New pathogenic mechanisms induced by germline erythropoietin receptor mutations in primary erythrocytosis.
(2017) Haematologica : the hematology journal — (2017)
Files
103PasquieretalHaematologica2017.pdf
Open Access - Adobe PDF
- 1.08 MB
Details
- Authors
Balligand, Thomas 
- Abstract
- Primary Familial and Congenital Polycythemia is characterized by erythropoietin hypersensitivity of erythroid progenitors due to germline nonsense or frameshift mutations in the erythropoietin receptor gene. All mutations already described lead to the truncation of the C-terminal receptor sequence that contains negative regulatory domains. Their removal is presented as sufficient to cause the erythropoietin hypersensitivity phenotype. Here, we provide evidence for a new mechanism whereby the presence of novel sequences generated by frameshift mutations are required for the phenotype rather than just extensive truncation resulting from nonsense mutations. We show that the erythropoietin hypersensitivity induced by a new erythropoietin receptor mutant, p.Gln434Profs*11, could not be explained by the loss of negative signaling and of the internalization domains, but rather by the appearance of a new C-terminal tail. The latter, by increasing erythropoietin receptor dimerization, stability and cell-surface localization causes pre-activation of erythropoietin receptor and JAK2, constitutive signaling and hypersensitivity to erythropoietin. Similar results were obtained with another mutant, p.Pro438Metfs*6, that shares the same last 5 amino acid residues (MDTVP) with erythropoietin receptor p.Gln434Profs*11, confirming the involvement of the new peptidic sequence in the erythropoietin hypersensitivity phenotype. These results suggest a new mechanism that might be common to erythropoietin receptor frameshift mutations. In summary, we show that Primary Familial and Congenital Polycythemia is more complex than expected since distinct mechanisms are involved in the erythropoietin hypersensitivity phenotype, according to the type of erythropoietin receptor mutation.
- Affiliations
Citations
Pasquier, F., Marty, C., Balligand, T., Verdier, F., Grosjean, S., Gryshkova, V., Raslova, H., Constantinescu, S., Casadevall, N., Vainchenker, W., Bellanné-Chantelot, C., & Plo, I. (2017). New pathogenic mechanisms induced by germline erythropoietin receptor mutations in primary erythrocytosis. Haematologica : the hematology journal. Published. https://doi.org/10.3324/haematol.2017.176370 (Original work published 2017)