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Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism
Year:
2012
Source of publication :
Diabetes
Authors :
Laiba, Efrat
;
.
Volume :
61
Co-Authors:
Shemer, R., Department of Developmental Biology and Cancer Research, Faculty of Medicine, Hebrew University, Jerusalem, Israel
Ziv, C.A., Division of Pediatric Endocrinology, Department of Pediatrics, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Laiba, E., Division of Pediatric Endocrinology, Department of Pediatrics, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Zhou, Q., Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, OR, United States
Gay, J., Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, OR, United States
Tunovsky-Babaey, S., Endocrinology and Metabolism Service, Internal Medicine Department, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Shyng, S.-L., Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, OR, United States
Glaser, B., Endocrinology and Metabolism Service, Internal Medicine Department, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Zangen, D.H., Division of Pediatric Endocrinology, Department of Pediatrics, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Facilitators :
From page:
258
To page:
263
(
Total pages:
6
)
Abstract:
Congenital hyperinsulinism (CHI) is most commonly caused by mutations in the β-cell ATP-sensitive K + (KATP) channel genes. Severe CHI was diagnosed in a 1-day-old girl; the mother's cousin and sister had a similar phenotype. ABCC8 gene sequencing (leukocyte DNA) revealed a heterozygous, exon 37, six-base pair inframe insertion mutation in the affected patient and aunt but also in her unaffected mother and grandfather. In expression studies using transfected COSm6 cells, mutant sulfonylurea receptor 1 (SUR1) protein was expressed on the cell surface but failed to respond to MgADP even in the heterozygous state. mRNA expression in lymphocytes determined by sequencing cDNA clones and quantifying 6FAM-labeled PCR products found that although the healthy mother predominantly expressed the normal transcript, her affected daughter, carrying the same mutant allele, primarily transcribed the mutant. The methylation pattern of the imprinting control region of chromosome 11p15.5 and ABCC8 promoter was similar for all family members. In conclusion, differences in transcript expression may determine the clinical phenotype of CHI in this maternally inherited dominant mutation. The use of peripheral lymphocytes as a peripheral window to the β-cell transcription profile can serve in resolving β-cell phenotypes. The severe, dominant-negative nature of the 1508insAS mutation suggests that it affects the functional stoichiometry of SUR1-regulated gating of K ATP channels. © 2012 by the American Diabetes Association.
Note:
Related Files :
adenosine triphosphate
Base Sequence
Female
gene expression
genetic analysis
phenotype
protein abcc8
Show More
Related Content
More details
DOI :
10.2337/db11-0984
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
19439
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:29
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Scientific Publication
Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism
61
Shemer, R., Department of Developmental Biology and Cancer Research, Faculty of Medicine, Hebrew University, Jerusalem, Israel
Ziv, C.A., Division of Pediatric Endocrinology, Department of Pediatrics, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Laiba, E., Division of Pediatric Endocrinology, Department of Pediatrics, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Zhou, Q., Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, OR, United States
Gay, J., Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, OR, United States
Tunovsky-Babaey, S., Endocrinology and Metabolism Service, Internal Medicine Department, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Shyng, S.-L., Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, OR, United States
Glaser, B., Endocrinology and Metabolism Service, Internal Medicine Department, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Zangen, D.H., Division of Pediatric Endocrinology, Department of Pediatrics, Hadassah Hebrew University Medical Center, Jerusalem, Israel
Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism
Congenital hyperinsulinism (CHI) is most commonly caused by mutations in the β-cell ATP-sensitive K + (KATP) channel genes. Severe CHI was diagnosed in a 1-day-old girl; the mother's cousin and sister had a similar phenotype. ABCC8 gene sequencing (leukocyte DNA) revealed a heterozygous, exon 37, six-base pair inframe insertion mutation in the affected patient and aunt but also in her unaffected mother and grandfather. In expression studies using transfected COSm6 cells, mutant sulfonylurea receptor 1 (SUR1) protein was expressed on the cell surface but failed to respond to MgADP even in the heterozygous state. mRNA expression in lymphocytes determined by sequencing cDNA clones and quantifying 6FAM-labeled PCR products found that although the healthy mother predominantly expressed the normal transcript, her affected daughter, carrying the same mutant allele, primarily transcribed the mutant. The methylation pattern of the imprinting control region of chromosome 11p15.5 and ABCC8 promoter was similar for all family members. In conclusion, differences in transcript expression may determine the clinical phenotype of CHI in this maternally inherited dominant mutation. The use of peripheral lymphocytes as a peripheral window to the β-cell transcription profile can serve in resolving β-cell phenotypes. The severe, dominant-negative nature of the 1508insAS mutation suggests that it affects the functional stoichiometry of SUR1-regulated gating of K ATP channels. © 2012 by the American Diabetes Association.
Scientific Publication
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