TY - JOUR
T1 - Whole-animal imaging, gene function, and the Zebrafish Phenome Project
AU - Cheng, Keith C.
AU - Xin, Xuying
AU - Clark, Darin P.
AU - La Riviere, Patrick
N1 - Funding Information:
We acknowledge funding from NIH ( R24RR017441 , R01CA242956 , and R01AR052535 to KC and RO1CA13468 to PLR). We also acknowledge encouragement and advice from Stephen Phillips (emeritus, Jefferson U), help with imaging on the Skyscan 1172 from Tim Sledz and Arun Tatiparthi of Micro Photonics (Allentown, PA), the work of Jean Copper and Steve Peckins in the Cheng lab, and discussions with G. Kindlmann at U Chicago, F. De Carlo and X Xiao of the Advanced Photon Source at the Argonne National Laboratory in Illinois, Sean Megason at Harvard, and Raghu Machiraju at Ohio State.
PY - 2011/10
Y1 - 2011/10
N2 - Imaging can potentially make a major contribution to the Zebrafish Phenome Project, which will probe the functions of vertebrate genes through the generation and phenotyping of mutants. Imaging of whole animals at different developmental stages through adulthood will be used to infer biological function. Cell resolutions will be required to identify cellular mechanism and to detect a full range of organ effects. Light-based imaging of live zebrafish embryos is practical only up to ~2 days of development, owing to increasing pigmentation and diminishing tissue lucency with age. The small size of the zebrafish makes possible whole-animal imaging at cell resolutions by histology and micron-scale tomography (microCT). The histological study of larvae is facilitated by the use of arrays, and histology's standard use in the study of human disease enhances its translational value. Synchrotron microCT with X-rays of moderate energy (10-25. keV) is unimpeded by pigmentation or the tissue thicknesses encountered in zebrafish of larval stages and beyond, and is well-suited to detecting phenotypes that may require 3D modeling. The throughput required for this project will require robotic sample preparation and loading, increases in the dimensions and sensitivity of scintillator and CCD chips, increases in computer power, and the development of new approaches to image processing, segmentation, and quantification.
AB - Imaging can potentially make a major contribution to the Zebrafish Phenome Project, which will probe the functions of vertebrate genes through the generation and phenotyping of mutants. Imaging of whole animals at different developmental stages through adulthood will be used to infer biological function. Cell resolutions will be required to identify cellular mechanism and to detect a full range of organ effects. Light-based imaging of live zebrafish embryos is practical only up to ~2 days of development, owing to increasing pigmentation and diminishing tissue lucency with age. The small size of the zebrafish makes possible whole-animal imaging at cell resolutions by histology and micron-scale tomography (microCT). The histological study of larvae is facilitated by the use of arrays, and histology's standard use in the study of human disease enhances its translational value. Synchrotron microCT with X-rays of moderate energy (10-25. keV) is unimpeded by pigmentation or the tissue thicknesses encountered in zebrafish of larval stages and beyond, and is well-suited to detecting phenotypes that may require 3D modeling. The throughput required for this project will require robotic sample preparation and loading, increases in the dimensions and sensitivity of scintillator and CCD chips, increases in computer power, and the development of new approaches to image processing, segmentation, and quantification.
UR - http://www.scopus.com/inward/record.url?scp=82455212137&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=82455212137&partnerID=8YFLogxK
U2 - 10.1016/j.gde.2011.08.006
DO - 10.1016/j.gde.2011.08.006
M3 - Review article
C2 - 21963132
AN - SCOPUS:82455212137
SN - 0959-437X
VL - 21
SP - 620
EP - 629
JO - Current Opinion in Genetics and Development
JF - Current Opinion in Genetics and Development
IS - 5
ER -