Control of Growth Within Drosophila Peripheral Nerves by Ras and Protein Kinase A

Abstract

The long term goals of this research are to understand the mechanisms by which NF1 and its partners control growth using the Drosophila peripheral nerve as our assay system. This system is advantageous because we can apply a number of powerful molecular genetic methodologies that are not available in other systems. For task #3, we used RNA interference to generate preliminary evidence that push acts in the peripheral glia to control perineurial glial growth. This preliminary finding will be pursued in much greater detail during the next funding period. Our major findings continue to be generated from aim #4. Our finding, reported last year, that Ras nonautonomously activates perineurial glial growth via PI3 Kinase, Akt and FOXO, was published in the Journal of Neuroscience. During this funding period we found evidence for a role for the Akt-regulated Tor pathway in regulating glial growth: for example, expression of a dominant-negative S6 kinase suppressed the increased glial growth conferred by PI3K-CAAX. This and other observations raise the possibility that Tor and FOXO interact to control glial growth. We also report evidence that the Ras-activated Ral GTPase participates with PI3K inglial growth control.

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Document Details

Document Type
Technical Report
Publication Date
Feb 01, 2007
Accession Number
ADA515523

Entities

People

  • Michael Stern

Organizations

  • Rice University

Tags

Communities of Interest

  • Air Platforms
  • Biomedical

DTIC Thesaurus Topics

  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Diptera
  • Genetics
  • Growth Factors
  • Neoplasms
  • Neuroglia
  • Neuromuscular Diseases
  • Neurosciences
  • Observation
  • Peptide Growth Factors
  • Peptides
  • Peripheral Nervous System
  • Proteins
  • Transcription Factors

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics
  • Neuroscience

Technology Areas

  • Biotechnology