Detail of 081505_L1



Project
Title
BDML file for quantitative information about nuclear division dynamics of wild-type embryo
Description
NA
Release, Updated
2013-10-03,
2018-11-15
License
CC BY-NC-SA
Kind
Quantitative data based on Experiment
File Formats
Data size
22.9 MB

Organism
C. elegans ( NCBITaxon:6239 )
Strain(s)
-
Cell Line
-

Datatype
nuclear division dynamics
Molecular Function (MF)
Biological Process (BP)
embryo development ( GO:0009790 )
Cellular Component (CC)
nucleus ( GO:0005634 )
Biological Imaging Method
XYZ Scale
XY: 0.09 micrometer/pixel, Z: 1.0 micrometer/slice
T scale
1.0 minute for each time interval

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
Fluorescence
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
See details in Bao et al. (2006) Proc. Natl. Acad. Sci. U.S.A., 103(8): 2707-2712.
Related paper(s)

Zhirong Bao, John I Murray, Thomas Boyle, Siew Loon Ooi, Matthew J Sandel, Robert H Waterston (2006) Automated cell lineage tracing in Caenorhabditis elegans., Proceedings of the National Academy of Sciences of the United States of America, Volume 103, Number 8, pp. 2707-12

Published in 2006 Feb 21 (Electronic publication in Feb. 13, 2006, midnight )

(Abstract) The invariant cell lineage and cell fate of Caenorhabditis elegans provide a unique opportunity to decode the molecular mechanisms of animal development. To exploit this opportunity, we have developed a system for automated cell lineage tracing during C. elegans embryogenesis, based on 3D, time-lapse imaging and automated image analysis. Using ubiquitously expressed histone-GFP fusion protein to label cells/nuclei and a confocal microscope, the imaging protocol captures embryogenesis at high spatial (31 planes at 1 microm apart) and temporal (every minute) resolution without apparent effects on development. A set of image analysis algorithms then automatically recognizes cells at each time point, tracks cell movements, divisions and deaths over time and assigns cell identities based on the canonical naming scheme. Starting from the four-cell stage (or earlier), our software, named starrynite, can trace the lineage up to the 350-cell stage in 25 min on a desktop computer. The few errors of automated lineaging can then be corrected in a few hours with a graphic interface that allows easy navigation of the images and the reported lineage tree. The system can be used to characterize lineage phenotypes of genes and/or extended to determine gene expression patterns in a living embryo at the single-cell level. We envision that this automation will make it practical to systematically decipher the developmental genes and pathways encoded in the genome of C. elegans.
(MeSH Terms)

Contact
Robert H. Waterston , University of Washington , Department of Genome Sciences
Contributors
Zhirong Bao, John I. Murray, Thomas Boyle, Siew Loon Ooi, Matthew J. Sandel, Robert H. Waterston

Local ID
081505_L1
BDML ID
aeabe0e1-bcc3-4948-acb7-7c6736949404
BDML/BD5
Workflow