## Abstract Human lymphocytes gene expression is monitored before and after PHA stimulation over 72 h, using DNA microarray technology. Results are then compared with our previous bioinformatics predictions, which identified six leader genes of highest importance in human T lymphocytes cell cycle.
Gene profiling and bioinformatic analysis of Schwann cell embryonic development and myelination
✍ Scribed by Maurizio D'antonio; David Michalovich; Morris Paterson; Anna Droggiti; Ashwin Woodhoo; Rhona Mirsky; Kristjan R. Jessen
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 690 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
To elucidate the molecular mechanisms involved in Schwann cell development, we profiled gene expression in the developing and injured rat sciatic nerve. The genes that showed significant changes in expression in developing and dedifferentiated nerve were validated with RT‐PCR, in situ hybridisation, Western blot and immunofluorescence. A comprehensive approach to annotating micro‐array probes and their associated transcripts was performed using Biopendium™, a database of sequence and structural annotation. This approach significantly increased the number of genes for which a functional insight could be found. The analysis implicates agrin and two members of the collapsin response‐mediated protein (CRMP) family in the switch from precursors to Schwann cells, and synuclein‐1 and αB‐crystallin in peripheral nerve myelination. We also identified a group of genes typically related to chondrogenesis and cartilage/bone development, including type II collagen, that were expressed in a manner similar to that of myelin‐associated genes. The comprehensive function annotation also identified, among the genes regulated during nerve development or after nerve injury, proteins belonging to high‐interest families, such as cytokines and kinases, and should therefore provide a uniquely valuable resource for future research. © 2005 Wiley‐Liss, Inc.
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