Splicing factor proline- and glutamine-rich (SFPQ) protein causes transcriptional repression of SNAIL to counteract

Niyati Pandya Thakkar1, Hariharan Jayakumar1, S Ramakrishnan1

  • 1Department of Biological Sciences, Birla Institute of Technology and Science (BITS) Pilani, Pilani Campus, Rajasthan, India.

Insights

Splicing factor proline- and glutamine-rich (SFPQ) acts as a novel repressor of Snail, a key gene in TGF-β signaling. This study reveals SFPQ

Area of Science:

  • Cellular Biology
  • Molecular Biology
  • Signaling Pathways

Background:

  • Transforming growth factor-beta (TGF-β) signaling is crucial for cellular functions but its uncontrolled activation contributes to human diseases.
  • Maintaining cellular homeostasis requires counter-regulatory mechanisms to balance TGF-β downstream signaling.
  • Snail is an immediate-early response gene transcriptionally regulated by TGF-β signaling via Smad complexes.

Purpose of the Study:

  • To identify novel regulators of TGF-β-induced Snail expression.
  • To investigate the role of Splicing factor proline- and glutamine-rich (SFPQ) in TGF-β signaling and Snail regulation.

Main Methods:

  • Assessed SFPQ expression in a pro-fibrotic rat model and in endothelial cells (ECs) treated with TGF-β.
  • Investigated SFPQ regulation via ubiquitination, proteasomal degradation, and subcellular localization.
  • Utilized SFPQ knockdown and overexpression studies, co-immunoprecipitation, and Chromatin Immunoprecipitation quantitative PCR (ChIP-qPCR).

Main Results:

  • TGF-β stimulation decreased SFPQ protein levels in ECs through ubiquitination-dependent proteasomal degradation and cytosolic translocation.
  • SFPQ functions as a transcriptional repressor of Snail, with SFPQ knockdown enhancing and overexpression suppressing TGF-β-induced Snail expression.
  • SFPQ binds to the Snail promoter region, independent of Smad or N1-ICD interactions.

Conclusions:

  • SFPQ acts as a novel transcriptional repressor of Snail, modulating TGF-β-induced responses.
  • SFPQ degradation and cytosolic translocation are key post-translational mechanisms regulating its function in TGF-β signaling.
  • SFPQ represents a potential therapeutic target for diseases associated with dysregulated TGF-β signaling.

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