Редактирование: NR2E3 (раздел)

==Publications==

{{medline-entry
|title=Nuclear receptor Rev-erb alpha (Nr1d1) functions in concert with Nr2e3 to regulate transcriptional networks in the retina.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/21408158
|abstract=The majority of diseases in the retina are caused by genetic mutations affecting the development and function of photoreceptor cells. The transcriptional networks directing these processes are regulated by genes such as nuclear hormone receptors. The nuclear hormone receptor gene Rev-erb alpha/Nr1d1 has been widely studied for its role in the circadian cycle and cell metabolism, however its role in the retina is unknown. In order to understand the role of Rev-erb alpha/Nr1d1 in the retina, we evaluated the effects of loss of Nr1d1 to the developing retina and its co-regulation with the photoreceptor-specific nuclear receptor gene Nr2e3 in the developing and mature retina. Knock-down of Nr1d1 expression in the developing retina results in pan-retinal spotting and reduced retinal function by electroretinogram. Our studies show that [[NR1D1]] protein is co-expressed with [[NR2E3]] in the outer neuroblastic layer of the developing mouse retina. In the adult retina, [[NR1D1]] is expressed in the ganglion cell layer and is co-expressed with [[NR2E3]] in the outer nuclear layer, within rods and cones. Several genes co-targeted by [[NR2E3]] and [[NR1D1]] were identified that include: Nr2c1, Recoverin, Rgr, Rarres2, Pde8a, and Nupr1. We examined the cyclic expression of Nr1d1 and Nr2e3 over a twenty-four hour period and observed that both nuclear receptors cycle in a similar manner. Taken together, these studies reveal a novel role for Nr1d1, in conjunction with its cofactor Nr2e3, in regulating transcriptional networks critical for photoreceptor development and function.
|mesh-terms=* Aging
* Animals
* Cell Count
* Enhancer Elements, Genetic
* Gene Regulatory Networks
* Injections
* Light
* Light Signal Transduction
* Mice
* Nuclear Receptor Subfamily 1, Group D, Member 1
* Organ Specificity
* Orphan Nuclear Receptors
* Protein Transport
* RNA, Small Interfering
* Retina
* Staining and Labeling
* Transcriptional Activation

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050883
}}