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Links from GEO DataSets

Items: 20

1.

Systematic analysis of differential rhythmic gene expression mediated by the circadian clock and feeding rhythms in mouse liver

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17021 GPL19057
120 Samples
Download data
Series
Accession:
GSE149698
ID:
200149698
2.

Temporal profiles of gene expression in Cry1/2 KO, Bmal1 KO under night restricted feeding and ad libitum feeding regimen

(Submitter supplied) The circadian clock and rhythmic food intake are both important regulators of rhythmic gene expression in the liver. It remains, however, elusive to which extent the circadian clock network and natural feeding rhythms contribute to rhythmic gene expression. To systematically address this question, we developed an algorithm to investigate differential rhythmicity between a varying number of conditions. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
96 Samples
Download data: TXT
Series
Accession:
GSE135898
ID:
200135898
3.

Temporal profiles of hepatic gene expression in PAR bZip triple knockout mice

(Submitter supplied) The circadian clock and rhythmic food intake are both important regulators of rhythmic gene expression in the liver. It remains, however, elusive to which extent the circadian clock network and natural feeding rhythms contribute to rhythmic gene expression. To systematically address this question, we developed an algorithm to investigate differential rhythmicity between a varying number of conditions. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
24 Samples
Download data: TXT
Series
Accession:
GSE135875
ID:
200135875
4.

Regulatory logic of the coupled diurnal and feeding cycles in the mouse liver

(Submitter supplied) This study is a follow-up to GSE35790. This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL9185 GPL17021 GPL6246
59 Samples
Download data: BW, CEL, TXT
Series
Accession:
GSE60578
ID:
200060578
5.

Circadian and feeding rhythms differentially affect rhythmic mRNA transcription and translation in mouse liver

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL17021
168 Samples
Download data: TXT
Series
Accession:
GSE73554
ID:
200073554
6.

Circadian and feeding rhythms differentially affect rhythmic mRNA transcription and translation in mouse liver [Ribosome Profiling]

(Submitter supplied) Diurnal oscillations of gene expression are a hallmark of rhythmic physiology across most living organisms. Such oscillations are controlled by the interplay between the circadian clock and feeding rhythms. While rhythmic mRNA accumulation has been extensively studied, comparatively less is known about their transcription and translation. Here, we quantified simultaneously temporal transcription, accumulation, and translation of mouse liver mRNAs under physiological light-dark conditions and ad libitum or night-restricted feeding in wild-type and Bmal1 deficient animals. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL17021
84 Samples
Download data
Series
Accession:
GSE73553
ID:
200073553
7.

Circadian and feeding rhythms differentially affect rhythmic mRNA transcription and translation in mouse liver [RNASeq]

(Submitter supplied) Diurnal oscillations of gene expression are a hallmark of rhythmic physiology across most living organisms. Such oscillations are controlled by the interplay between the circadian clock and feeding rhythms. While rhythmic mRNA accumulation has been extensively studied, comparatively less is known about their transcription and translation. Here, we quantified simultaneously temporal transcription, accumulation, and translation of mouse liver mRNAs under physiological light-dark conditions and ad libitum or night-restricted feeding in wild-type and Bmal1 deficient animals. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
84 Samples
Download data
Series
Accession:
GSE73552
ID:
200073552
8.

Rhythmic Food Intake Drives Rhythmic Gene Expression More Potently than the Hepatic Circadian Clock in Mice

(Submitter supplied) Virtually every mammalian tissue exhibits rhythmic expression in thousands of genes, which activate tissue-specific processes at appropriate times of the day. Much of this rhythmic expression is thought to be driven cell-autonomously by molecular circadian clocks present throughout the body. However, increasing evidence suggests that systemic signals, and more specifically rhythmic food intake (RFI), can regulate rhythmic gene expression independently of the circadian clock. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
72 Samples
Download data: TXT
Series
Accession:
GSE118967
ID:
200118967
9.

Oscillating and stable promoter-enhancer loops underlie core- and clock-controlled gene expression rhythms in mouse liver

(Submitter supplied) The circadian clock dynamically rewires promoter-enhancer loops in tissues to drive robust daily rhythms in gene transcription and locomoter activity.
Organism:
Mus musculus
Type:
Other
Platform:
GPL17021
365 Samples
Download data: TXT
Series
Accession:
GSE139195
ID:
200139195
10.

Circadian clock controls rhythms in ketogenesis by interfering with PPARa transcriptional network

(Submitter supplied) Ketone bodies, intermediates in energy metabolism and signaling, have attracted significant attention due to their role in health and disease. We performed around the clock study on ketone bodies and ketogenesis with mice on different diets. We found that caloric restriction, a dietary intervention that improves metabolism and longevity, induced high amplitude circadian rhythms in blood βOHB. The blood βOHB rhythms resulted from rhythmic ketogenesis in the liver controlled by the interaction between the circadian clock and PPAR transcriptional networks. more...
Organism:
Mus musculus
Type:
Genome variation profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL24247
36 Samples
Download data: TXT
Series
Accession:
GSE211975
ID:
200211975
11.

Rewiring of liver diurnal transcriptome rhythms by triiodothyronine (T3) supplementation

(Submitter supplied) Diurnal (i.e., 24-hour) physiological rhythms depend on transcriptional programs controlled by a set of circadian clock genes/proteins. Systemic factors like humoral and neuronal signals, oscillations in body temperature, and food intake align physiological circadian rhythms with external time. Thyroid hormones (THs) are major regulators of circadian clock target processes such as energy metabolism, but little is known about how fluctuations in TH levels affect the circadian coordination of tissue physiology. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL23038
70 Samples
Download data: CEL
Series
Accession:
GSE199998
ID:
200199998
12.

