Unknown

Dataset Information

0

A Forward Genetic Screen Targeting the Endothelium Reveals a Regulatory Role for the Lipid Kinase Pi4ka in Myelo- and Erythropoiesis.


ABSTRACT: Given its role as the source of definitive hematopoietic cells, we sought to determine whether mutations initiated in the hemogenic endothelium would yield hematopoietic abnormalities or malignancies. Here, we find that endothelium-specific transposon mutagenesis in mice promotes hematopoietic pathologies that are both myeloid and lymphoid in nature. Frequently mutated genes included previously recognized cancer drivers and additional candidates, such as Pi4ka, a lipid kinase whose mutation was found to promote myeloid and erythroid dysfunction. Subsequent validation experiments showed that targeted inactivation of the Pi4ka catalytic domain or reduction in mRNA expression inhibited myeloid and erythroid cell differentiation in vitro and promoted anemia in vivo through a mechanism involving deregulation of AKT, MAPK, SRC, and JAK-STAT signaling. Finally, we provide evidence linking PI4KAP2, previously considered a pseudogene, to human myeloid and erythroid leukemia.

SUBMITTER: Ziyad S 

PROVIDER: S-EPMC5828030 | biostudies-literature | 2018 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

A Forward Genetic Screen Targeting the Endothelium Reveals a Regulatory Role for the Lipid Kinase Pi4ka in Myelo- and Erythropoiesis.

Ziyad Safiyyah S   Riordan Jesse D JD   Cavanaugh Ann M AM   Su Trent T   Hernandez Gloria E GE   Hilfenhaus Georg G   Morselli Marco M   Huynh Kristine K   Wang Kevin K   Chen Jau-Nian JN   Dupuy Adam J AJ   Iruela-Arispe M Luisa ML  

Cell reports 20180101 5


Given its role as the source of definitive hematopoietic cells, we sought to determine whether mutations initiated in the hemogenic endothelium would yield hematopoietic abnormalities or malignancies. Here, we find that endothelium-specific transposon mutagenesis in mice promotes hematopoietic pathologies that are both myeloid and lymphoid in nature. Frequently mutated genes included previously recognized cancer drivers and additional candidates, such as Pi4ka, a lipid kinase whose mutation was  ...[more]

Similar Datasets

2018-01-30 | GSE108355 | GEO
2018-01-30 | GSE108354 | GEO
2018-01-30 | GSE108353 | GEO
| PRJNA423251 | ENA
| PRJNA423253 | ENA
| PRJNA423258 | ENA
| S-EPMC5909886 | biostudies-literature
| S-EPMC3510250 | biostudies-literature
| S-EPMC7969590 | biostudies-literature
| S-EPMC9576605 | biostudies-literature