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Series GSE25617 Query DataSets for GSE25617
Status Public on Dec 15, 2010
Title Molecular dissection of the migrating posterior lateral line primordium during early development in zebrafish
Organism Danio rerio
Experiment type Expression profiling by array
Summary The posterior lateral line system in zebrafish involves cell migration, proliferation and differentiation into mechanosensory cells. During development, a group of cranial placodal cells delaminate and become a coherent, migratory primordium that traverses the length of the fish to form this sensory system. As they migrate, the primordium deposits groups of cells called neuromasts, the specialized organs that contain the mechanosensory hair cells. The lateral line hair cells of fish are related to inner ear hair cells; therefore the primordium provides both a model for studying collective directional cell migration and the differentiation of sensory cells from multipotent progenitor cells. Through the combination of transgenic fish, Fluorescence Activated Cell Sorting and microarray analysis we identified a repertoire of key genes expressed in the migrating primordium and in differentiated neuromasts. We validated the specific expression in the primordium of a subset of the identified sequences by quantitative RT-PCR, and by in situ hybridization. We also show that interfering with the function of f11r and cd9b induces defects in its migratory behavior. Finally, pathway construction revealed functional relationships among the genes enriched in the migrating cell population. Our results demonstrate that this is a robust approach to globally analyze specific expression and we predict that many of the genes identified in this study will show critical functions in developmental and tumor progression process relating to posterior lateral line development.
 
Overall design The experiment was performed in two developmental stages, 36 and 48 hours post-fertilization. Two-condition experiment, GFP- (negative control) and GFP+ cells. Two biological repeats by stage, each by quadruplicate including a dye swap.
 
Contributor(s) Gallardo VE, Liang J, Behra M, Elkahloun A, Villablanca EJ, Russo V, Allende ML, Burgess SM
Citation(s) 21144052
Submission date Nov 26, 2010
Last update date Mar 22, 2012
Contact name Viviana Gallardo
E-mail(s) gallardov@mail.nih.gov
Phone 301-594-9221
Organization name NHGRI/NIH
Street address 50 South Dr. Bldg 50. Room 5535
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platforms (1)
GPL4021 Zebrafish 34K (Compugen, MWG, Operon)
Samples (16)
GSM629521 D.rerio_GFP+ cells vs GFP- cells from 36hpf embryos tails_1 Replicate 1
GSM629522 D.rerio_GFP+ cells vs GFP- cells from 36hpf embryos tails_1 Replicate 2
GSM629523 D.rerio_GFP+ cells vs GFP- cells from 36hpf embryos tails_1 Replicate 3
Relations
BioProject PRJNA133961

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE25617_RAW.tar 45.7 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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