Novel heterozygous SPI1c.538C>T p.(Leu180Phe) variant causes PU.1 haploinsufficiency leading to agammaglobulinemia

PU.1 is an Ets family transcription factor crucial for hematopoietic cell fate. Complete PU.1 deficiency lethally arrests lympho- and myelopoiesis in mice. Individuals with SPI1 heterozygous loss-of-function variants exhibit disrupted gene expression patterns associated with B cell development. We identified the vertical transmission of a heterozygous SPI1c.538C>T p.(L180F) variant in a Finnish family. The index patient and his mother had severe bacterial infections, agammaglobulinemia, and low myeloid and plasmacytoid dendritic cell counts. The variant carrier sister had slightly reduced B cell counts, isolated IgA deficiency, and reduced dendritic cell counts. All individuals had diminished PU.1 protein expression in monocytes. In vitro studies showed that PU.1 L180F variant is less expressed and predominantly located in the cytoplasm. PU.1 WT mainly interacts with chromatin and centrosome-associated proteins, while the L180F variant showed fewer interactions. Our findings describe a novel PU.1 variant leading to agammaglobulinemia with variable penetrance.

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Publication Details

Journal
Clinical Immunology
Published
2025-04-26
DOI
https://doi.org/10.1016/j.clim.2025.110503
Citations
3
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
2.39
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article

Novel heterozygous SPI1c.538C>T p.(Leu180Phe) variant causes PU.1 haploinsufficiency leading to agammaglobulinemia

Tanja Turunen, Timi Martelius, Titus J. Boggon, Ainsley V. C. Knox et al.
3 citations
Clinical Immunology
Immunodeficiency and Autoimmune Disorders
2.39
article

Novel heterozygous SPI1c.538C>T p.(Leu180Phe) variant causes PU.1 haploinsufficiency leading to agammaglobulinemia

Tanja Turunen, Timi Martelius, Titus J. Boggon, Ainsley V. C. Knox, Iftekhar Chowdhury, Ravindra Daddali, K Kettunen, Juha Grönholm, Nanni Mamia, Pia Laine, Neil Romberg, Markku Varjosalo, Mikko Seppänen, Amy L. Stiegler, Juha Kere, Markku Vänttinen
article en
3 citations

Abstract

PU.1 is an Ets family transcription factor crucial for hematopoietic cell fate. Complete PU.1 deficiency lethally arrests lympho- and myelopoiesis in mice. Individuals with SPI1 heterozygous loss-of-function variants exhibit disrupted gene expression patterns associated with B cell development. We identified the vertical transmission of a heterozygous SPI1c.538C>T p.(L180F) variant in a Finnish family. The index patient and his mother had severe bacterial infections, agammaglobulinemia, and low myeloid and plasmacytoid dendritic cell counts. The variant carrier sister had slightly reduced B cell counts, isolated IgA deficiency, and reduced dendritic cell counts. All individuals had diminished PU.1 protein expression in monocytes. In vitro studies showed that PU.1 L180F variant is less expressed and predominantly located in the cytoplasm. PU.1 WT mainly interacts with chromatin and centrosome-associated proteins, while the L180F variant showed fewer interactions. Our findings describe a novel PU.1 variant leading to agammaglobulinemia with variable penetrance.

Clinical ImmunologyVol. 277
Children's Hospital of Philadelphia (US), University of Helsinki (FI), Helsinki University Hospital (FI), Yale University (US), Kuopio University Hospital (FI), Folkhälsans Forskningscentrum (FI), Hospital District of Helsinki and Uusimaa (FI)
Zero hunger
Openalex Percentile: Top 12%
Immunodeficiency and Autoimmune Disorders
2.39
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