GM21068
LCL from B-Lymphocyte
Description:
HOLOCARBOXYLASE SYNTHETASE DEFICIENCY
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Heritable Diseases |
Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
|
Tissue Type
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Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
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LCL from B-Lymphocyte
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Race
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White
|
Family Member
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1
|
Relation to Proband
|
proband
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Confirmation
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Clinical summary/Case history
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin confirmed by LINE assay |
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biotin--[propionyl-CoA-carboxylase (ATP-hydrolyzing)] ligase |
According to the submitter biochemical test results for this subject showed decreased enzyme activity. EC Number: 6.3.4.10 |
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propionyl-CoA carboxylase |
According to the submitter biochemical test results for this subject showed decreased enzyme activity. EC Number: 6.4.1.3 |
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pyruvate carboxylase |
According to the submitter biochemical test results for this subject showed decreased enzyme activity. EC Number: 6.4.1.1 |
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methylcrotonyl-CoA carboxylase |
According to the submitter biochemical test results for this subject showed decreased enzyme activity. EC Number: 6.4.1.4 |
|
Remarks |
Clinically affected; product of a twin pregnancy; holocarboxylase synthetase deficient; acidosis; "cat urine" odor; shock; responded well to biotin treatment; mother was given supplemental biotin in the last trimester of pregnancy due to history of two previously affected infants; deficient propionyl CoA carboxylase, pyruvate carboxylase, and B-methylcrotonyl CoA carboxylase; see GM03522 Fibroblast |
Roth KS, Allan L, Yang W, Foreman JW, Dakshinamurti K, Serum and urinary biotin levels during treatment of holocarboxylase synthetase deficiency. Clin Chim Acta109:337-40 1981 |
PubMed ID: 7226522 |
|
Roth KS, Yang W, Foremann JW, Rothman R, Segal S, Holocarboxylase synthetase deficiency: a biotin-responsive organic acidemia. J Pediatr96:845-9 1980 |
PubMed ID: 7365583 |
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Roth K, Cohn R, Yandrasitz J, Preti G, Dodd P, Segal S, Beta-methylcrotonic aciduria associated with lactic acidosis The Journal of pediatrics88:229-35 1976 |
PubMed ID: 1249684 |
Split Ratio |
1:2 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not Inactivated |
Substrate |
None specified |
Subcultivation Method |
dilution - add fresh medium |
Supplement |
- |
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