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Series GSE35396 Query DataSets for GSE35396
Status Public on Jul 26, 2012
Title Selective knockout of NeuroD1 in the retina and pineal gland
Organism Mus musculus
Experiment type Expression profiling by array
Summary NeuroD1 encodes a basic helix-loop-helix transcription factor involved in the development of neural and endocrine structures. NeuroD1 mRNA is highly abundant in the adult mammalian pineal gland and exhibits a developmental expression pattern similar to the retina. This is consistent with the common evolutionary origin of pinealocytes and retinal photoreceptors. Pinealocytes and retinal photoreceptors express a shared set of phototransduction genes and submammalian pinealocytes are photosensitive. In contrast to the retina, the pineal gland is a relatively homogeneous structure, composed 95% of pinealocytes. This makes the pineal gland a particularly useful model for understanding photoreceptor cell biology. The loss of NeuroD1 in the retina results in progressive photoreceptor degeneration and the molecular mechanisms underlying this retinal degeneration phenotype remain unknown. Similarly, the role that NeuroD1 plays in the pineal gland is unknown.

To determine the function of NeuroD1 in the pineal gland and retina, a Cre/loxP recombination strategy was used to selectively target a NeuroD1 floxed allele and generate NeuroD1 conditional knockout (cKO) mice. Tissue specificity was conferred using Cre recombinase expressed under the control of the promoter of Crx, a transcription factor selectively expressed in the pineal gland and retina. Pineal and retinal tissues from two-month-old NeuroD1 cKO and control animals were used in microarray studies to identify candidate genes responsible for the photoreceptor degeneration phenotype.
 
Overall design The Cre/loxP recombination strategy was used to target a NeuroD1 floxed allele and generate NeuroD1 conditional knockout mice (NeuroD1floxed::Crx-Cre+/-). NeuroD1 floxed mice (NeuroD1floxed::Crx-Cre-/-) served as the controls. Pineal glands and retinas from two-month-old control and conditional knockout mice were collected at ZT6 and ZT20. 3 pools of 6 pineal glands per genotype and respective time of day were collected for each sample. Similarly, 3 pools of 6 retinas each were also collected. RNA from each pool was extracted and hybridized on the Affymetrix Mouse 430 2.0 array.
 
Contributor(s) Ochocinska MJ, Munoz EM, Veleri S, Weller JL, Coon SL, Pozdeyev NV, Goebbels S, Iuvone PM, Furukawa T, Nave KA, Klein DC
Citation(s) 22784109
Submission date Jan 28, 2012
Last update date Feb 11, 2019
Contact name Margaret Ochocinska
E-mail(s) ochocinm@mail.nih.gov
Phone 301-451-6627
Fax 301-480-3526
Organization name National Institutes of Health
Department NICHD/PDEGEN
Lab Section on Neuroendocrinology
Street address 49 Convent Dr. Rm.6A71
City Bethesda
ZIP/Postal code 20892
Country USA
 
Platforms (1)
GPL1261 [Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array
Samples (24)
GSM867301 Pineal gland from control mouse at ZT6, biological rep 1
GSM867302 Pineal gland from control mouse at ZT6, biological rep 2
GSM867303 Pineal gland from control mouse at ZT6, biological rep 3
Relations
BioProject PRJNA152703

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
GSE35396_RAW.tar 99.2 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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