Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors
Male
Mice, Transgenic
Transgenic
conditional gene targeting
Mice
03 medical and health sciences
Genetic
Cre-lox
Genes, Reporter
Genetics
Psychology
Animals
conditional knockout
Reporter
site-specific recombinase
mosaic recombination
parental sex bias
conditional knockin
Neurons
Recombination, Genetic
0303 health sciences
Neurology & Neurosurgery
Integrases
Mosaicism
Neurosciences
Spermatozoa
Recombination
3. Good health
conditional reporter
Germ Cells
Genes
molecular genetics
Gene Targeting
Oocytes
Cognitive Sciences
Female
germline recombination
Biotechnology
DOI:
10.1016/j.neuron.2020.01.008
Publication Date:
2020-02-05T15:32:53Z
AUTHORS (56)
ABSTRACT
The Cre-loxP system is invaluable for spatial and temporal control of gene knockout, knockin, and reporter expression in the mouse nervous system. However, we report varying probabilities of unexpected germline recombination in distinct Cre driver lines designed for nervous system-specific recombination. Selective maternal or paternal germline recombination is showcased with sample Cre lines. Collated data reveal germline recombination in over half of 64 commonly used Cre driver lines, in most cases with a parental sex bias related to Cre expression in sperm or oocytes. Slight differences among Cre driver lines utilizing common transcriptional control elements affect germline recombination rates. Specific target loci demonstrated differential recombination; thus, reporters are not reliable proxies for another locus of interest. Similar principles apply to other recombinase systems and other genetically targeted organisms. We hereby draw attention to the prevalence of germline recombination and provide guidelines to inform future research for the neuroscience and broader molecular genetics communities.
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CITATIONS (153)
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