ADAM Functions in Early Development of Xenopus Tropicalis

Author:
Xu, Guofeng, Department of Cell Biology, University of Virginia
Advisors:
Desimone, Douglas W., Department of Cell Biology, University of Virginia
White, Judith, Department of Cell Biology, University of Virginia
Lu, Xiaowei, Department of Cell Biology, University of Virginia
Gumbiner, Barry, Department of Cell Biology, University of Virginia
Keller, Raymond, Department of Biology, University of Virginia
Abstract:

The ADAM family of transmembrane metalloproteinases has important functions in fertilization, development and disease. Previous studies suggest that ADAM10, a proteolytically active ADAM, plays essential roles in the development of primary neurons in both Drosophila and mouse. However, morpholino knockdown of ADAM10 in Xenopus failed to yield obvious defects in primary neurogenesis. In an attempt to investigate this apparent inconsistency, I identified a novel ADAM protein in Xenopus tropicalis (X. tropicalis) that is closely related to ADAM10. Homologues of this ADAM (which we named ADAM10-like) are present in several other vertebrate species, including some non-placental mammals. Morpholino knockdown ofADAM10-like caused early developmental delays in neurogenesis, as well as a bent-tail phenotype at later stages. Double knockdown ofADAM10 and ADAM10-like resulted in more severe defects in tail morphology but no obvious defects in neurogenesis other than a delay in timing. These results indicate that ADAM10-like has multiple functions during development, some of which are redundant with ADAM10.

Note: Abstract extracted from PDF file via OCR

Degree:
PHD (Doctor of Philosophy)
Language:
English
Rights:
All rights reserved (no additional license for public reuse)
Issued Date:
2012/05/01