Genome editing in K562 cells suggests a functional role for the XmnI Gg polymorphism: a widely used genetic marker in β-thalassemia and sickle cell disease patients.


Journal

Cellular and molecular biology (Noisy-le-Grand, France)
ISSN: 1165-158X
Titre abrégé: Cell Mol Biol (Noisy-le-grand)
Pays: France
ID NLM: 9216789

Informations de publication

Date de publication:
28 Jul 2024
Historique:
received: 29 04 2024
medline: 4 8 2024
pubmed: 4 8 2024
entrez: 4 8 2024
Statut: epublish

Résumé

The XmnI Gg -158 C/T polymorphism has been widely associated with fetal hemoglobin (HbF) levels, the severity of disease, and the response to the drug hydroxyurea (HU) in both β-thalassemia (β-thal) and sickle cell disease (SCD) patients. However, the functional significance of this single nucleotide polymorphism (SNP) remains unclear. To gain insight, green fluorescence protein (GFP) cassettes harboring the XmnI C or T alleles in their left homology arms (i.e. Gg promoters) were knocked into the Gg gene(s) of K562 cells via CRISPR/Cas9. Subsequently, the GFP fluorescence levels were compared in the ensuing cell populations and isolated clones. In both instances, median fluorescence intensities (MFI) of the knockin cells having the inserted XmnI T allele were higher than those having the XmnI C allele. Our results suggest that the XmnI T allele can increase Gg expression in K562 cells. The possible functional significance of the XmnI Gg -158 C/T polymorphism provides a rationale for the aforementioned associations. Furthermore, the XmnI polymorphism as a functional SNP substantiates its importance as a prognostic marker.

Identifiants

pubmed: 39097869
doi: 10.14715/cmb/2024.70.7.33
doi:

Substances chimiques

Genetic Markers 0
endodeoxyribonuclease XmnI EC 3.1.21.-
Deoxyribonucleases, Type II Site-Specific EC 3.1.21.4
Green Fluorescent Proteins 147336-22-9
Fetal Hemoglobin 9034-63-3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

230-236

Auteurs

Azadeh Ahmadifard (A)

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. azadeh.ahmadifard@gmail.com.

Nahal Maroofi (N)

Gene Therapy and Regenerative Medicine Research Center, Hope Generation Foundation, Tehran, Iran. nahal.maroofi@gmail.com.

Maryam Maleki Tehrani (M)

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. maryam.maleki28375@gmail.com.

Tahere Dabestani (T)

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. tdabestani@yahoo.com.

Masoumeh Sadat Mousavi Maleki (M)

Gene Therapy and Regenerative Medicine Research Center, Hope Generation Foundation, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. masmosavi@gmail.com.

Sepideh Bayrami (S)

Gene Therapy and Regenerative Medicine Research Center, Hope Generation Foundation, Tehran, Iran. bayramisepideh@gmail.com.

Mehdi Banan (M)

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. mbbanan@yahoo.com.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C

Classifications MeSH