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Citations to this article

Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation.
M L Raff, … , F D Ledley, D S Rosenblatt
M L Raff, … , F D Ledley, D S Rosenblatt
Published January 1, 1991
Citation Information: J Clin Invest. 1991;87(1):203-207. https://doi.org/10.1172/JCI114972.
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Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation.

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Abstract

Genetic complementation of fibroblasts from patients with methylmalonic aciduria (MMA) defines a unique class of allelic mutations arising from mutations at the locus encoding the methylmalonyl coenzyme A (CoA) mutase apoenzyme. Various phenotypes of MMA have been delineated including complete absence of enzyme activity (mut0) and abnormal enzyme activity with an elevated Km for adenosylcobalamin (mut-). We describe genetic studies on a cell line (WG1130) from a patient with mut0 MMA which exhibited an unusual complementation phenotype, complementing with three of nine mut0 cell lines and four of five mut- cell lines. This suggests that interallelic complementation occurs between mutant alleles in WG1130 and subsets of alleles associated with both mut0 and mut- phenotypes. The methylmalonyl CoA mutase cDNA was cloned from WG1130 and found to contain a G354----A (Arg93----His) mutation. Gene transfer of this mutant clone into primary fibroblasts from patients with MMA confirms that this mutation expresses a mut0 phenotype when transferred into a mut0 cell line with low levels of mRNA but can contribute to apoenzyme function when transferred into mut cell lines which show correction with WG1130 by somatic cell complementation. These results point to further heterogeneity within both mut0 and mut- and may enable identification of mutations affecting discrete components of apoenzyme function.

Authors

M L Raff, A M Crane, R Jansen, F D Ledley, D S Rosenblatt

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Year: 2021 2019 2016 2015 2014 2010 2007 2006 2005 2003 1998 1997 1996 1995 1994 1993 1992 1991 Total
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Citations to this article (31)

Title and authors Publication Year
MUT gene variants in patients with methylmalonic acidemia in Bangladeshi population and their distinguishing metabolic profiles
R Begum, AA Sajib, AB Islam, SK Sarker, MS Islam, N Saha, K Mannoor, F Qadri, S Akhteruzzaman
Meta Gene 2021
A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia
L Kang, Y Liu, M Shen, Y Liu, R He, J Song, Y Jin, M Li, Y Zhang, H Dong, X Liu, H Yan, J Qin, H Zheng, Y Chen, D Li, H Wei, H Zhang, L Sun, Z Zhu, D Liang, Y Yang
Journal of Inherited Metabolic Disease 2019
Mutation analysis of genes related to methylmalonic acidemia: identification of eight novel mutations
F Keyfi, MR Abbaszadegan, M Sankian, A Rolfs, S Orolicki, M Pournasrollah, M Alijanpour, A Varasteh
Molecular Biology Reports 2019
Molecular Genetic Characterization of 151 Mut -Type Methylmalonic Aciduria Patients and Identification of 41 Novel Mutations in MUT
P Forny, AS Schnellmann, C Buerer, S Lutz, B Fowler, DS Froese, MR Baumgartner
Human Mutation 2016
Clinical features and MUT gene mutation spectrum in Chinese patients with isolated methylmalonic acidemia: identification of ten novel allelic variants
LS Han, Z Huang, F Han, J Ye, WJ Qiu, HW Zhang, Y Wang, ZW Gong, XF Gu
World Journal of Pediatrics 2015
JIMD Reports
A Khanna, R Gish, SC Winter, WL Nyhan, BA Barshop
JIMD reports 2015
Correction of Methylmalonic Aciduria In Vivo Using a Codon-Optimized Lentiviral Vector
ES Wong, C McIntyre, HL Peters, E Ranieri, DS Anson, JM Fletcher
Human Gene Therapy 2014
JIMD Reports
F Imtiaz, BM Al-Mubarak, A Al-Mostafa, M Al-Hamed, R Allam, Z Al-Hassnan, M Al-Owain, H Al-Zaidan, Z Rahbeeni, A Qari, EA Faqeih, A Alasmari, F Al-Mutairi, M Alfadhel, WM Eyaid, MS Rashed, M Al-Sayed
JIMD reports 2014
Genetic disorders of vitamin B12 metabolism: eight complementation groups – eight genes
DS Froese, RA Gravel
Expert Reviews in Molecular Medicine 2010
Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductase
CL Elmore, X Wu, D Leclerc, ED Watson, T Bottiglieri, NI Krupenko, SA Krupenko, JC Cross, R Rozen, RA Gravel, RG Matthews
Molecular Genetics and Metabolism 2007
Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes
RJ Chandler, MS Tsai, K Dorko, J Sloan, M Korson, R Freeman, S Strom, CP Venditti
BMC Medical Genetics 2007
Spectrum of mutations inmutmethylmalonic acidemia and identification of a common Hispanic mutation and haplotype
LC Worgan, K Niles, JC Tirone, A Hofmann, A Verner, A Sammak, T Kucic, P Lepage, DS Rosenblatt
Human Mutation 2006
Three novel and six common mutations in 11 patients with methylmalonic acidemia
A Kobayashi, H Kakinuma, H Takahashi
Pediatrics International 2006
Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut° and mut- forms of methylmalonic acidemia: Identification of 29 novel mutations in the MUT gene
C Acquaviva, JF Benoist, S Pereira, I Callebaut, T Koskas, D Porquet, J Elion
Human Mutation 2005
Lexikon der Syndrome und Fehlbildungen
R Witkowski, O Prokop, E Ullrich, G Thiel
2003
A common mutation among blacks with mut− methylmalonic aciduria
CE Adjalla, AR Hosack, NV Matiaszuk, DS Rosenblatt
Human Mutation 1998
Expression of Normal and Mutant Pyruvate Dehydrogenase Complex E1α cDNAs in Cultured Human Lymphoblasts
K Chun, BH Robinson
Archives of Biochemistry and Biophysics 1998
Principles of Perinatal—Neonatal Metabolism
RM Cowett
1998
Mutations inmut methylmalonic acidemia: Clinical and enzymatic correlations
FD Ledley, DS Rosenblatt
Human Mutation 1997
Homology modeling of human methylmalonyl-CoA mutase: A structural basis for point mutations causing methylmalonic aciduria
NH Thomä, PF Leadlay
Protein Science 1996
Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthase
CL Drennan, RG Matthews, DS Rosenblatt, FD Ledley, WA Fenton, ML Ludwig
Proceedings of the National Academy of Sciences 1996
A 13-bp deletion (1952 del 13) in the methylmalonyl CoA mutase gene of an affected patient
RL Touraine, MO Rolland, P Divry, M Mathieu, P Guibaud, D Bozon
Human Mutation 1995
Cloning and expression of mutations demonstrating intragenic complementation in mut0 methylmalonic aciduria
AA Qureshi, AM Crane, NV Matiaszuk, I Rezvani, FD Ledley, DS Rosenblatt
Journal of Clinical Investigation 1994
Inherited disorders of cobalamin metabolism
AA Qureshi, DS Rosenblatt, BA Cooper
Critical Reviews in Oncology/Hematology 1994
Mutations participating in interallelic complementation in propionic acidemia
RA Gravel, BR Akerman, AM Lamhonwah, M Loyer, A Léon-del-Rio, I Italiano
The American Journal of Human Genetics 1994
Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia
AM Crane, FD Ledley
The American Journal of Human Genetics 1994
Varying neurological phenotypes amongmut° andmut− patients with methylmalonylCoA mutase deficiency
MI Shevell, N Matiaszuk, FD Ledley, DS Rosenblatt
American Journal of Medical Genetics 1993
Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduria
AM Crane, R Jansen, ER Andrews, FD Ledley
Journal of Clinical Investigation 1992
Propionate metabolism in cultured human cells after overexpression of recombinant methylmalonyl CoA mutase: Implications for somatic gene therapy
M Wilkemeyer, J Stankovics, T Foy, FD Ledley
Somatic Cell and Molecular Genetics 1992
Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutase
AM Crane, LS Martin, D Valle, FD Ledley
Human Genetics 1992
Ketoacidotic crisis as a presentation of mild (“benign”) methylmalonic acidemia
SK Shapira, FD Ledley, DS Rosenblatt, HL Levy
The Journal of Pediatrics 1991

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