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Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features
Raphael Carapito, et al.
Raphael Carapito, et al.
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Research Article Genetics Hematology

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features

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Abstract

Shwachman-Diamond syndrome (SDS) (OMIM #260400) is a rare inherited bone marrow failure syndrome (IBMFS) that is primarily characterized by neutropenia and exocrine pancreatic insufficiency. Seventy-five to ninety percent of patients have compound heterozygous loss-of-function mutations in the Shwachman-Bodian-Diamond syndrome (sbds) gene. Using trio whole-exome sequencing (WES) in an sbds-negative SDS family and candidate gene sequencing in additional SBDS-negative SDS cases or molecularly undiagnosed IBMFS cases, we identified 3 independent patients, each of whom carried a de novo missense variant in srp54 (encoding signal recognition particle 54 kDa). These 3 patients shared congenital neutropenia linked with various other SDS phenotypes. 3D protein modeling revealed that the 3 variants affect highly conserved amino acids within the GTPase domain of the protein that are critical for GTP and receptor binding. Indeed, we observed that the GTPase activity of the mutated proteins was impaired. The level of SRP54 mRNA in the bone marrow was 3.6-fold lower in patients with SRP54-mutations than in healthy controls. Profound reductions in neutrophil counts and chemotaxis as well as a diminished exocrine pancreas size in a SRP54-knockdown zebrafish model faithfully recapitulated the human phenotype. In conclusion, autosomal dominant mutations in SRP54, a key member of the cotranslation protein-targeting pathway, lead to syndromic neutropenia with a Shwachman-Diamond–like phenotype.

Authors

Raphael Carapito, Martina Konantz, Catherine Paillard, Zhichao Miao, Angélique Pichot, Magalie S. Leduc, Yaping Yang, Katie L. Bergstrom, Donald H. Mahoney, Deborah L. Shardy, Ghada Alsaleh, Lydie Naegely, Aline Kolmer, Nicodème Paul, Antoine Hanauer, Véronique Rolli, Joëlle S. Müller, Elisa Alghisi, Loïc Sauteur, Cécile Macquin, Aurore Morlon, Consuelo Sebastia Sancho, Patrizia Amati-Bonneau, Vincent Procaccio, Anne-Laure Mosca-Boidron, Nathalie Marle, Naël Osmani, Olivier Lefebvre, Jacky G. Goetz, Sule Unal, Nurten A. Akarsu, Mirjana Radosavljevic, Marie-Pierre Chenard, Fanny Rialland, Audrey Grain, Marie-Christine Béné, Marion Eveillard, Marie Vincent, Julien Guy, Laurence Faivre, Christel Thauvin-Robinet, Julien Thevenon, Kasiani Myers, Mark D. Fleming, Akiko Shimamura, Elodie Bottollier-Lemallaz, Eric Westhof, Claudia Lengerke, Bertrand Isidor, Seiamak Bahram

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Figure 6

Effects of srp54 gene knockdown on pancreas development in zebrafish embryos.

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Effects of srp54 gene knockdown on pancreas development in zebrafish emb...
(A) Confocal images of control-injected, MO-injected, and MO plus 100 pg hSRP54 mRNA–injected transgenic Tg(ptf1a:Gal4 UAS:Kaede) embryos at 72 hpf. Lateral views are shown, with anterior to the left, dorsal up. Arrows indicate downregulation (↓) or rescued expression (↑) for each gene. The red boxed area corresponds to 300 µm (confocal images were taken with a ×10 objective). Original magnification, ×3, for the images below, which show enlarged views of the red boxed area. (B) WISH of insa at 72 hpf in control-injected, MO-injected and MO plus 100 pg hSRP54 mRNA–injected embryos. Dorsal views are shown, with anterior to the left. Shown are representative images from 3 biological replicate experiments with 4 or more embryos per group for each individual biological replicate experiment. Embryo size depicted: 1.75 mm (whole embryo size is 3.5 mm); original magnification of insets, ×2 (images were taken with a ×5 objective on a Leica DM 2000 LED microscope). The graphs below each panel in A and B display the percentages of embryos with normal versus decreased expression in all embryos analyzed across the biological replicates. Numbers indicate the amount of embryos with the respective phenotype/total number of embryos analyzed. ***P < 0.001, by Fisher’s exact test.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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