Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors

Masayuki Akimoto(University of Michigan), Hong Cheng(Society for Neuroscience), Dongxiao Zhu(University of Michigan), Joseph A. Brzezinski(University of Michigan), Ritu Khanna(University of Michigan), Elena V. Filippova(University of Michigan), Edwin C. Oh(Society for Neuroscience), Yuezhou Jing(University of Michigan), Jose-Luis Linares(University of Michigan), Matthew Brooks(University of Michigan), Sepideh Zareparsi(University of Michigan), Alan J. Mears(University of Ottawa), Alfred O. Hero(University of Michigan), Tom Glaser(University of Michigan), Anand Swaroop(Kyoto University Hospital)
Proceedings of the National Academy of Sciences
February 27, 2006
Cited by 315Open Access
Full Text

Abstract

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.


Related Papers

No related papers found

Powered by citation graph analysis