Talaromyces marneffei suppresses macrophage inflammation by regulating host alternative splicing
© 2023. Springer Nature Limited..
Talaromyces marneffei (T. marneffei) immune escape is essential in the pathogenesis of talaromycosis. It is currently known that T. marneffei achieves immune escape through various strategies. However, the role of cellular alternative splicing (AS) in immune escape remains unclear. Here, we depict the AS landscape in macrophages upon T. marneffei infection via high-throughput RNA sequencing and detect a truncated protein of NCOR2 / SMRT, named NCOR2-013, which is significantly upregulated after T. marneffei infection. Mechanistic analysis indicates that NCOR2-013 forms a co-repression complex with TBL1XR1 / TBLR1 and HDAC3, thereby inhibiting JunB-mediated transcriptional activation of pro-inflammatory cytokines via the inhibition of histone acetylation. Furthermore, we identify TUT1 as the AS regulator that regulates NCOR2-013 production and promotes T. marneffei immune evasion. Collectively, these findings indicate that T. marneffei escapes macrophage killing through TUT1-mediated alternative splicing of NCOR2 / SMRT, providing insight into the molecular mechanisms of T. marneffei immune evasion and potential targets for talaromycosis therapy.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:6 |
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| Enthalten in: |
Communications biology - 6(2023), 1 vom: 16. Okt., Seite 1046 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Wei, Wudi [VerfasserIn] |
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| Anmerkungen: |
Date Completed 23.10.2023 Date Revised 19.11.2023 published: Electronic Citation Status MEDLINE |
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| doi: |
10.1038/s42003-023-05409-6 |
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| PPN (Katalog-ID): |
NLM363381414 |
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| 520 | |a © 2023. Springer Nature Limited. | ||
| 520 | |a Talaromyces marneffei (T. marneffei) immune escape is essential in the pathogenesis of talaromycosis. It is currently known that T. marneffei achieves immune escape through various strategies. However, the role of cellular alternative splicing (AS) in immune escape remains unclear. Here, we depict the AS landscape in macrophages upon T. marneffei infection via high-throughput RNA sequencing and detect a truncated protein of NCOR2 / SMRT, named NCOR2-013, which is significantly upregulated after T. marneffei infection. Mechanistic analysis indicates that NCOR2-013 forms a co-repression complex with TBL1XR1 / TBLR1 and HDAC3, thereby inhibiting JunB-mediated transcriptional activation of pro-inflammatory cytokines via the inhibition of histone acetylation. Furthermore, we identify TUT1 as the AS regulator that regulates NCOR2-013 production and promotes T. marneffei immune evasion. Collectively, these findings indicate that T. marneffei escapes macrophage killing through TUT1-mediated alternative splicing of NCOR2 / SMRT, providing insight into the molecular mechanisms of T. marneffei immune evasion and potential targets for talaromycosis therapy | ||
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| 700 | 1 | |a Wang, Gang |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Hong |e verfasserin |4 aut | |
| 700 | 1 | |a Bao, Xiuli |e verfasserin |4 aut | |
| 700 | 1 | |a An, Sanqi |e verfasserin |4 aut | |
| 700 | 1 | |a Luo, Qiang |e verfasserin |4 aut | |
| 700 | 1 | |a He, Jinhao |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Lixiang |e verfasserin |4 aut | |
| 700 | 1 | |a Ning, Chuanyi |e verfasserin |4 aut | |
| 700 | 1 | |a Lai, Jingzhen |e verfasserin |4 aut | |
| 700 | 1 | |a Yuan, Zongxiang |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Rongfeng |e verfasserin |4 aut | |
| 700 | 1 | |a Jiang, Junjun |e verfasserin |4 aut | |
| 700 | 1 | |a Ye, Li |e verfasserin |4 aut | |
| 700 | 1 | |a Liang, Hao |e verfasserin |4 aut | |
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