Evidence map›Paper›PMID 22773946›Full record

ArticleScientific reports2012

Intersectional Cre driver lines generated using split-intein mediated split-Cre reconstitution.

Ping Wang, Tianrui Chen, Katsuyasu Sakurai, Bao-Xia Han, Zhigang He, Guoping Feng, Fan Wang

Abstract read
In one paragraph

Article in Scientific reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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  10. Review
  11. Article
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  17. Article
  18. Article
  19. Biotechnological Applications of Protein Splicing.Current protein & peptide science · 2019
    Review
  20. Neural lineage tracing in the mammalian brain.Current opinion in neurobiology · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ping WangDepartment of Cell Biology, Box 3709, Duke University Medical Center, Durham, NC, USA.
Tianrui Chen
Katsuyasu Sakurai
Bao-Xia Han
Zhigang He
Guoping Feng
Fan Wang

Funding

Roles of SAPAP Proteins in Synaptic Function and Compulsive-like BehaviorR01MH081201 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FENG, GUOPING · 2007 to 2011
$1.8M
Genetically encoded anatomical probes for neuronal activity and plasticityR01DA028302 · NIDA · DUKE UNIVERSITY · PI WANG, FAN · 2009 to 2012
$1.2M
CNS Region Specific Cre/CreER Transgenic Mouse Lines Driven by Conserved Human EnRC1NS068612 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI HE, ZHIGANG · 2009 to 2010
$1000k
NIDA NIH HHS DA028302NIDA NIH HHS R01 DA028302NIMH NIH HHS R01 MH081201NINDS NIH HHS RC1 NS068612NINDS NIH HHS RC1NS068612
6 · The paper itself

Abstract

Tissue and cell type highly specific Cre drivers are very rare due to the fact that most genes or promoters used to direct Cre expressions are generally expressed in more than one tissues and/or in multiple cell types. We developed a split-intein based split-Cre system for highly efficient Cre-reconstitution through protein splicing. This split-intein-split-Cre system can be used to intersect the expression patterns of two genes or promoters to restrict full-length Cre reconstitution in their overlapping domains. To test this system in vivo, we selected several conserved human enhancers to drive the expression of either Cre-N-intein-N, or intein-C-Cre-C transgene in different brain regions. In all paired CreN/CreC transgenic mice, Cre-dependent reporter was efficiently induced specifically in the intersectional expression domains of two enhancers. This split-intein based method is simpler to implement compared with other strategies for generating highly-restricted intersectional Cre drivers to study complex tissues such as the nervous system.

Indexed as

AnimalsCell LineFemaleGene ExpressionGene Expression Regulation, DevelopmentalGene OrderGenetic VectorsHumansIntegrasesInteinsMiceMice, TransgenicProtein SplicingRecombinant Fusion ProteinsCre recombinaseIntegrasesRecombinant Fusion Proteins

Identifiers

PMID22773946
PMCPMC3390602

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.