Toolkit/DAT-Cre

DAT-Cre

Construct Pattern·Research·Since 2012

Taxonomy: Mechanism Branch / Architecture. Workflows sit above the mechanism and technique branches rather than replacing them.

Summary

The supplied web research summary explicitly identifies DAT-Cre as a genetic targeting component used in selective dopamine-neuron stimulation and terminal-dynamics studies relevant to this review topic.

Usefulness & Problems

Why this is useful

DAT-Cre is a genetic targeting component used to direct optogenetic tools to dopamine-neuron populations. The supplied summary links it to studies of terminal dopamine dynamics and selective stimulation.; selective targeting of dopamine neurons for optogenetic studies; studies of terminal dopamine dynamics

Source:

DAT-Cre is a genetic targeting component used to direct optogenetic tools to dopamine-neuron populations. The supplied summary links it to studies of terminal dopamine dynamics and selective stimulation.

Source:

selective targeting of dopamine neurons for optogenetic studies

Source:

studies of terminal dopamine dynamics

Problem solved

It helps achieve dopamine-neuron-selective expression needed for causal optogenetic experiments.; enables targeted opsin expression in dopamine-neuron populations

Source:

It helps achieve dopamine-neuron-selective expression needed for causal optogenetic experiments.

Source:

enables targeted opsin expression in dopamine-neuron populations

Problem links

enables targeted opsin expression in dopamine-neuron populations

Literature

It helps achieve dopamine-neuron-selective expression needed for causal optogenetic experiments.

Source:

It helps achieve dopamine-neuron-selective expression needed for causal optogenetic experiments.

Taxonomy & Function

Primary hierarchy

Mechanism Branch

Architecture: A reusable architecture pattern for arranging parts into an engineered system.

Techniques

No technique tags yet.

Target processes

recombination

Input: Light

Implementation Constraints

cofactor dependency: cofactor requirement unknownencoding mode: genetically encodedimplementation constraint: context specific validationimplementation constraint: payload burdenimplementation constraint: spectral hardware requirementoperating role: regulator

It requires a Cre-dependent payload and the corresponding transgenic or recombinase-based targeting setup.; requires compatible Cre-dependent expression strategy

The provided evidence does not specify how it compares with TH-Cre in specificity or coverage.; the provided payload does not include review-level comparison against TH-Cre or other targeting strategies

Validation

Cell-freeBacteriaMammalianMouseHumanTherapeuticIndep. Replication

Supporting Sources

Ranked Claims

Claim 1methodology summarysupports2012Source 1needs review

In source material connected to this review, ChR2 and NpHR are explicit optogenetic actuators used to interrogate dopamine circuits, while FSCV is an explicit paired measurement method for dopamine release dynamics.

Explicitly supported related components/tools include ChR2, NpHR, fast-scan cyclic voltammetry (FSCV), TH-Cre, DAT-Cre, and recombinase-driver rat lines.
Claim 2targeting summarysupports2012Source 1needs review

Selective genetic targeting is a central enabling component in dopamine optogenetics, with TH-Cre, DAT-Cre, and recombinase-driver rat lines identified as relevant targeting tools in source material connected to this review.

Explicitly supported related components/tools include ChR2, NpHR, fast-scan cyclic voltammetry (FSCV), TH-Cre, DAT-Cre, and recombinase-driver rat lines.

Approval Evidence

1 source1 linked approval claimfirst-pass slug dat-cre
The supplied web research summary explicitly identifies DAT-Cre as a genetic targeting component used in selective dopamine-neuron stimulation and terminal-dynamics studies relevant to this review topic.

Source:

targeting summarysupports

Selective genetic targeting is a central enabling component in dopamine optogenetics, with TH-Cre, DAT-Cre, and recombinase-driver rat lines identified as relevant targeting tools in source material connected to this review.

Explicitly supported related components/tools include ChR2, NpHR, fast-scan cyclic voltammetry (FSCV), TH-Cre, DAT-Cre, and recombinase-driver rat lines.

Source:

Comparisons

Source-stated alternatives

The summary mentions TH-Cre and recombinase-driver rat lines as related targeting approaches.

Source:

The summary mentions TH-Cre and recombinase-driver rat lines as related targeting approaches.

Source-backed strengths

used in studies of selective dopamine-neuron stimulation and terminal dynamics

Source:

used in studies of selective dopamine-neuron stimulation and terminal dynamics

The summary mentions TH-Cre and recombinase-driver rat lines as related targeting approaches.

Shared frame: source-stated alternative in extracted literature

Strengths here: used in studies of selective dopamine-neuron stimulation and terminal dynamics.

Relative tradeoffs: the provided payload does not include review-level comparison against TH-Cre or other targeting strategies.

Source:

The summary mentions TH-Cre and recombinase-driver rat lines as related targeting approaches.

Compared with TH-Cre

The summary mentions TH-Cre and recombinase-driver rat lines as related targeting approaches.

Shared frame: source-stated alternative in extracted literature

Strengths here: used in studies of selective dopamine-neuron stimulation and terminal dynamics.

Relative tradeoffs: the provided payload does not include review-level comparison against TH-Cre or other targeting strategies.

Source:

The summary mentions TH-Cre and recombinase-driver rat lines as related targeting approaches.

Ranked Citations

  1. 1.
    StructuralSource 1Brain Research2012Claim 1Claim 2

    Extracted from this source document.