U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX1166330: GSM1862952: PCF RiboProf replicate_3 reanalysis; Trypanosoma brucei; RNA-Seq
1 ILLUMINA (Illumina Genome Analyzer II) run: 64.6M spots, 2.3G bases, 1.3Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Advancing Trypanosoma brucei genome annotation through ribosome profiling and spliced leader mapping
show Abstracthide Abstract
Since the initial publication of the trypanosomatid genomes, curation has been ongoing. Here we apply the technique of ribosome profiling to Trypanosoma brucei, identifying 223 new coding regions by virtue of ribosome occupancy in the corresponding transcripts. A small number of these putative genes correspond to extra copies of previously annotated genes but 85% are novel. The median size of these novels CDSs is small (74 aa) indicating that past annotation work has excelled at detecting large CDSs. Of the unique CDSs discovered here, over half have candidate orthologues in other trypanosomatid genomes, most of which were not yet annotated as genes. Still, approximately one-third of the new CDSs were found only in T. brucei subspecies. When combined with RNA-seq and spliced leader mapping, we were able to definitively revise the start sites for 430 CDSs as compared to the current gene models. Such data also allowed us to use a structured approach to eliminate 701 putative genes as protein-coding. Finally, the data pointed to several regions of the genome that had sequence errors that altered coding region boundaries. Overall design: Ribosome profiling and mRNA libraries were constructed in triplicate from in vitro PCF and in vivo BF lifestages of theT. brucei Treu927 and in vitro T. brucei Lister427, to evaluate role of translational gene regulation
Sample: PCF RiboProf replicate_3 reanalysis
SAMN04014719 • SRS1046665 • All experiments • All runs
Library:
Instrument: Illumina Genome Analyzer II
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: For in vivo blood form parasites, the blood from 2-3 infects rats was pooled and centrifuged and the buffy coat extracted and placed into 20 ml HMI-9 without serum pre-warmed to 37°C. To arrest translation, cycloheximide was added to 100 μg/ml and incubated for 2 minutes at 37°. To rapidly chill the cells, 300 ml of ice-cold phosphate buffered saline with glucose (PSG) was added and the cells were pelleted at 4°. Only parasite populations with greater than 99% slender cells were used. In vitro grown parasites were pelleted at 5000g and resuspended in 50 mls of media lacking serum. Cycloheximide was added to 100 mg/ml at the cell incubated for 2min at room temperature (procyclic cells) or 37° (bloodform cells). Following cycloheximide treatment the cells were rapidly chilled with PSG and pelleted at 5000g. Lysates from both type of parasite pellets were then prepared as following. Cell pellets were resuspended in Buffer A (10 mM Tris pH 7.4, 300 mM KCl, 10 mM MgCl2 plus protease inhibitors to approximately 1.3x109/ml. Approximately one-third of the sample was placed into TRIzol (Life Technologies) for RNA extraction following manufacturer’s suggested protocol. To the remainder, one-sixth volume of buffer A containing 0.2M sucrose and 1.2% Triton N-101 was added and the samples were dounced (30 strokes in a chilled homogenizer). After transfer to a prechilled microfuge tube, the samples were clarified by centrifugation in a microfuge at 15000 rpm for one minute. The supernatant was withdrawn, pooled if needed, and then aliquots flash frozen in liquid nitrogen for storage at -70°C. After thawing on ice, RNase I (Ambion) was added at 30 units/OD260 of lysate. Samples were then incubated for 1 hour at room temperature. RNase digestion was stopped by adding 400 units RNasin (Promega). Samples were them layered over a 1 ml 1M sucrose cushion prepared in buffer A and ribosomes were pelleted by centrifuging for 4 hours at 70,000g in an SW55 rotor. After removing the supernatant, the ribosomal pellet was resuspended in 500 μl buffer A with the MgCl2 replaced with 10 mM EDTA to dissociate the ribosomes and deplete larger rRNA fragments. The protected fragments were then separated from contaminating ribosomal RNA by passage through an Amicon Ultra-4 or YM-100 column with 100,000 MW cutoff. After more than 400 μl had flowed through the membrane the RNA in the flow-through was extracted with phenol:CHCl3:iAA and the RNA precipitated. Poly(A)+ RNA was isolated using Dynabeads mRNA Direct (Life Technologies). RNA was fragmented as described Ingolia et all 2011. Ribosomal protected fragments between 28 and 31 nucleotides and fragmented Poly(A)+ RNA between 30 and 70 nucleotides was isolated from 15% accrylimide gels and libraries prepared for sequencing. For detailed protocol on generating sequencing libraries for both the ribosome protected and fragmented mRNA library see Ingolia et a 2011. Briefly, following dephosphorylation the adapter Linker-1 (IDT) was ligated to the 3’ end of the fragment and the ligated product gel purified. The adapter was used for priming reverse. Following gel purification the cDNA was circularized with Circ Ligase (Epicenter Biotechnologies). Circles containing ribosomal RNA were subtracted using biotinylated primers . The final library was generated by PCR..To map the 5’ end of the transcripts, libraries enriched for the 5’ ends of mRNAs were constructed from three biological samples of strain 927 (2 PCF and 1 slBF selected from the biological samples above). SL libraries were constructed as described Mittra B et al 2013. In brief, RNA was prepared and cDNA synthesized using primer ending in a random 6 bases. Second strand synthesis was primed using a primer that matches the T. brucei SL sequence. The sequencing library was generated by PCR. Duplexed libraries were sequenced using Illumina GA II machines at the High Throughput Genomics Unit at the University of Washington to generate ~36 nt reads. RNAseq, Ribosome Profiling Seq, Splice Leader RNAseq
Experiment attributes:
GEO Accession: GSM1862952
Links:
Runs: 1 run, 64.6M spots, 2.3G bases, 1.3Gb
Run# of Spots# of BasesSizePublished
SRR218808864,636,1892.3G1.3Gb2015-12-22

ID:
1697033

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...