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Generation of Fel d 1 chain 2 genome-edited cats by CRISPR-Cas9 system.


ABSTRACT: Allergens from domestic cats (Felis catus) cause allergy-related health problems worldwide. Fel d 1 is a major allergen that causes severe allergic reactions in humans, including rhinitis, conjunctivitis, and life-threatening asthma. Therefore, patients with cat allergies anticipate hypoallergenic cats. We successfully generated Fel d 1 chain 2 (CH2) genome-edited cats using the CRISPR-Cas9 system in this study. T7 endonuclease 1 assay and Sanger sequencing were used to confirm the mutation in CH2 genome-edited cats. Fel d 1 level in CH2 genome-edited cats were assessed by enzyme-linked immunosorbent assay (ELISA). Remarkably, ELISA showed that the level of Fel d 1 in the CH2 homozygous genome-edited cat (Name: Alsik) was extremely low compared with that in wild type domestic cats and could be hypoallergenic cats. Additionally, we successfully cloned the CH2 homozygous genome-edited cat using cytoplasm injection clone technology. The cloned CH2 homozygous genome-edited cat was verified using microsatellite analysis. Creating hypoallergenic cats using the CRISPR-Cas9 system is a significant step forward because these cats can safely approach allergic patients.

SUBMITTER: Lee SR 

PROVIDER: S-EPMC10904870 | biostudies-literature | 2024 Feb

REPOSITORIES: biostudies-literature

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Generation of Fel d 1 chain 2 genome-edited cats by CRISPR-Cas9 system.

Lee Sang Ryeul SR   Lee Kyung-Lim KL   Song Seok-Hwan SH   Joo Myeong-Don MD   Lee Seo-Hyun SH   Kang Ji-Su JS   Kang Seon-Min SM   Idrees Muhammad M   Kim Jae-Wook JW   Kong Il-Keun IK  

Scientific reports 20240229 1


Allergens from domestic cats (Felis catus) cause allergy-related health problems worldwide. Fel d 1 is a major allergen that causes severe allergic reactions in humans, including rhinitis, conjunctivitis, and life-threatening asthma. Therefore, patients with cat allergies anticipate hypoallergenic cats. We successfully generated Fel d 1 chain 2 (CH2) genome-edited cats using the CRISPR-Cas9 system in this study. T7 endonuclease 1 assay and Sanger sequencing were used to confirm the mutation in C  ...[more]

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