28S-rsRNA facilitates PASMC proliferation through PKM2 β-hydroxybutyrylation

Liu, A.; Wang, Y.; Pan, Y.; Zhang, J.; Liu, C.; Liao, X.; Bai, J.; Sun, H.; Zhao, X.; Bao, Z.; Zhu, H.; Ji, Y.; Xu, Y.; Xing, Y.; Tang, H.; Zhu, D.; Yu, H.

doi:10.64898/2026.11.09.765510

bioRxiv · 10.64898/2026.11.09.765510

28S-rsRNA facilitates PASMC proliferation through PKM2 β-hydroxybutyrylation

Liu, A.·Wang, Y.·Pan, Y.·Zhang, J.·Liu, C.·Liao, X.·Bai, J.·Sun, H.·Zhao, X.·Bao, Z.·Zhu, H.·Ji, Y.·Xu, Y.·Xing, Y.·Tang, H.·Zhu, D.·Yu, H.

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Abstract

Ribosomal RNA-derived small RNAs (rsRNAs) are nucleic acid fragments originating from rRNA, the functions and roles of which in diseases remain incompletely understood. We identified 28S rsRNA-CTC_L20, an rsRNA whose expression is upregulated in hypoxic pulmonary artery smooth muscle cells (PASMCs) and in lung tissues of pulmonary hypertension (PH) models. In hypoxic cells, 28S rsRNA-CTC_L20 promotes PASMC proliferation, and its knockdown mitigates SuHx-induced pulmonary hypertension and vascular remodeling. Mechanistically, 28S rsRNA-CTC_L20 modulates {beta}-hydroxybutyrate (BHB) production by maintaining the stability of ketogenic enzyme mRNAs through its "CTGNNGG" motif. Elevated levels of BHB enhance the {beta}-hydroxybutyrylation modification at K166 of pyruvate kinase M2 (PKM2), increasing its activity and driving glycolysis to sustain proliferation. These results link ketone body metabolism to glycolysis in hypoxic cells and define an rsRNA-BHB-PKM2 {beta}-hydroxybutyrylation axis in PH. They also point to 28S rsRNA-CTC_L20 as a potential target for treating vascular remodeling.

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Liu, A., Wang, Y., Pan, Y., Zhang, J., Liu, C., Liao, X., Bai, J., Sun, H., Zhao, X., Bao, Z., Zhu, H., Ji, Y., Xu, Y., Xing, Y., Tang, H., Zhu, D., Yu, H.. 2026-11-11. 28S-rsRNA facilitates PASMC proliferation through PKM2 β-hydroxybutyrylation. https://doi.org/10.64898/2026.11.09.765510

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