Diurnal regulation of RNA polymerase III transcription is under the control of both feeding-fasting response and circadian clock

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL16570 GPL17021
186 Samples
Download data: BEDGRAPH, CEL
Series
Accession:
GSE89837
ID:
200089837
13.

Diurnal regulation of RNA polymerase III transcription is under the control of both feeding-fasting response and circadian clock [ChIP-Seq]

(Submitter supplied) RNA polymerase III (pol III) synthesizes short non-coding RNAs, many of which, including tRNAs, Rpph1 RNA, Rn5s rRNA, and Rmrp RNA, are essential for translation. Accordingly, pol III activity is tightly regulated with cell growth and proliferation by factors such as MYC, RB1, TRP53, and MAF1. MAF1 is a repressor of pol III transcription whose activity is controlled by phosphorylation; in particular, it is inactivated through phosphorylation by mTORC1 kinase, a sensor of nutrient availability. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
100 Samples
Download data: BEDGRAPH
Series
Accession:
GSE89833
ID:
200089833
14.

Diurnal regulation of RNA polymerase III transcription is under the control of both feeding-fasting response and circadian clock [Affymetrix]

(Submitter supplied) RNA polymerase III (pol III) synthesizes short non-coding RNAs, many of which, including tRNAs, Rpph1 RNA, Rn5s rRNA, and Rmrp RNA, are essential for translation. Accordingly, pol III activity is tightly regulated with cell growth and proliferation by factors such as MYC, RB1, TRP53, and MAF1. MAF1 is a repressor of pol III transcription whose activity is controlled by phosphorylation; in particular, it is inactivated through phosphorylation by mTORC1 kinase, a sensor of nutrient availability. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
86 Samples
Download data: CEL
Series
Accession:
GSE89658
ID:
200089658
15.

Achilles-mediated and sex-specific regulation of circadian mRNA rhythms in Drosophila

(Submitter supplied) The circadian clock is an evolutionarily conserved mechanism that drives rhythmic expression of downstream genes. The core circadian clock drives the expression of clock-controlled genes either directly or indirectly, which in turn play critical roles in carrying out many rhythmic physiological processes. Nevertheless, the molecular mechanisms by which clock output genes orchestrate rhythmic signals from the brain to peripheral tissues are largely unknown. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21306
96 Samples
Download data: TXT
Series
Accession:
GSE120100
ID:
200120100
16.

Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and delta-RRE Liver Transcriptomes

(Submitter supplied) In mammals, the circadian clock consists of transcriptional and translational feedback loops through DNA cis-elements such as E-box and RRE. In this study, we established mutant mice deficient for rhythmic transcription of Bmal1 gene by deleting its upstream RRE elements. We observed apparently normal circadian rhythms in the mutant, but the circadian period and amplitude of the mutants were more susceptible to disturbance of CRY1 protein rhythm. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
24 Samples
Download data: TXT
Series
Accession:
GSE199061
ID:
200199061
17.

Ribosome profiling reveals the rhythmic liver translatome and circadian clock regulation by upstream open reading frames

(Submitter supplied) Mammalian gene expression displays widespread circadian oscillations. Rhythmic transcription underlies the core clock mechanism, but it cannot explain numerous observations made at the level of protein rhythmicity. We have used ribosome profiling in mouse liver to measure the translation of mRNAs into protein around-the-clock and at high temporal and nucleotide resolution. Transcriptome-wide, we discovered extensive rhythms in ribosome occupancy, and identified a core set of ≈150 mRNAs subject to particularly robust daily changes in translation efficiency. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
48 Samples
Download data: TXT
Series
Accession:
GSE67305
ID:
200067305
18.

The diurnal rhythm of adipose tissue gene expression is reduced in obese patients with type 2 diabetes

(Submitter supplied) Animal studies have linked disturbed adipose tissue clock gene rhythms to the pathophysiology of the metabolic syndrome. However, data on molecular clock rhythms in human patients are limited. Therefore, in a standardized real life setting, we compared diurnal gene expression profiles in subcutaneous adipose tissue between obese patients with type 2 diabetes and age-matched healthy lean control subjects, using RNA sequencing. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16558
48 Samples
Download data: TXT, XLSX
Series
Accession:
GSE104674
ID:
200104674
19.

Non-circadian expression masking clock-driven weak transcription rhythms in U2OS cells

(Submitter supplied) U2OS cells harbor a circadian clock but express only a few rhythmic genes in constant conditions. We identified 3040 binding sites of the circadian regulators BMAL1, CLOCK and CRY1 in the U2OS genome. Most binding sites even in promoters do not correlate with detectable rhythmic transcript levels. Luciferase fusions reveal that the circadian clock supports robust but low amplitude transcription rhythms of representative promoters. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18721
32 Samples
Download data: DAT
Series
Accession:
GSE57891
ID:
200057891
20.

ChIP-seq of three core components of the circadian clock (BMAL1, CLOCK and CRY1) in unsynchronized human U2OS cells

(Submitter supplied) The human osteosarcoma cell line U2OS contains a functional circadian clock but expresses only a few rhythmic genes. We identified by ChIP-seq analysis 3040 binding sites of the circadian transcription factors BMAL1, CLOCK, and CRY1 in the genome of U2OS cells, comparable to the number found in highly rhythmic tissues like liver.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL10999
3 Samples
Download data: BEDGRAPH
Series
Accession:
GSE44236
ID:
200044236
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