Role of novel genes myelopoiesis

Information

  • Research Project
  • 7713855
  • ApplicationId
    7713855
  • Core Project Number
    K01DK069672
  • Full Project Number
    7K01DK069672-05
  • Serial Number
    69672
  • FOA Number
    PAR-02-065
  • Sub Project Id
  • Project Start Date
    2/1/2005 - 20 years ago
  • Project End Date
    11/30/2009 - 15 years ago
  • Program Officer Name
    BISHOP, TERRY ROGERS
  • Budget Start Date
    2/1/2008 - 17 years ago
  • Budget End Date
    12/31/2008 - 16 years ago
  • Fiscal Year
    2008
  • Support Year
    5
  • Suffix
  • Award Notice Date
    11/3/2008 - 16 years ago

Role of novel genes myelopoiesis

DESCRIPTION (provided by applicant): This proposal is designed to provide the candidate a period of mentored research in the laboratory of Dr. A. T. Look, a pioneer in the field of zebrafish neoplasias and myeloid development. Dr. Look's clinical and research expertise, collaborations, and resources will assist the candidate in developing the skills and autonomy required to become a successful independent investigator. In addition, an advisory committee of highly regarded scientists will provide scientific and career advice. The goal of this application is to use the zebrafish as a model to study novel genes and pathways necessary for myeloid development that can subsequently be examined for similar roles in mammalian systems. Mammalian hematopoiesis is a multistep process involving the progressive commitment of pluripotent hematopoietic stem cells into the wide variety of terminally differentiated cells of the blood system. The successive waves of tissue specification are regulated by specific patterns of gene expression. In zebrafish, most mature blood cell types and key transcription factors are conserved, suggesting that the regulatory mechanisms directing lineage specification are similarly conserved. To identify novel genes involved in myeloid development, the candidate has analyzed a panel of zebrafish insertional mutants, provided by Dr. Nancy Hopkins at MIT, and identified mutants with deficient or abnormal distribution of myeloperoxidase, a gene specifically expressed in zebrafish granulocytes. This proposal will focus on mutants of the transcription factor supt6h, ubiquitin ligase F-Box 5 (fbxo5), Na/K ATPase (atp1a1), or Replication Protein A (rpa1) genes. The central hypothesis of this work is that these genes will have critical roles in normal myeloid development. To address this hypothesis, the hematopoietic phenotypes of the mutants will be analyzed and the role of individual genes in myeloid development will be examined. The analysis of these mutants will establish the basis for future studies in myeloid development and malignancies by this candidate.

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    K01
  • Administering IC
    DK
  • Application Type
    7
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    120315
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    847
  • Ed Inst. Type
  • Funding ICs
    NIDDK:120315\
  • Funding Mechanism
  • Study Section
    DDK
  • Study Section Name
    Diabetes and Digestive and Kidney Diseases Special Grants Review Committee
  • Organization Name
    INSTITUTE FOR CANCER RESEARCH
  • Organization Department
  • Organization DUNS
    872612445
  • Organization City
    Philadelphia
  • Organization State
    PA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    191112434
  • Organization District
    UNITED STATES