Evidence map›Paper›PMID 37909037›Full record

ArticleNeuron2024

Viral vector-mediated transgene delivery with novel recombinase systems for targeting neuronal populations defined by multiple features.

Minju Jeong, Jun-Hyeok Choi, Hyeonseok Jang, Dong Hyun Sohn, Qingdi Wang, Joann Lee, Li Yao, Eun Ji Lee, Jiachen Fan, Marta Pratelli and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Neuron, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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

18 authors at 5 institutions in 2 countries.

Minju JeongNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Jun-Hyeok ChoiNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Hyeonseok JangNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Dong Hyun SohnDepartment of Microbiology and Immunology, Pusan National University School of Medicine, Yangsan 50612, Republic of Korea.
Qingdi WangNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Joann LeeNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Li YaoNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Eun Ji LeeNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Jiachen FanNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Marta PratelliNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Eric H WangNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Christen N SnyderDepartment of Biological Sciences and Center for the Neural Basis of Cognition, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Xiao-Yun WangNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Sora ShinCenter for Neurobiology Research, Fralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA; Department of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA.
Aryn H GittisDepartment of Biological Sciences and Center for the Neural Basis of Cognition, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Tsung-Chang SungTransgenic Core, Salk Institute for Biological Studies, La Jolla, CA, USA.
Nicholas C SpitzerNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Byung Kook LimNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA. Electronic address: bklim@ucsd.edu.
University of California San Diego · USCenter for the Neural Basis of Cognition · USPusan National University · KRSalk Institute for Biological Studies · USVirginia Tech · US

Funding

Anatomical characterization of neuronal cell types of the mouse brainU01MH114829 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ASCOLI, GIORGIO A, DONG, HONG-WEI · 2017 to 2021
$13.9M
NEUROBIOLOGY TRAINING PROGRAMT32NS007220 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JIN, YISHI · 1985 to 2023
$4.5M
Role of Glutamatergic Neurons in External Globus Pallidus in the Behavioral Deficits in Animal Models of Progressive Dopamine DepletionR01NS121231 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LEUTGEB, STEFAN, LIM, BYUNGKOOK · 2021 to 2025
$2.5M
Dissecting the role of ventral pallidal circuitry in cocaine seeking after the withdrawalR01DA049787 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LIM, BYUNGKOOK · 2020 to 2024
$1.8M
NIDA NIH HHS R01 DA049787NIMH NIH HHS U01 MH114829NINDS NIH HHS R01 NS121231NINDS NIH HHS T32 NS007220
6 · The paper itself

Abstract

A comprehensive understanding of neuronal diversity and connectivity is essential for understanding the anatomical and cellular mechanisms that underlie functional contributions. With the advent of single-cell analysis, growing information regarding molecular profiles leads to the identification of more heterogeneous cell types. Therefore, the need for additional orthogonal recombinase systems is increasingly apparent, as heterogeneous tissues can be further partitioned into increasing numbers of specific cell types defined by multiple features. Critically, new recombinase systems should work together with pre-existing systems without cross-reactivity in vivo. Here, we introduce novel site-specific recombinase systems based on ΦC31 bacteriophage recombinase for labeling multiple cell types simultaneously and a novel viral strategy for versatile and robust intersectional expression of any transgene. Together, our system will help researchers specifically target different cell types with multiple features in the same animal.

Indexed as

IntegrasesRecombinasesAnimalsGenetic VectorsNeuronsTransgenesIntegrasesRecombinasesgene deliveryintersectional strategynew recombinaseviral tools

Identifiers

PMID37909037
PMCPMC10916502
OpenAlexW4388024587

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.