published-canonicalconceptmaha-epistemic/1.0

CRISPR-Cas9 nuclease editing

RNA-guided DNA cleavage using a Cas9 nuclease and target-complementary guide sequence. This candidate preserves the experimental unit—editor or circuit, target, cell system, delivery, protocol, assay, comparator, and observation window—before any broader inference is considered.

Bounded definition

RNA-guided DNA cleavage using a Cas9 nuclease and target-complementary guide sequence.

What the cited work establishes

The study reconstitutes RNA-programmed Cas9 cleavage in vitro and shows that a designed single-guide RNA can direct sequence-specific DNA cleavage adjacent to an appropriate motif.

The constructs, biological systems, protocols, assays, datasets, and comparisons reported in A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.

Claims: urn:maha:claim:crispr-cas9-nuclease-editing

What remains a separate question

Biochemical cleavage is not equivalent to efficient, specific, or safe genome editing in a cell or organism.

An in-vitro nuclease mechanism does not establish editing efficiency, specificity, delivery, safety, or phenotype in cells or organisms.

Connected domain graph

Typed dependencies preserve publication state.

Only independently canonical records receive public links and relation statements. Draft graph topology remains private.

mechanistic dependencycanonical

Guide RNA and PAM recognition

outbound connection · mechanism

Target recognition depends on guide complementarity and a compatible adjacent motif.

mechanistic dependencycanonical

Guide RNA and PAM recognition

inbound connection · mechanism

Guide and motif recognition direct the nuclease mechanism.

mechanistic dependencycanonical

Double-strand-break repair outcomes

inbound connection · mechanism

Nuclease editing delegates the final sequence outcome to cellular break repair.

Claim ledger

Every proposition keeps its own evidence state.

empirical-claimsingle-study

The cited biochemical study reconstitutes programmable Cas9 cleavage and shows that a designed single guide can direct sequence-specific cutting adjacent to a compatible motif.

Scope
The constructs, biological systems, protocols, assays, datasets, and comparisons reported in A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.
Boundary
Biochemical cleavage is not equivalent to efficient, specific, or safe genome editing in a cell or organism.
Uncertainty
There is no universal effect estimate for this method; numerical results remain attached to the source experiment, biological system, assay, and analysis choices.
Replication
This candidate records one bounded source package. Independent replications and contradictory results must be compiled separately before evidence maturity is upgraded.

Primary sources

Citation, locator, rights, and boundary travel together.

  1. Source 1 · Science

    A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity

    Martin Jinek, Krzysztof Chylinski, Ines Fonfara, Michael Hauer, Jennifer A. Doudna, Emmanuelle Charpentier

    Exact locator
    Abstract; Figures 1–5; supplementary materials describing guide design and cleavage assays.
    Establishes
    The study reconstitutes RNA-programmed Cas9 cleavage in vitro and shows that a designed single-guide RNA can direct sequence-specific DNA cleavage adjacent to an appropriate motif.
    Boundary
    An in-vitro nuclease mechanism does not establish editing efficiency, specificity, delivery, safety, or phenotype in cells or organisms.
    Rights basis
    citation with paraphrase · Maha paraphrases the source-level result and links to the version of record; no article passage is reproduced.