PUBLICATION
SRP54 mutations induce Congenital Neutropenia via dominant-negative effects on XBP1 splicing
- Authors
- Schürch, C., Schaefer, T., Müller, J.S., Hanns, P., Arnone, M., Dumlin, A., Schärer, J., Sinning, I., Wild, K., Skokowa, J., Welte, K., Carapito, R., Bahram, S., Konantz, M., Lengerke, C.
- ID
- ZDB-PUB-201124-9
- Date
- 2020
- Source
- Blood 137(10): 1340-1352 (Journal)
- Registered Authors
- Hanns, Pauline, Konantz, Martina, Lengerke, Claudia, Schürch, Christoph
- Keywords
- none
- MeSH Terms
-
- Animals
- Congenital Bone Marrow Failure Syndromes/genetics*
- Disease Models, Animal
- Gene Deletion
- Gene Expression Regulation, Developmental
- Gene Knockout Techniques
- HL-60 Cells
- Humans
- Models, Molecular
- Mutation
- Neutropenia/congenital*
- Neutropenia/genetics
- RNA Splicing
- RNA, Messenger/genetics
- Signal Recognition Particle/genetics*
- X-Box Binding Protein 1/genetics*
- Zebrafish/genetics*
- Zebrafish Proteins/genetics*
- PubMed
- 33227812 Full text @ Blood
Citation
Schürch, C., Schaefer, T., Müller, J.S., Hanns, P., Arnone, M., Dumlin, A., Schärer, J., Sinning, I., Wild, K., Skokowa, J., Welte, K., Carapito, R., Bahram, S., Konantz, M., Lengerke, C. (2020) SRP54 mutations induce Congenital Neutropenia via dominant-negative effects on XBP1 splicing. Blood. 137(10):1340-1352.
Abstract
Heterozygous de novo missense variants of SRP54 were recently identified in patients with congenital neutropenia (CN), displaying symptoms overlapping with Shwachman-Diamond-Syndrome (SDS).1 Here, we investigate srp54 KO zebrafish as the first in vivo model of SRP54 deficiency. srp54-/- zebrafish are embryonically lethal and display, next to severe neutropenia, multi-systemic developmental defects. In contrast, srp54+/- zebrafish are viable, fertile and only show mild neutropenia. Interestingly, injection of human SRP54 mRNAs carrying mutations observed in patients (T115A, T117Δ and G226E) aggravated neutropenia and induced pancreatic defects in srp54+/- fish, mimicking the corresponding human clinical phenotypes. These data suggest that the variable phenotypes observed in patients may be due to mutation-specific dominant negative effects on the functionality of the residual wildtype SRP54 protein. Consistently, overexpression of mutated SRP54 also induced neutropenia in wildtype fish and impaired granulocytic maturation of human promyelocytic HL-60 cells as well as of healthy cord-blood derived CD34+ HSPCs. Mechanistically, srp54 mutant fish and human cells show impaired unconventional splicing of the transcription factor X-box binding protein 1 (Xbp1). Vice-versa, xbp1 morphants recapitulate phenotypes observed in srp54 deficiency and, importantly, injection of spliced, but not unspliced xbp1 mRNA rescues neutropenia in srp54+/- zebrafish. Together, these data indicate that SRP54 is critical for the development of various tissues, with neutrophils reacting most sensitively to SRP54 loss. The heterogenic phenotypes observed in patients, ranging from mild CN to SDS-like disease, may be due to different dominant negative effects of mutated SRP54 proteins on downstream XBP1 splicing, which represents a potential therapeutic target.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping