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- Brock, Daniel C1
- Brockerhoff, Susan E1
- Burrell, Anika L1
- Chambers, Zachary S1
- Chan, Lawrence1
- Contreras, Laura1
- Djukovic, Danijel1
- Giarmarco, Michelle M1
- Gu, Haiwei1
- Hurley, James B1
- Kanow, Mark1
- Kollman, Justin M1
- Lindsay, Ken J1
- Raftery, Dan1
- Rountree, Austin1
- Sadilek, Martin1
- Satrústegui, Jorgina1
- Sweet, Ian R1
- Tsang, Stephen H1
- Wang, Yekai1
Keyword
- anaerobic metabolism1
- calcium1
- IHC1
- immunohistochemistry1
- IMPDH1
- inner segment1
- inosine monophosphate dehydrogenase1
- IS1
- metabolic filaments1
- mitochondria1
- photoreceptor1
- photoreceptor metabolism1
- photoreceptors1
- phototransduction1
- purine metabolism1
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Neurobiology
2 Results
- Research ArticleOpen Access
A highly conserved zebrafish IMPDH retinal isoform produces the majority of guanine and forms dynamic protein filaments in photoreceptor cells
Journal of Biological ChemistryVol. 298Issue 1101441Published online: November 19, 2021- Whitney M. Cleghorn
- Anika L. Burrell
- Michelle M. Giarmarco
- Daniel C. Brock
- Yekai Wang
- Zachary S. Chambers
- and others
Cited in Scopus: 2Inosine monophosphate dehydrogenase (IMPDH) is a key regulatory enzyme in the de novo synthesis of the purine base guanine. Dominant mutations in human IMPDH1 cause photoreceptor degeneration for reasons that are unknown. Here, we sought to provide some foundational information on Impdh1a in the zebrafish retina. We found that in zebrafish, gene subfunctionalization due to ancestral duplication resulted in a predominant retinal variant expressed exclusively in rod and cone photoreceptors. This variant is structurally and functionally similar to the human IMPDH1 retinal variant and shares a reduced sensitivity to GTP-mediated inhibition. - MetabolismOpen Access
Phototransduction Influences Metabolic Flux and Nucleotide Metabolism in Mouse Retina
Journal of Biological ChemistryVol. 291Issue 9p4698–4710Published online: December 16, 2015- Jianhai Du
- Austin Rountree
- Whitney M. Cleghorn
- Laura Contreras
- Ken J. Lindsay
- Martin Sadilek
- and others
Cited in Scopus: 64Production of energy in a cell must keep pace with demand. Photoreceptors use ATP to maintain ion gradients in darkness, whereas in light they use it to support phototransduction. Matching production with consumption can be accomplished by coupling production directly to consumption. Alternatively, production can be set by a signal that anticipates demand. In this report we investigate the hypothesis that signaling through phototransduction controls production of energy in mouse retinas. We found that respiration in mouse retinas is not coupled tightly to ATP consumption.