Identification of Atg5-dependent transcriptional changes and increases in mitochondrial mass in Atg5-deficient T lymphocytes

Identification of Atg5-dependent transcriptional changes and increases in mitochondrial mass in Atg5-deficient T lymphocytes

2009; 5(5) | Linda M. Stephenson, Brian C. Miller, Aylwin Ng, Jason Eisenberg, Zijiang Zhao, Ken Cadwell, Daniel B. Graham, Noboru N. Mizushima, Ramnik Xavier, Herbert W. Virgin, Wojciech Swat
The supplemental material provides additional data and analysis supporting the main findings of the study. Figure S1 shows that Atg5-deficient chimeras have significantly reduced survival compared to Atg5野生型 chimeras, with a p-value indicating statistical significance. Figure S2 demonstrates the recombination of the Atg5flx allele in Atg5F/F Cre+ thymocytes through PCR analysis. Supplemental Figure 3 includes two heatmaps: (A) mitochondrial functions and (B) general cellular processes or specific T-lineage immune functions, generated from literature co-citation analysis of differentially expressed genes. The intensity of red in the heatmaps indicates the extent to which each gene is co-cited with specific terms in the PubMed database.The supplemental material provides additional data and analysis supporting the main findings of the study. Figure S1 shows that Atg5-deficient chimeras have significantly reduced survival compared to Atg5野生型 chimeras, with a p-value indicating statistical significance. Figure S2 demonstrates the recombination of the Atg5flx allele in Atg5F/F Cre+ thymocytes through PCR analysis. Supplemental Figure 3 includes two heatmaps: (A) mitochondrial functions and (B) general cellular processes or specific T-lineage immune functions, generated from literature co-citation analysis of differentially expressed genes. The intensity of red in the heatmaps indicates the extent to which each gene is co-cited with specific terms in the PubMed database.
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