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Figure 1

From: Enhanced skeletal muscle ribosome biogenesis, yet attenuated mTORC1 and ribosome biogenesis-related signalling, following short-term concurrent versus single-mode resistance training

Figure 1

Overview of the role of mTORC1 signalling in promoting ribosome biogenesis following a single session of resistance exercise, and the potential effect of incorporating endurance training (i.e., performing concurrent training). Adapted with permission from24. Ribosome biogenesis involves transcription of the 45S rRNA (ribosomal RNA) precursor (45S pre-rRNA) (A) mediated by RNA Polymerase I (Pol-I), processing of the 45S pre-rRNA into several smaller rRNAs (18S, 5.8S and 28S rRNAs) (B), assembly of these rRNAs and other ribosomal proteins into ribosomal subunits (40S and 60S) (C), and nuclear export of these ribosomal subunits into the cytoplasm24,26 (D). As well as regulating translational efficiency via downstream control of p70S6K (p70 kDa ribosomal protein subunit kinase 1) and 4E-BP1 (eukaryotic initiation factor 4E binding protein 1) (E), mTORC1 is a key mediator of ribosome biogenesis by regulating transcription factors for genes encoding RNA Pol-I (and also RNA Pol-II and –III, which are not shown in figure)25. Transcription of the 45S pre-rRNA by RNA Pol-I requires a transcriptional complex including TIF-1A (transcription initiation factor 1A; also known as RRN5) and UBF (upstream binding factor), both of which are regulated by the mTORC1 pathway28,29 (F). Activation of AMPK is known to inhibit mTORC1 signalling in rodent skeletal muscle64, and AMPK activation in skeletal muscle is traditionally associated with endurance-type exercise. However, whether signalling events initiated by endurance training, when performed concurrently with resistance training, have the potential to interfere with mTORC1-mediated regulation of ribosome biogenesis is currently unclear (G).

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