Back to Search Start Over

Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice.

Authors :
Kon A
Yamazaki S
Nannya Y
Kataoka K
Ota Y
Nakagawa MM
Yoshida K
Shiozawa Y
Morita M
Yoshizato T
Sanada M
Nakayama M
Koseki H
Nakauchi H
Ogawa S
Source :
Blood [Blood] 2018 Feb 08; Vol. 131 (6), pp. 621-635. Date of Electronic Publication: 2017 Nov 16.
Publication Year :
2018

Abstract

Splicing factor mutations are characteristic of myelodysplastic syndromes (MDS) and related myeloid neoplasms and implicated in their pathogenesis, but their roles in the development of MDS have not been fully elucidated. In the present study, we investigated the consequence of mutant Srsf2 expression using newly generated Vav1-Cre -mediated conditional knockin mice. Mice carrying a heterozygous Srsf2 P95H mutation showed significantly reduced numbers of hematopoietic stem and progenitor cells (HSPCs) and differentiation defects both in the steady-state condition and transplantation settings. Srsf2 -mutated hematopoietic stem cells (HSCs) showed impaired long-term reconstitution compared with control mice in competitive repopulation assays. Although the Srsf2 mutant mice did not develop MDS under the steady-state condition, when their stem cells were transplanted into lethally irradiated mice, the recipients developed anemia, leukopenia, and erythroid dysplasia, which suggests the role of replicative stress in the development of an MDS-like phenotype in Srsf2 -mutated mice. RNA sequencing of the Srsf2 -mutated HSPCs revealed a number of abnormal splicing events and differentially expressed genes, including several potential targets implicated in the pathogenesis of hematopoietic malignancies, such as Csf3r , Fyn , Gnas , Nsd1 , Hnrnpa2b1 , and Trp53bp1 Among the mutant Srsf2 -associated splicing events, most commonly observed were the enhanced inclusion and/or exclusion of cassette exons, which were caused by the altered consensus motifs for the recognition of exonic splicing enhancers. Our findings suggest that the mutant Srsf2 leads to a compromised HSC function by causing abnormal RNA splicing and expression, contributing to the deregulated hematopoiesis that recapitulates the MDS phenotypes, possibly as a result of additional genetic and/or environmental insults.<br /> (© 2018 by The American Society of Hematology.)

Details

Language :
English
ISSN :
1528-0020
Volume :
131
Issue :
6
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
29146882
Full Text :
https://doi.org/10.1182/blood-2017-01-762393