2002
DOI: 10.1128/mcb.22.21.7501-7511.2002
|View full text |Cite
|
Sign up to set email alerts
|

Circadian Regulation of nocturnin Transcription by Phosphorylated CREB in Xenopus Retinal Photoreceptor Cells

Abstract: Although CLOCK/BMAL1 heterodimers have been implicated in transcriptional regulation of several rhythmic genes in vitro through E-box sequence elements, little is known about how the circadian clock regulates rhythmic genes with diverse phases in vivo. The gene nocturnin is rhythmically transcribed in Xenopus retinal photoreceptor cells, which contain endogenous circadian clocks. Transcription of nocturnin peaks in these cells in the middle of the night, while CLOCK/BMAL1 activity peaks during the early mornin… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
18
0

Year Published

2004
2004
2018
2018

Publication Types

Select...
9
1

Relationship

1
9

Authors

Journals

citations
Cited by 24 publications
(19 citation statements)
references
References 75 publications
(92 reference statements)
1
18
0
Order By: Relevance
“…6). These results are consistent with studies showing circadian control of cAMP levels in chick photoreceptors and pinealocytes (Nikaido and Takahashi, 1998;Ivanova and Iuvone, 2003) and of phospho-cAMP response element-binding protein levels in Xenopus photoreceptors (Liu and Green, 2002), all of which are high at night.…”
Section: Discussionsupporting
confidence: 81%
“…6). These results are consistent with studies showing circadian control of cAMP levels in chick photoreceptors and pinealocytes (Nikaido and Takahashi, 1998;Ivanova and Iuvone, 2003) and of phospho-cAMP response element-binding protein levels in Xenopus photoreceptors (Liu and Green, 2002), all of which are high at night.…”
Section: Discussionsupporting
confidence: 81%
“…Digoxigenin-labeled antisense T7 and sense T3 probes (Roche, Indianapolis, IN) were prepared, and in situ hybridization was performed (Liu and Green, 2002). Peroxidase-conjugated anti-digoxigenin-peroxidase (1:500; Roche) was used to detect hybridized cRNA probes.…”
Section: Methodsmentioning
confidence: 99%
“…VGLUT2 full-length cDNA was used for in situ hybridization (Fremeau et al, 2001). Digoxigenin-labeled antisense T7 and sense T3 probes (Roche, Palo Alto, CA) were prepared and applied as described previously (Liu and Green, 2002). Peroxidase-conjugated antidigoxigenin peroxidase (1:500; Roche) was used to detect hybridized cRNA probes.…”
Section: Methodsmentioning
confidence: 99%