FIELD: biotechnology.
SUBSTANCE: invention relates to biotechnology, in particular to a method for creating a genetically engineered mouse model of pigmented autosomal recessive retinitis having a deletion of two nucleotides in the second exon of the pde6b gene, which encodes the β-subunit of cyclic guanidine monphosphate phosphodiesterase, by disabling the pde6b gene. Method includes a guide RNA mixture microinjection, which is complementary to the pde6b gene second exon, capable of forming a complex with the effector protein Cas9 and hybridizing with the target sequence of the pde6b gene, and the Cas9 protein into a mouse zygote, setting the zygotes after microinjection into the uterus of a pseudo pregnant female mouse, genotoping the resulting mice, and breeding a line of mice that are homozygous due to the pde6b gene knockout.
EFFECT: invention provides for efficiently obtaining a directed deletion of 2 nucleotides in the second exon of the pde6b gene leading to a reading frame shift in the translation of the gene and gene disabling.
1 cl, 3 dwg
Title | Year | Author | Number |
---|---|---|---|
METHOD FOR EDITING THE GJB2 GENE TO CORRECT THE PATHOGENIC VARIANT OF c.del35G IN HUMAN CELLS CULTURED IN VITRO | 2021 |
|
RU2780677C1 |
GENE EDITING OF DEEP INTRON MUTATIONS | 2016 |
|
RU2759335C2 |
METHODS FOR PROTECTION OF PIG FETUSES FROM VIRUS INFECTION | 2018 |
|
RU2778405C2 |
TECHNOLOGY FOR OBTAINING MICE WITH A HUMANIZED GNAO1 REGION IN THE REGION OF SINGLE NUCLEOTIDE POLYMORPHISM rs587777057 FOR TESTING RNA THERAPY FOR GNAO1 c.607 G>A PATIENTS | 2021 |
|
RU2757121C1 |
METHOD FOR OBTAINING A MOUSE MODEL FOR STUDYING LESCH-NYHAN SYNDROME BY INTRODUCING A DELETION OF P.Val8del INTO THE Hprtl GENE | 2021 |
|
RU2768048C1 |
METHOD FOR PRODUCING GENETICALLY MODIFIED LABORATORY ANIMALS WITH NULL ALLELE OF P2rx3 GENE | 2022 |
|
RU2805173C1 |
METHOD OF PRODUCING GENETICALLY MODIFIED MICE EXPRESSING HUMAN ANTITHROMBIN III MINIGENE USING MICROINJECTIONS OF TELN-LINEARIZED DNA FRAGMENT | 2022 |
|
RU2806568C1 |
METHODS AND COMPOSITIONS FOR THE TREATMENT OF DISORDERS AND DISEASES RELATED TO RDH12 | 2017 |
|
RU2764920C2 |
DELIVERY AND USE OF SYSTEMS OF CRISPR-CAS, VECTORS AND COMPOSITIONS FOR TARGETED ACTION AND THERAPY IN LIVER | 2014 |
|
RU2716420C2 |
GENETIC CONSTRUCT CONTAINING CHIMERIC GUIDE RNA SEQUENCES FOR DELETION OF HUMAN SMN1 GENE IN HUMAN CELL CULTURES | 2022 |
|
RU2816897C2 |
Authors
Dates
2023-03-13—Published
2022-02-07—Filed