Toolkit/antisense oligodeoxynucleotide against Per1
antisense oligodeoxynucleotide against Per1
Also known as: antisense ODN against Per1
Taxonomy: Mechanism Branch / Architecture. Workflows sit above the mechanism and technique branches rather than replacing them.
Summary
The antisense oligodeoxynucleotide against Per1 is a nucleic acid perturbation reagent used in the rat suprachiasmatic nucleus to suppress Per1 function during circadian signaling experiments. In the cited study, this antisense ODN blocked glutamate-induced phase advances, implicating Per1 in light-responsive clock resetting.
Usefulness & Problems
Why this is useful
This reagent is useful for testing whether Per1 is required in the signaling pathway that links light-stimulated glutamatergic input to circadian phase shifting in the suprachiasmatic nucleus. The available evidence supports its use as a loss-of-function perturbation in rat SCN tissue.
Problem solved
It addresses the problem of causally probing Per1 function in glutamate-triggered circadian phase advance responses. Specifically, it enables experimental suppression of Per1 to test whether this gene is necessary for SCN clock resetting downstream of light-associated glutamatergic neurotransmission.
Problem links
Need conditional recombination or state switching
DerivedThe antisense oligodeoxynucleotide against Per1 is a nucleic acid perturbation reagent used in the rat suprachiasmatic nucleus to suppress Per1 function during circadian signaling experiments. In the cited study, this antisense ODN blocked glutamate-induced phase advances, implicating Per1 in light-responsive clock resetting.
Need precise spatiotemporal control with light input
DerivedThe antisense oligodeoxynucleotide against Per1 is a nucleic acid perturbation reagent used in the rat suprachiasmatic nucleus to suppress Per1 function during circadian signaling experiments. In the cited study, this antisense ODN blocked glutamate-induced phase advances, implicating Per1 in light-responsive clock resetting.
Taxonomy & Function
Primary hierarchy
Mechanism Branch
Architecture: A reusable architecture pattern for arranging parts into an engineered system.
Mechanisms
antisense-mediated gene suppressionTechniques
No technique tags yet.
Target processes
recombinationInput: Light
Implementation Constraints
The available evidence indicates use in the rat suprachiasmatic nucleus in the context of glutamate-induced phase-advance assays. No sequence, chemistry, dosing, delivery method, or expression-system details are provided in the supplied evidence.
The evidence is limited to a single cited study in rat suprachiasmatic nucleus and reports a phase-shift phenotype without detailed construct, sequence, or delivery information here. The supplied evidence does not document independent replication, quantitative knockdown efficiency, off-target assessment, or validation in other organisms or preparations.
Validation
Observations
Inferred from claim c2 during normalization. Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus. Derived from claim c2. Section: abstract. Quoted text: Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Inferred from claim c2 during normalization. Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus. Derived from claim c2. Section: abstract. Quoted text: Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Inferred from claim c2 during normalization. Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus. Derived from claim c2. Section: abstract. Quoted text: Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Inferred from claim c2 during normalization. Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus. Derived from claim c2. Section: abstract. Quoted text: Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Inferred from claim c2 during normalization. Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus. Derived from claim c2. Section: abstract. Quoted text: Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Inferred from claim c2 during normalization. Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus. Derived from claim c2. Section: abstract. Quoted text: Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Inferred from claim c2 during normalization. Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus. Derived from claim c2. Section: abstract. Quoted text: Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Supporting Sources
Ranked Claims
CRE-decoy oligodeoxynucleotide blocks glutamate-induced accumulation of Per1 mRNA.
Furthermore, the CRE-decoy blocked GLU-induced accumulation of Per1 mRNA.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced accumulation of Per1 mRNA.
Furthermore, the CRE-decoy blocked GLU-induced accumulation of Per1 mRNA.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced accumulation of Per1 mRNA.
Furthermore, the CRE-decoy blocked GLU-induced accumulation of Per1 mRNA.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced accumulation of Per1 mRNA.
Furthermore, the CRE-decoy blocked GLU-induced accumulation of Per1 mRNA.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced accumulation of Per1 mRNA.
Furthermore, the CRE-decoy blocked GLU-induced accumulation of Per1 mRNA.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced accumulation of Per1 mRNA.
Furthermore, the CRE-decoy blocked GLU-induced accumulation of Per1 mRNA.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced accumulation of Per1 mRNA.
Furthermore, the CRE-decoy blocked GLU-induced accumulation of Per1 mRNA.
