Evidence map›Paper›PMID 39131308›Full record

ArticlebioRxiv : the preprint server for biology2024

CRISPR-Cas13d as a molecular tool to achieve targeted gene expression knockdown in chick embryos.

Minyoung Kim, Erica J Hutchins

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Minyoung KimDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-9502-1626
Erica J HutchinsDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-4316-0333

Funding

UCSF INTEGRATED DDS-PHD TRAINING PROGRAMT32DE007306 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Yukiko Nakano · 1996 to 2026
$15.4M
Mechanisms of RNA turnover during the epithelial-mesenchymal transitionR35GM150763 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Erica Hutchins · 2023 to 2026
$1.6M
Characterization of the roles and regulation of Draxin in cranial neural crestR00DE028592 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUTCHINS, ERICA · 2022 to 2024
$1.1M
NIDCR NIH HHS R00 DE028592NIDCR NIH HHS T32 DE007306NIGMS NIH HHS R35 GM150763
6 · The paper itself

Abstract

The chick embryo is a classical model system commonly used in developmental biology due to its amenability to gene perturbation experiments. Pairing this powerful model organism with cutting-edge technology can significantly expand the range of experiments that can be performed. Recently, the CRISPR-Cas13d system has been successfully adapted for use in zebrafish, medaka, killifish, and mouse embryos to achieve targeted gene expression knockdown. Despite its success in other animal models, no prior study has explored the potential of CRISPR-Cas13d in the chick. Here, we present an adaptation of the CRISPR-Cas13d system to achieve targeted gene expression knockdown in the chick embryo. As proof-of-principle, we demonstrate the knockdown of PAX7, an early neural crest marker. Application of this adapted CRISPR-Cas13d technique resulted in effective knockdown of PAX7 expression and function, comparable to knockdown achieved by translation-blocking morpholino. CRISPR-Cas13d complements preexisting knockdown tools such as CRISPR-Cas9 and morpholinos, thereby expanding the experimental potential and versatility of the chick model system.

Indexed as

Cas13dChickCRISPRNeural crest

Identifiers

PMID39131308
PMCPMC11312552

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.