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Expression Database
GUDMAP:21892
Gene:
Foxl2
, forkhead box L2
Stage:
Theiler Stage 23
Tissue:
urinary system
Species:
Mus musculus
Assay Type:
TG mouse marker strain
Images
Cre-dependent ?-gal activity in Foxl2GCE/+; R26RlacZ/+ UGS samples. A single dose of Tamoxifen (1mg/40g) results in a small number of X-gal positive cells in granulosa cell precursors located in the ovarian medulla of Foxl2GCE/+; R26RlacZ/+ embryos at 15.5dpc.
Cre-dependent ?-gal activity in Foxl2GCE/+; R26RlacZ/+ UGS samples. A single dose of Tamoxifen (1mg/40g) results in a small number of X-gal positive cells in the medulla of the ovaries of Foxl2GCE/+; R26RlacZ/+ embryos at 15.5dpc.
GFP is detected in cells adjacent to E-Cadherin positive germ cells in the medulla of the ovary in Foxl2GCE/+; R26RlacZ/+ embryos at 14.5dpc. Antibodies: chicken-anti-GFP/ rat-anti-E-Cadherin / rabbit-anti-Laminin.
GFP is detected in granulosa precursor cells distinct from E-Cadherin positive germ cells, in the ovary of Foxl2GCE/+; R26RlacZ/+ embryos at 14.5dpc. Antibodies: chicken-anti-GFP/ rat-anti-E-Cadherin.
Co-localization of ?-gal positive cells and GFP positive cells following Tamoxifen induction of Foxl2 driven GCE. Co-localization is observed in putative granulosa precursor cells in the center of the medulla in Foxl2GCE/+; R26RlacZ/+ ovaries at 14.5dpc. Antibodies: chicken-anti-GFP / rabbit-anti-?-gal / rat-anti-E-Cadherin.
Results Notes
Submitter findings: Analysis confirms the expression of Foxl2 driven eGFPCreERT2 in a small population of cells located in the medulla of the ovary at 14.5-15.5 dpc. The labeled cells are likely granulosa cell precursors. Native GFP expression was not detectable in our samples but could be visualized by immunohistochemistry. Cre dependent R26RLacZ expression was observed in a subset of GFP positive cells following Tamoxifen treatment.
Mouse marker strain entries are unique GUDMAP entries that can contain data for multiple probes at multiple stages of development (
more info
).
Submitters
Principal Investigator(s):
Andrew P McMahon,
Keck School of Medicine, Los Angeles, CA, USA, amcmahon@med.usc.edu
Contributors:
Andrew P McMahon, M Todd Valerius, Jinjin Guo, Jill McMahon
Submitted By:
Jill McMahon,
Keck School of Medicine, Los Angeles, CA, USA
Batch ID:
555
Submission ID:
21892
Expression Mapping
Expression Strengths Key:
Present (unspecified strength)
Present (strong)
Present (moderate)
Present (weak)
Uncertain
Not Detected
Expression Patterns Key:
Homogeneous
Graded
Regional
Spotted
Ubiquitous
Restricted
Single cell
Nerve Density:
Relative to Total:
High
Medium
Low
Relative to P0/Adult:
Increase, large
Increase, small
Decrease, large
Decrease, small
Contains note
View annotated components as a list
Show annotation under groups
Specimen
Stage:
TS23
Other Staging System:
15.5 dpc
Tissue:
urinary system
Strain:
mixed background
Genotype:
Non-wild type Allele:
Gene
Foxl2
MGI ID
MGI:4940388
MGI Symbol or lab name
Foxl2
tm1(GFP/cre/ERT2)Pzg
Type
Targeted, (Reporter|Inducible|Recombinase)
Allele First Chromatid
Foxl2
tm1(GFP/cre/ERT2)Pzg
Allele Second Chromatid
wild type
Notes:
Mouse strain is available from the Jackson Lab, see here: http://jaxmice.jax.org/strain/015854.html
Sex:
both
Specimen Preparation:
mouse marker strain
Fixation Method:
unspecified
Experiment Notes:
Transgene Visualisation
Reporter:
GFP
Direct method for visualising reporter:
Fluorescence
Acknowledgements
Comprehensive PDFs containing allele verification (provided by Zhang lab) and allele characterisation (provided by McMahon lab) can be downloaded from the GUDMAP mouse strains page (http://www.gudmap.org/Resources/MouseStrains/Mouse_Strains_Summary.html). GUDMAP:21892 entry compiled from PDFs by GUDMAP Editorial Office.