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Series GSE84913 Query DataSets for GSE84913
Status Public on Sep 08, 2016
Title Accessory subunits are integral for assembly and function of human mitochondrial complex I
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary For analysis of mRNA expression levels, total RNA was harvested from each cell-line in replicate with Trizol™ (Thermo scientific). Total RNA was purified using Direct-zol™ columns according to the manufacturers specifications (Zymo Research). For cDNA synthesis 1 μg of total RNA was process as the T12VN-PAT assay (Jänicke et al., RNA 2012), except that this was adapted for multiplexing on the Illumina MiSeq instrument. We refer to this assay as mPAT for multiplexed PAT. The approach is based on a nested-PCR that sequentially incorporates the Illumina platform’s flow-cell specific terminal extensions onto 3’ RACE PCR amplicons. First, cDNA was generated using the anchor primer mPAT Reverse, next this primer and a pool of 50 gene-specific primers were used in 5 cycles of amplification. Each gene-specific primer had a universal 5’ extension (see supplementary file primers) for sequential addition of the 5’ (P5) Illumina elements. These amplicons were then purified using NucleoSpin columns (Macherey-Nagel), and entered into second round amplification using the universal Illumina Rd1 sequencing Primer and TruSeq indexed reverse primers from Illumina. Second round amplification was for 14 cycles. Note, that each experimental condition was amplified separately in the first round with identical primers. In the second round, a different indexing primer was used for each experimental condition. All PCR reactions were pooled and run using the MiSeq Reagent Kit v2 with 300 cycles (i.e. 300 bases of sequencing) according to the manufacturers specifications. Data were analysed using established bioinformatics pipelines (Harrison et al., RNA 2015)
 
Overall design Quantitation of a custom set of amplicons for the Accessory subunits of human mitochondrial complex I.
 
Contributor(s) Ryan M, Harrrison PF, Beilharz TH
Citation(s) 27626371
Submission date Jul 27, 2016
Last update date May 15, 2019
Contact name Traude Beilharz
E-mail(s) traude.beilharz@monash.edu
Organization name Monash University
Department Biomedicine Discovery Institute
Lab RNA Systems Biology Laboratory
Street address Wellington Rd
City Clayton
State/province VIC
ZIP/Postal code 3800
Country Australia
 
Platforms (1)
GPL15520 Illumina MiSeq (Homo sapiens)
Samples (24)
GSM2253955 HEK293T-R1
GSM2253956 HEK293T-R2
GSM2253957 FV3-R1
Relations
BioProject PRJNA335626
SRA SRP079980

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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE84913_counts.csv.gz 3.4 Kb (ftp)(http) CSV
GSE84913_regions.gff.gz 1.4 Kb (ftp)(http) GFF
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Raw data are available in SRA
Processed data are available on Series record

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