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TANGO6 regulates cell proliferation via COPI vesicle-mediated RPB2 nuclear entry.

Zhi FengShengnan LiuMing SuChunyu SongChenyu LinFangying ZhaoYang LiXianyan ZengYong ZhuYu HouChunguang RenHuan ZhangPing YiYong JiChao WangHongtao LiMing MaLingfei LuoLi Li
Published in: Nature communications (2024)
Coat protein complex I (COPI) vesicles mediate the retrograde transfer of cargo between Golgi cisternae and from the Golgi to the endoplasmic reticulum (ER). However, their roles in the cell cycle and proliferation are unclear. This study shows that TANGO6 associates with COPI vesicles via two transmembrane domains. The TANGO6 N- and C-terminal cytoplasmic fragments capture RNA polymerase II subunit B (RPB) 2 in the cis-Golgi during the G1 phase. COPI-docked TANGO6 carries RPB2 to the ER and then to the nucleus. Functional disruption of TANGO6 hinders the nuclear entry of RPB2, which accumulates in the cytoplasm, causing cell cycle arrest in the G1 phase. The conditional depletion or overexpression of TANGO6 in mouse hematopoietic stem cells results in compromised or expanded hematopoiesis. Our study results demonstrate that COPI vesicle-associated TANGO6 plays a role in the regulation of cell cycle progression by directing the nuclear transfer of RPB2, making it a potential target for promoting or arresting cell expansion.
Keyphrases
  • cell cycle
  • endoplasmic reticulum
  • cell proliferation
  • stem cells
  • pi k akt
  • cell cycle arrest
  • cell therapy
  • signaling pathway
  • estrogen receptor
  • breast cancer cells
  • transcription factor
  • small molecule