Accession Number : AD1007018


Title :   Signaling Pathways in Pathogenesis of Diamond Blackfan Anemia


Descriptive Note : Technical Report,30 Sep 2012,29 Sep 2015


Corporate Author : Stanford University Stanford United States


Personal Author(s) : Sakamoto,Kathleen M


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/1007018.pdf


Report Date : 01 Dec 2015


Pagination or Media Count : 14


Abstract : Diamond Blackfan Anemia (DBA) is a disorder that results in pure red cell aplasia, congenital abnormalities, and predisposition to cancer. The current treatment of steroids and chronic transfusions leads to significant morbidity. Approximately 25 percent of patients with DBA have mutations in RPS19. We previously generated a zebrafish model with RPS19 insufficiency that the phenotype is similar to that observed in patients with DBA. We also first described that p53 is upregulated in these fish injected with RPS19 morpholinos. To understand the mechanism by which RPS19 insufficiency leads to defects in erythropoiesis, we identified a p53 target, microRNA34a (miR34a), as being upregulated in human CD34 positive fetal liver cells transduced with RPS19shRNA lentivirus. This not only led to decreased erythroid colony formation, but also aberrant erythroid differentiation. We hypothesize that RPS19 insufficiency mediates defects in erythropoiesis through upregulation of p53 and miR34a. To more rigorously test this hypothesis and identify new downstream targets and microRNAs, we propose three specific aims. In Aim 1, we will characterize the role of miR34a in RPS19 insufficient primary human hematopoietic stem cells in vitro. In Aim 2, we will study the role of miR34a in RPS19 insufficient primary human hematopoietic stem cells in vivo. In Aim 3, RNA-seq will be performed to identify novel transcripts and microRNAs that are aberrantly regulated downstream of RPS19 insufficiency in primary human hematopoietic stem cells.


Descriptors :   ANEMIAS , stem cells , RIBONUCLEIC ACIDS , THERAPY


Distribution Statement : APPROVED FOR PUBLIC RELEASE