Skip to content
DraconiticResearch
Search Sources API
194,161 studies31 sourcesUpdated 17 min ago
PreprintCC BY-NC-ND 4.0HAL

Lineage-specific regulation and RNA-associated functions of SATB1 in mature B-cells

Abstract

Special AT-rich binding protein 1 (SATB1) is a nuclear matrix-associated transcription factor that orchestrates higher-order chromatin architecture and gene expression in T and B lymphocytes. While SATB1’s role in T cells is well-established, its regulation and function in B cells remain underexplored. Here, we showed that Satb1 expression in mature B cells is controlled by alternative promoter usage and splicing, with promoters P1 and P3 dynamically switching upon LPS-induced activation, while P2 remains transcriptionally silent. We identified four Satb1 mRNA isoforms, including two novel transcripts ( Δ9 and Δ9Δ11 ), all of which maintain open reading frames. Satb1 transcription decreases upon activation while SATB1 protein content evolves differently, suggesting post-transcriptional regulation. SATB1 forms a high-molecular-weight complex in B cells, and co-immunoprecipitation mass spectrometry reveals RNA-binding proteins as its predominant interactors. These findings specify SATB1 expression kinetics during B-cell activation and reveal its role as a regulator of RNA splicing in B cells.

Related

  1. CREST functions as a molecular bridge between neuron-specific enhancers and epigenetic regulators in mature motor neurons
    Kaitlin N. Montanera, Andrew J. Lee, Woobin Yun +4
    Nature CommunicationsPeer-reviewedCC BY 4.0Full textMolecular biology & gene regulationCrossref
  2. Histone Acetylation in Bone Remodeling: Metabolic Regulation, Lineage-Specific Chromatin Programs, and Therapeutic Implications
    Jianhong Dong, Xianji Wei, Yifan Qian +2
    CellsPeer-reviewedCC BY 4.0Molecular biology & gene regulationCrossref
  3. miRNA-mediated regulation of lineage plasticity in YY1 knockout pro-B cells
    N. Bano, S. Naiyer, S. Sanyal +2
    bioRxivPreprintAll rights reservedFull textMolecular biology & gene regulationbioRxiv
  4. Differential isoform-specific control of KCC2 function in developing and mature cortical neurons
    Carla Pagan, Pauline Weinzettl, Marika A Markkanen +3
    EMBO ReportsPeer-reviewedCC BYFull textMolecular biology & gene regulationDOAJ
  5. Lineage-specific and gestational age–dependent DNA methylation programming orchestrates human placental development
    Shanru Yi, Jing Xiao, Ruixue Wang +12
    Science AdvancesPeer-reviewedCC BY-NCFull textMolecular biology & gene regulationCrossrefEurope PMC
BibTeX
@misc{frayssinhes2026lineagespecific,
  title = {{Lineage-specific regulation and RNA-associated functions of SATB1 in mature B-cells}},
  author = {Jean-Yves Alejandro Frayssinhes and Lya Meriot and Tiffany Marchiol and Emilie Pinault and Thierry Forné and Charalampos Spilianakis and Eric Pinaud and Sandrine Le Noir},
  howpublished = {HAL},
  year = {2026},
  month = jul,
  doi = {10.64898/2026.07.22.739998},
  url = {https://hal.science/hal-05802449v1},
  note = {CC BY-NC-ND 4.0},
}
RIS
TY  - UNPB
TI  - Lineage-specific regulation and RNA-associated functions of SATB1 in mature B-cells
AU  - Jean-Yves Alejandro Frayssinhes
AU  - Lya Meriot
AU  - Tiffany Marchiol
AU  - Emilie Pinault
AU  - Thierry Forné
AU  - Charalampos Spilianakis
AU  - Eric Pinaud
AU  - Sandrine Le Noir
PY  - 2026
DA  - 2026/07/24
PB  - HAL
DO  - 10.64898/2026.07.22.739998
UR  - https://hal.science/hal-05802449v1
AB  - Special AT-rich binding protein 1 (SATB1) is a nuclear matrix-associated transcription factor that orchestrates higher-order chromatin architecture and gene expression in T and B lymphocytes. While SATB1’s role in T cells is well-established, its regulation and function in B cells remain underexplored. Here, we showed that Satb1 expression in mature B cells is controlled by alternative promoter usage and splicing, with promoters P1 and P3 dynamically switching upon LPS-induced activation, while P2 remains transcriptionally silent. We identified four Satb1 mRNA isoforms, including two novel transcripts ( Δ9 and Δ9Δ11 ), all of which maintain open reading frames. Satb1 transcription decreases upon activation while SATB1 protein content evolves differently, suggesting post-transcriptional regulation. SATB1 forms a high-molecular-weight complex in B cells, and co-immunoprecipitation mass spectrometry reveals RNA-binding proteins as its predominant interactors. These findings specify SATB1 expression kinetics during B-cell activation and reveal its role as a regulator of RNA splicing in B cells.
ER  -