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MicroRNAs and hematopoietic differentiation

$230,250R56FY2010DKNIH

Whitehead Institute For Biomedical Res, Cambridge MA

Investigators

Linked publications & trials

Abstract

DESCRIPTION (provided by applicant): MicroRNAs (miRNAs) are an abundant and highly conserved class of endogenous ~22-base RNAs that play crucial roles in cell function and development by base pairing to sites within target mRNAs, triggering either translational repression or mRNA degradation, or both. Our long-term goal is to discover the regulatory roles of several conserved miRNAs in critical and well-defined stages in formation of erythrocytes - uncovering not only their specific mRNA targets at both the BFU-E and CFU-E developmental stages but also the underlying network of miRNAs and their mRNA targets essential for these developmental transitions. Our specific aims are 1) to investigate the functions of miR-144, 451, 221, 222, and 223 in terminal proliferation and differentiation of CFU-E progenitors. We will determine the cellular effects on erythroid differentiation of ectopically overexpressing or knocking down expression these miRNAs in cultured CFU-E cells. Next we will determine the developmentally important mRNA targets downregulated by each of these miRNAs during specific stages of CFU-E proliferation and differentiation using a combination of experimental and computational approaches, and we will determine the roles of selected key miRNA target interactions during erythroid differentiation in culture. In Aim 2 we will use similar techniques to determine the functions of miR- 221, miR-222, miR-223 and other developmentally regulated miRNAs in the proliferation of BFU-E progenitors and the formation of CFU-Es. These studies will provide important information on the gene regulatory circuitry that controls hematopoiesis, and provide insights into pathological states caused by aberrant expression of certain miRNAs.

View original record on NIH RePORTER →