2016 Xenopus White Paper
Dear Xenopus Community,
The 2016 Xenopus Community White Paper is finished as prepared by Sally Moody and Amy Sater.
Its contents are based on discussions from the 2015 PIs Meeting at Woods Hole:
Executive Summary:
Xenopus is an essential vertebrate model system for biomedical research
Past NIH investment in research using Xenopus has advanced biomedical research
Community recommendations for continued NIH investment in Xenopus research
Long term goals of using Xenopus for biomedical research
Xenopus is an essential vertebrate model sysytem for:
Understanding fundamental biological processes
Applying fundamental knowledge to pathological processes
Deciphering the function of human disease genes
Modeling human diseases
Recommendations for Continued NIH Investment in Xenopus Research:
Immediate Needs
Development of Protein Resources (ORFeome; Antibodies; Proteome)
Development of Big Data Repositories (Xenbase, XenMine)
Essential resources:
Enhancement of Efficient Gene Editing Approaches and Mutant Lines
Enhancement of Transgenic Resources
Improvement and Expansion of Amphibian Genomic Resources
Support for Xenopus Training and Meetings
Long Term Goal of Using Xenopus to Understand Human Disease
Download the 2016 Xenopus Community White Paper:
PIs: Please reference the White Paper in your NIH grant proposals and contact your program officers.
Authors:
Sally A. Moody
Amy K. Sater
Contributors:
Dominique Alfandari
Julie Baker
Ira Blitz
Ben Evans
Mike Gilchrist
Marko Horb
Aldo Ciau-Uitz
Darcy Kelley
Takuya Nakayama
Christine Reid
Jacques Robert
Todd Stukenberg
Martin Wuehr
Aaron Zorn
Xenopus is an essential vertebrate model system for biomedical research
Past NIH investment in research using Xenopus has advanced biomedical research
Community recommendations for continued NIH investment in Xenopus research
Long term goals of using Xenopus for biomedical research
Xenopus is an essential vertebrate model sysytem for:
Understanding fundamental biological processes
Applying fundamental knowledge to pathological processes
Deciphering the function of human disease genes
Modeling human diseases
Recommendations for Continued NIH Investment in Xenopus Research:
Immediate Needs
Development of Protein Resources (ORFeome; Antibodies; Proteome)
Development of Big Data Repositories (Xenbase, XenMine)
Essential resources:
Enhancement of Efficient Gene Editing Approaches and Mutant Lines
Enhancement of Transgenic Resources
Improvement and Expansion of Amphibian Genomic Resources
Support for Xenopus Training and Meetings
Long Term Goal of Using Xenopus to Understand Human Disease