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The transcription factor CBFB suppresses breast cancer through orchestrating translation and transcription.

Navdeep MalikHualong YanNellie MoshkovichMurali PalangatHoward YangVanesa SanchezZhuo CaiTyler J PeatShunlin JiangChengyu LiuMaxwell LeeBeverly A MockStuart H YuspaDaniel R LarsonLalage M WakefieldJing Huang
Published in: Nature communications (2019)
Translation and transcription are frequently dysregulated in cancer. These two processes are generally regulated by distinct sets of factors. The CBFB gene, which encodes a transcription factor, has recently emerged as a highly mutated driver in a variety of human cancers including breast cancer. Here we report a noncanonical role of CBFB in translation regulation. RNA immunoprecipitation followed by deep sequencing (RIP-seq) reveals that cytoplasmic CBFB binds to hundreds of transcripts and regulates their translation. CBFB binds to mRNAs via hnRNPK and enhances translation through eIF4B, a general translation initiation factor. Interestingly, the RUNX1 mRNA, which encodes the transcriptional partner of CBFB, is bound and translationally regulated by CBFB. Furthermore, nuclear CBFB/RUNX1 complex transcriptionally represses the oncogenic NOTCH signaling pathway in breast cancer. Thus, our data reveal an unexpected function of CBFB in translation regulation and propose that breast cancer cells evade translation and transcription surveillance simultaneously through downregulating CBFB.
Keyphrases
  • transcription factor
  • signaling pathway
  • dna binding
  • single cell
  • endothelial cells
  • cell proliferation
  • gene expression
  • copy number
  • dna methylation
  • oxidative stress
  • hiv infected
  • lymph node metastasis