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Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines.

Authors :
Elrick H
Peterson KA
Willis BJ
Lanza DG
Acar EF
Ryder EJ
Teboul L
Kasparek P
Birling MC
Adams DJ
Bradley A
Braun RE
Brown SD
Caulder A
Codner GF
DeMayo FJ
Dickinson ME
Doe B
Duddy G
Gertsenstein M
Goodwin LO
Hérault Y
Lintott LG
Lloyd KCK
Lorenzo I
Mackenzie M
Mallon AM
McKerlie C
Parkinson H
Ramirez-Solis R
Seavitt JR
Sedlacek R
Skarnes WC
Smedley D
Wells S
White JK
Wood JA
Murray SA
Heaney JD
Nutter LMJ
Source :
Scientific reports [Sci Rep] 2024 Sep 30; Vol. 14 (1), pp. 22626. Date of Electronic Publication: 2024 Sep 30.
Publication Year :
2024

Abstract

The International Mouse Phenotyping Consortium (IMPC) systematically produces and phenotypes mouse lines with presumptive null mutations to provide insight into gene function. The IMPC now uses the programmable RNA-guided nuclease Cas9 for its increased capacity and flexibility to efficiently generate null alleles in the C57BL/6N strain. In addition to being a valuable novel and accessible research resource, the production of 3313 knockout mouse lines using comparable protocols provides a rich dataset to analyze experimental and biological variables affecting in vivo gene engineering with Cas9. Mouse line production has two critical steps - generation of founders with the desired allele and germline transmission (GLT) of that allele from founders to offspring. A systematic evaluation of the variables impacting success rates identified gene essentiality as the primary factor influencing successful production of null alleles. Collectively, our findings provide best practice recommendations for using Cas9 to generate alleles in mouse essential genes, many of which are orthologs of genes linked to human disease.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
2045-2322
Volume :
14
Issue :
1
Database :
MEDLINE
Journal :
Scientific reports
Publication Type :
Academic Journal
Accession number :
39349521
Full Text :
https://doi.org/10.1038/s41598-024-72418-8