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Basic Study
Copyright: ©Author(s) 2026.
World J Diabetes. Apr 15, 2026; 17(4): 115842
Published online Apr 15, 2026. doi: 10.4239/wjd.v17.i4.115842
Figure 1
Figure 1 Molecular and genetic features of one Chinese pedigree with type 2 diabetes. A: One family with maternally transmitted diabetes, arrow indicates the proband; B: Sequence analysis of the m.C15954T mutation. WT: Wild type; MT: Mutant.
Figure 2
Figure 2 Secondary structures of mitochondrial-tRNAThr and mitochondrial-tRNAPro genes, arrow indicates the position of 15954. Processing sites in mitochondrial (mt)-tRNAThr and mt-tRNAPro precursors were determined for tRNase Z.
Figure 3
Figure 3 Mitochondrial-transfer RNAs analyses. A: Analysis of the steady-state levels of mitochondrial (mt)-tRNAThr and mt-tRNAPro in control and mutant cell lines by Northern blot; B: Qualifications of mt-transfer RNA levels, the average relative transfer RNAs content were normalized to the average content per cell of 5S rRNA. tRNA: Transfer RNA.
Figure 4
Figure 4 Analysis of mitochondrial-RNA transcription in control and mutant cell lines.
Figure 5
Figure 5 Analysis of mitochondrial DNA copy number, adenosine triphosphate, mitochondrial membrane potential and reactive oxygen species levels in 15954C and 15954T cybrids. A: Mitochondrial DNA copy number; B: Adenosine triphosphate; C: Mitochondrial membrane potential; D: Reactive oxygen species. mtDNA: Mitochondrial DNA; ATP: Adenosine triphosphate; MMP: Mitochondrial membrane potential; ROS: Reactive oxygen species.
Figure 6
Figure 6 Analysis of oxidative phosphorylation enzymatic activities in 15954C and 15954T cybrids. CI-CIV: Complex I-IV; C: Control; M: Mutant.