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
CRE-decoy oligodeoxynucleotide blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1 and Ca(2+)/cAMP response element (CRE)-decoy ODN.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1 and Ca(2+)/cAMP response element (CRE)-decoy ODN.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1 and Ca(2+)/cAMP response element (CRE)-decoy ODN.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1 and Ca(2+)/cAMP response element (CRE)-decoy ODN.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1 and Ca(2+)/cAMP response element (CRE)-decoy ODN.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1 and Ca(2+)/cAMP response element (CRE)-decoy ODN.
CRE-decoy oligodeoxynucleotide blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1 and Ca(2+)/cAMP response element (CRE)-decoy ODN.
CRE-decoy oligodeoxynucleotide blocks light-induced phase advances in vivo.
CRE-decoy ODN also blocked light-induced phase advances in vivo.
CRE-decoy oligodeoxynucleotide blocks light-induced phase advances in vivo.
CRE-decoy ODN also blocked light-induced phase advances in vivo.
CRE-decoy oligodeoxynucleotide blocks light-induced phase advances in vivo.
CRE-decoy ODN also blocked light-induced phase advances in vivo.
CRE-decoy oligodeoxynucleotide blocks light-induced phase advances in vivo.
CRE-decoy ODN also blocked light-induced phase advances in vivo.
CRE-decoy oligodeoxynucleotide blocks light-induced phase advances in vivo.
CRE-decoy ODN also blocked light-induced phase advances in vivo.
CRE-decoy oligodeoxynucleotide blocks light-induced phase advances in vivo.
CRE-decoy ODN also blocked light-induced phase advances in vivo.
CRE-decoy oligodeoxynucleotide blocks light-induced phase advances in vivo.
CRE-decoy ODN also blocked light-induced phase advances in vivo.
CREB-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock.
Ca2+/cAMP Response Element-binding Protein (CREB)-dependent Activation of Per1 Is Required for Light-induced Signaling in the Suprachiasmatic Nucleus Circadian Clock
CREB-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock.
Ca2+/cAMP Response Element-binding Protein (CREB)-dependent Activation of Per1 Is Required for Light-induced Signaling in the Suprachiasmatic Nucleus Circadian Clock
CREB-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock.
Ca2+/cAMP Response Element-binding Protein (CREB)-dependent Activation of Per1 Is Required for Light-induced Signaling in the Suprachiasmatic Nucleus Circadian Clock
CREB-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock.
Ca2+/cAMP Response Element-binding Protein (CREB)-dependent Activation of Per1 Is Required for Light-induced Signaling in the Suprachiasmatic Nucleus Circadian Clock
CREB-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock.
Ca2+/cAMP Response Element-binding Protein (CREB)-dependent Activation of Per1 Is Required for Light-induced Signaling in the Suprachiasmatic Nucleus Circadian Clock
CREB-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock.
Ca2+/cAMP Response Element-binding Protein (CREB)-dependent Activation of Per1 Is Required for Light-induced Signaling in the Suprachiasmatic Nucleus Circadian Clock
CREB-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock.
Ca2+/cAMP Response Element-binding Protein (CREB)-dependent Activation of Per1 Is Required for Light-induced Signaling in the Suprachiasmatic Nucleus Circadian Clock
Approval Evidence
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
CREB and Per1 are integral components of the pathway that transduces light-stimulated glutamatergic neurotransmission into phase advance of the circadian clock.
Thus, Ca(2+)/cAMP response element-binding protein (CREB) and Per1 are integral components of the pathway transducing light-stimulated GLU neurotransmission into phase advance of the circadian clock.
Source:
Antisense oligodeoxynucleotide against Per1 blocks glutamate-induced phase advances in the rat suprachiasmatic nucleus.
Glutamate (GLU)-induced phase advances in the rat SCN were blocked by antisense oligodeoxynucleotide (ODN) against Per1
Source:
Comparisons
Source-backed strengths
The reported strength is a clear functional phenotype: antisense oligodeoxynucleotide against Per1 blocked glutamate-induced phase advances in the rat SCN. The same study also places Per1 within a CREB-dependent light-signaling pathway, providing pathway-level context for the perturbation result.
antisense oligodeoxynucleotide against Per1 and modular light-controlled skeletal muscle-powered bioactuator address a similar problem space because they share recombination.
Shared frame: same top-level item type; shared target processes: recombination; same primary input modality: light
Compared with Opto-Casp8-V2
antisense oligodeoxynucleotide against Per1 and Opto-Casp8-V2 address a similar problem space because they share recombination.
Shared frame: same top-level item type; shared target processes: recombination; same primary input modality: light
Compared with pcVP16
antisense oligodeoxynucleotide against Per1 and pcVP16 address a similar problem space because they share recombination.
Shared frame: same top-level item type; shared target processes: recombination; same primary input modality: light
Ranked Citations
- 1.