Proceedings of the National Academy of Sciences of the United States of America · 2006
Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Akimoto Masayuki, Cheng Hong, Zhu Dongxiao, Brzezinski Joseph A, Khanna Ritu, Filippova Elena, Oh Edwin C T, Jing Yuezhou, Linares Jose-Luis, Brooks Matthew, Zareparsi Sepideh, Mears Alan J, Hero Alfred, Glaser Tom, Swaroop Anand
Аннотация
The Maf-family transcription factor Nrl is a key regulator of photoreceptor differentiation in mammals. Ablation of the Nrl gene in mice leads to functional cones at the expense of rods. We show that a 2.5-kb Nrl promoter segment directs the expression of enhanced GFP specifically to rod photoreceptors and the pineal gland of transgenic mice. GFP is detected shortly after terminal cell division, corresponding to the timing of rod genesis revealed by birthdating studies. In Nrl-/- retinas, the GFP+ photoreceptors express S-opsin, consistent with the transformation of rod precursors into cones. We report the gene profiles of freshly isolated flow-sorted GFP+ photoreceptors from wild-type and Nrl-/- retinas at five distinct developmental stages. Our results provide a framework for establishing gene regulatory networks that lead to mature functional photoreceptors from postmitotic precursors. Differentially expressed rod and cone genes are excellent candidates for retinopathies.
Предметные рубрики MeSH
AnimalsAnimals, NewbornBasic-Leucine Zipper Transcription FactorsCell DifferentiationDNA-Binding ProteinsEye ProteinsGene Expression ProfilingGreen Fluorescent ProteinsHumansMiceMice, KnockoutMice, TransgenicNeuronsPhotoreceptor Cells, VertebratePromoter Regions, GeneticRecombinant ProteinsRetinaRetinal Cone Photoreceptor CellsRetinal Rod Photoreceptor Cells