported in P. falciparum; however, the extent and pattern of antisense transcripts in different developmental stages remain largely unknown.
Results:
We have sequenced seven bidirectional libraries from ring, early and late trophozoite, schizont, gametocyte II, gametocyte V, and ookinete, and four strand-specific libraries from late trophozoite, schizont, gametocyte II, and gametocyte V of the 3D7 parasites. Alignment of the cDNA sequences to the 3D7 reference genome revealed stage-specific antisense transcripts and novel intron-exon splicing junctions. Sequencing of strand-specific cDNA libraries suggested that more genes are expressed in one direction in gametocyte than in schizont. Alternatively spliced genes, antisense transcripts, and stage-specific expressed genes were also characterized.
Conclusions:
It is necessary to continue to sequence cDNA from different developmental stages, particularly those of non-erythrocytic stages. The presence of antisense transcripts in some gametocyte and ookinete genes suggests that these antisense RNA may play an important role in gene expression regulation and parasite development. Future gene expression studies should make use of directional cDNA libraries. Antisense transcripts may partly explain the observed discrepancy between levels of mRNA and protein expression.
Insights
This study reveals stage-specific antisense transcripts in Plasmodium falciparum, highlighting their potential role in gene regulation and parasite development. Further sequencing is crucial for understanding non-erythrocytic stage gene expression.
Area of Science:
- Genomics
- Parasitology
- Molecular Biology
Background:
- Significant errors exist in predicted Plasmodium falciparum gene models.
- Incomplete cDNA coverage hinders validation, especially for sexual and mosquito stages.
- The role and patterns of antisense transcripts across P. falciparum developmental stages are largely unknown.
Purpose of the Study:
- To investigate stage-specific gene expression and antisense transcripts in Plasmodium falciparum.
- To identify novel splicing junctions and characterize gene expression patterns.
- To provide insights into gene regulation and parasite development.
Main Methods:
- Sequencing of bidirectional and strand-specific cDNA libraries from various Plasmodium falciparum developmental stages (ring, trophozoite, schizont, gametocyte, ookinete).
- Alignment of cDNA sequences to the 3D7 reference genome.
- Characterization of alternatively spliced genes and antisense transcripts.
Main Results:
- Discovery of stage-specific antisense transcripts and novel intron-exon splicing junctions.
- Observation that gametocytes exhibit more unidirectional gene expression compared to schizonts.
- Identification of alternatively spliced genes, antisense transcripts, and stage-specific expressed genes.
Conclusions:
- Continued cDNA sequencing across diverse developmental stages, especially non-erythrocytic ones, is essential.
- Antisense transcripts in gametocyte and ookinete genes may regulate gene expression and parasite development.
- Directional cDNA libraries are recommended for future studies; antisense transcripts may explain mRNA-protein expression discrepancies.
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