ZFIN ID: ZDB-PUB-171004-3
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features
Carapito, R., Konantz, M., Paillard, C., Miao, Z., Pichot, A., Leduc, M.S., Yang, Y., Bergstrom, K.L., Mahoney, D.H., Shardy, D.L., Alsaleh, G., Naegely, L., Kolmer, A., Paul, N., Hanauer, A., Rolli, V., Müller, J.S., Alghisi, E., Sauteur, L., Macquin, C., Morlon, A., Sancho, C.S., Amati-Bonneau, P., Procaccio, V., Mosca-Boidron, A.L., Marle, N., Osmani, N., Lefebvre, O., Goetz, J.G., Unal, S., Akarsu, N.A., Radosavljevic, M., Chenard, M.P., Rialland, F., Grain, A., Béné, M.C., Eveillard, M., Vincent, M., Guy, J., Faivre, L., Thauvin-Robinet, C., Thevenon, J., Myers, K., Fleming, M.D., Shimamura, A., Bottollier-Lemallaz, E., Westhof, E., Lengerke, C., Isidor, B., Bahram, S.
Date: 2017
Source: The Journal of Clinical Investigation   127(11): 4090-4103 (Journal)
Registered Authors: Alghisi, Elisa, Konantz, Martina, Lengerke, Claudia, Morlon, Aurore, Müller, Joëlle, Sauteur, Loïc
Keywords: none
MeSH Terms:
  • Animals
  • Bone Marrow Diseases/genetics*
  • Child
  • DNA Mutational Analysis
  • Exocrine Pancreatic Insufficiency/genetics*
  • Female
  • Genetic Association Studies
  • Humans
  • Infant
  • Lipomatosis/genetics*
  • Male
  • Models, Molecular
  • Neutropenia/congenital*
  • Neutropenia/genetics
  • Pancreas, Exocrine/metabolism
  • Phenotype
  • Protein Domains
  • Signal Recognition Particle/chemistry
  • Signal Recognition Particle/genetics*
  • Zebrafish
PubMed: 28972538 Full text @ Journal of Clin. Invest.
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.