MTOR regulates DNA damage response through NF-κB-mediated FANCD2 pathway in hematopoietic cells

F. Guo, J. Li, W. Du, S. Zhang, M. O'Connor, G. Thomas, S. Kozma, B. Zingarelli, Q. Pang, Y. Zheng

Research output: Contribution to journalArticlepeer-review

63 Scopus citations


Hematopoietic stem/progenitor cells (HSPCs) function to give rise to mature blood cells. Effective DNA damage response (DDR) and maintenance of genomic stability are crucial for normal functioning of HSPCs. Mammalian target of rapamycin (mTOR) integrates signals from nutrients and growth factors to control protein synthesis, cell growth, survival and metabolism, and has been shown to regulate DDR in yeast and human cancer cells through the p53/p21 signaling cascade. Here, we show that gene targeting of mTOR in HSPCs causes a defective DDR due to a variety of DNA damage agents, mimicking that caused by deficient FANCD2, a key component of the Fanconi anemia (FA) DDR machinery. Mechanistically, mTOR -/- HSPCs express drastically reduced FANCD2. Consistent with these genetic findings, inactivation of mTOR in human lymphoblast cells by pp242 or Torin 1, mTOR kinase inhibitors, suppresses FANCD2 expression and causes a defective DDR that can be rescued by reconstitution of exogenous FANCD2. Further mechanistic studies show that mTOR deficiency or inactivation increases phosphorylation and nuclear translocation of nuclear factor (NF)-κB, which results in an enhanced NF-κB binding to FANCD2 promoter to suppress FANCD2 expression. Thus, mTOR regulates DDR and genomic stability in hematopoietic cells through a noncanonical pathway involving NF-κB-mediated FANCD2 expression.

Original languageEnglish (US)
Pages (from-to)2040-2046
Number of pages7
Issue number10
StatePublished - Oct 2013

Bibliographical note

Funding Information:
We thank Dr Markus Grompe (Oregon Health & Sciences University) for FANCD2+/− mice, Dr Alan D’Andrea (Harvard Medical School) for the pMMP-Puro and pMMP-FANCD2 retroviral vectors. This work was supported by NIH grants R01 HL076712 and T32 HL091805.


  • DNA damage response
  • FANCD2
  • NF-kB
  • hematopoietic cells
  • mTOR


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