|
Status |
Public on Jun 25, 2020 |
Title |
yeast unselected 80S 1-2 |
Sample type |
SRA |
|
|
Source name |
cell culture
|
Organism |
Saccharomyces cerevisiae |
Characteristics |
strain: H25 (eIF3c/NIP1-FLAG) rna fragment size selection: approximately 18 to 85 co-ip: no protocol: RNA 80S footprint
|
Treatment protocol |
incubation of the cell culture with 0.8 % w/v formaldehyde on ice for 1 h
|
Growth protocol |
in 1 litre YPD at 30ºC up to OD600 of ~0.7-0.8
|
Extracted molecule |
total RNA |
Extraction protocol |
cell lysis with bead beater, RNase I digestion to generate ribosomal footprints, 40S/80S separation (followed by Co-IP if indicated), hot acid phenol RNA extraction library construction according to Ingolia et al., 2010, Methods Enzymol (different RNA fragment size selection, different set of rRNA depletion oligos)
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|
|
Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
Library strategy: TCP-seq Illumina CASAVA 1.8 for base calling adapter trimming (fastx_clipper of FASTX Toolkit 0.0.13), filtering by alignment to rRNA (bowtie 1.2.2) and ncRNA, tRNA (bowtie2 2.2.6) alignment to transcriptome Ensembl R64-1-1.80 (with 3’ UTR, 5’ UTR, and 5’ UTR intron annotation from SGD) and genome R64-1-1 with TopHat 2.1.0 Genome_build: R64-1-1 Supplementary_files_format_and_content: metagene_FP5end_AUG_-80+30_FPlength.tbl; counts of footprint 5’ ends positioned from -80 nt to +30 nt relative to the AUG start codon (over rows) respecting the footprint length (18 – 98 nt over columns) Supplementary_files_format_and_content: metagene_FP5end_STOP_-80+30_FPlength.tbl; counts of footprint 5’ ends positioned from -80 nt to +30 nt relative to the STOP codon (over rows) respecting the footprint length (18 – 98 nt over columns) Supplementary_files_format_and_content: metagene_coverage_CAP_-40+40.csv; footprint coverage from -40 nt to +40 nt relative to the transcript start Supplementary_files_format_and_content: genewise_FPcount_transcript_area.csv; footprint count per transcript area Supplementary_files_format_and_content: genewise_mean_CI_FP5end_FP3end_AUG_-50+50.ods; distribution (mean and 95 percentiles) of footprint 5’end and 3’end positions relative to the AUG start codon of start codon associated footprints without 5’extension (footprint 5’end from -12 to -14 nt) Supplementary_files_format_and_content: genewise_mean_CI_FP5end_FP3end_AUG_-50+50_all_AUG_associated_FPs.ods; distribution (mean and 95 percentiles) of footprint 5’end and 3’end positions relative to the AUG start codon of start codon associated footprints Supplementary_files_format_and_content: coverage_GCN4_YEL009C_-50.csv; coverage for the 5’UTR and the beginning of the CDS for GCN4 (starting at -50 nt from the transcript start) Supplementary_files_format_and_content: coverage_for_co-translational_assembly.ods; coverage for eIF3a, eIF3b, eIF3g and eIF2beta of 80S footprints and eIF3a/c bound 80S footprints (starting at -50 nt from transcript start)
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|
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Submission date |
Oct 20, 2019 |
Last update date |
Jun 25, 2020 |
Contact name |
Susan Wagner |
E-mail(s) |
[email protected]
|
Organization name |
Australian National University
|
Department |
The John Curtin School of Medical Research
|
Lab |
RNA Biology - Preiss Group
|
Street address |
131 Garran Road
|
City |
Canberra |
State/province |
ACT |
ZIP/Postal code |
2601 |
Country |
Australia |
|
|
Platform ID |
GPL17342 |
Series (2) |
GSE139130 |
Selective Translation Complex Profiling in yeast and human Reveals Staged Initiation and Co-translational Assembly of Initiation Factor Complexes [Yeast] |
GSE139132 |
Selective Translation Complex Profiling in yeast and human Reveals Staged Initiation and Co-translational Assembly of Initiation Factor Complexes |
|
Relations |
BioSample |
SAMN13065535 |
SRA |
SRX7026369 |