Data highlighting miR-155 and GAPDH correlation

This data represents the effect of miR-155 on the expression of commonly used housekeeping genes, GAPDH, Beta Actin, RPL13A, and U6. The human miR-155 and control RNA were transfected to A549 cells by electroporation. Expression of these genes was compared in both groups by real-time PCR. The significant up-regulation in the expression of GAPDH was observed in the miR-155 transfected samples as compared to control while no major change was observed in the expression of the other three genes.

Chain Reaction (qPCR) method. The qPCR efficiency, represented in Table 1, of each primer, was assessed by making the standard curve. The expression profiling of all four genes in control and miR-155 transfected samples shows a significant (p < 0.001) difference in the expression of gene GAPDH as compared to other test genes ( Table 2). The data presented in Table 2 is Ct value data of qPCR performed on the cDNA sample obtained from A549 cells transfected with miR-155 and the cell transfected with negative control RNA. The Ct value representing in Table 2 is the average of technical replicates for each sample. Fig. 1 shows the upregulation in the expression of gene GAPDH in the miR-155 transfected group as compared to the control group while no critical change observed in the expression of other genes. The experiment performed on three biological and three technical replicates of each sample using primers in Table 3.

Culture of human alveolar epithelial cell lineA549
Human alveolar epithelial cell line (A549) was maintained in Dulbecco's Modified Eagle Medium (DMEM) containing 10% fetal bovine serum (FBS), 100 units/ml penicillin, and 100 units/ml streptomycin in tissue culture flasks at 37 C with 5% CO 2.  Value of the data The data represents a correlation between miR-155 and GAPDH expression. Since the GAPDH is an essential enzyme of the glycolysis pathway, therefore the association of miR-155 with glycolytic pathways may be explored. The data will help in choosing better housekeeping genes for miR-155 transfection experiments. The data is valuable for those working on microRNA electroporation.    (hsa-miR-155e5p mimic (Catalog # 4464066, Assay ID MC12601, Thermo scientific), Negative control microRNA (Catalog# 4464077, Thermo Scientific)) in electroporation buffer was 30nM. Electroporation was performed in 0.2ml Cuvette at 150V for 10 ms in a single pulse. Cells were seeded in six well plate after electroporation.

RNA isolation, cDNA preparation and real-time PCR
Total RNA was isolated using miRVANA RNA isolation kit (Catalog# AM1560, Thermo scientific) as per manufacturer's instructions. RNA quantification was done by qubit 3.0 fluorometer (Catalog #Q33216, life technologies). Total RNA (1mg) was reverse transcribed using high capacity reverse transcription kit (Catalog# 4368814, Thermo scientific) with oligo dT primer. PCR reaction (20ml) for the genes GAPDH, Beta Actin and RPL13A was performed using 2 ml of cDNA, 10 mlSSo Fast Eva green (Catalog# 1725203, Bio-Rad) and 0.25pmol primer mix (forward and reverse) on CFX96 Touch realtime PCR system (Catalog# 1855195, Bio-Rad) with temperature conditions as follow: Initial denaturation at 98 C for 2min followed by 30 cycles of 98 C for 5 sec and 60 C for 5 sec.
The reverse transcription and PCR reaction of U6 was performed using predesigned assay (assay ID 001973, Thermo Scientific) as per the manufacturer instruction. Briefly, 10ng total RNA was reverse transcribed using RT primer with TaqMan reverse transcription kit (Catalog# 4366596, Applied Biosystems). PCR reaction was performed using a specific Taq Man primer-probe set by PCR master mix (Catalog# 4324018, Applied Biosystems).
The Ct value data was collected by CFX manager software (Bio-rad).

Primer efficiency calculation
PCR reaction was performed for each gene of Table 1, using 2 ml cDNA. The PCR product of each gene was run on the agarose gel, DNA band was excised from the agarose gel and purified using gel extraction kit (Catalog# 28115, Qiagen) as per the manufacturer's instructions. The 10-fold serial dilution of all purified DNA samples was prepared and amplified by real-time PCR using the specific primer to generate a standard curve. Primer efficiency was calculated from the slop using formula. E ¼ 10 Àð1=slopeÞ À 1

Statistical analysis
Unpaired T-test was applied on the 2 ÀDCt value of the data obtained from the samples transfected with negative control and miR-155.