AI Article Synopsis

  • The FUBP1 protein, known for binding single-stranded DNA, has a role in activating MYC transcription, while its counterpart Psi in Drosophila binds RNA to regulate splicing and promote growth.
  • Psi not only activates MYC for cell growth but also directly binds stg to synchronize growth with cell division, with its knockdown leading to reduced division in wing imaginal discs.
  • Psi also represses the growth inhibitor gene tolkin, and manipulation of tok levels affects cell proliferation, demonstrating that Psi manages growth by activating pro-proliferative genes and repressing inhibitors.

Article Abstract

The first characterised FUSE Binding Protein family member, FUBP1, binds single-stranded DNA to activate MYC transcription. Psi, the sole FUBP protein in Drosophila, binds RNA to regulate P-element and mRNA splicing. Our previous work revealed pro-growth functions for Psi, which depend, in part, on transcriptional activation of Myc. Genome-wide functions for FUBP family proteins in transcriptional control remain obscure. Here, through the first genome-wide binding and expression profiles obtained for a FUBP family protein, we demonstrate that, in addition to being required to activate Myc to promote cell growth, Psi also directly binds and activates stg to couple growth and cell division. Thus, Psi knockdown results in reduced cell division in the wing imaginal disc. In addition to activating these pro-proliferative targets, Psi directly represses transcription of the growth inhibitor tolkin (tok, a metallopeptidase implicated in TGFβ signalling). We further demonstrate tok overexpression inhibits proliferation, while tok loss of function increases mitosis alone and suppresses impaired cell division caused by Psi knockdown. Thus, Psi orchestrates growth through concurrent transcriptional activation of the pro-proliferative genes Myc and stg, in combination with repression of the growth inhibitor tok.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110491PMC
http://dx.doi.org/10.1242/dev.201563DOI Listing

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