Literature DB >> 1980486

Structure of the human methylmalonyl-CoA mutase (MUT) locus.

S U Nham1, M F Wilkemeyer, F D Ledley.   

Abstract

The MUT locus encoding the enzyme methylmalonyl-CoA mutase is defective in mut forms of methylmalonic acidemia. This locus has been mapped to chromosome 6p12-21.1. We report cloning and characterization of this locus which comprises 13 exons spanning greater than 35 kb of the genome. The MUT locus exhibits consensus sequences for transcription, splicing, and polyadenylation. The putative promoter region was localized in a CG island 5' to exon I and was shown to direct expression of a beta-galactosidase reporter gene in cultured cells. Of interest is the observation that the first intron occurs within the 5' untranslated region, and no introns separate the mitochondrial targeting sequences and the mature apoenzyme. An informative HindIII polymorphism was localized within the coding sequence and can be assayed using the polymerase chain reaction. These studies describe the structure of the MUTlocus and provide a foundation for characterization of mutations in mut methylmalonic acidemia.

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Year:  1990        PMID: 1980486     DOI: 10.1016/0888-7543(90)90259-w

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  14 in total

Review 1.  Role of vitamin B12 on methylmalonyl-CoA mutase activity.

Authors:  Tóshiko Takahashi-Iñiguez; Enrique García-Hernandez; Roberto Arreguín-Espinosa; María Elena Flores
Journal:  J Zhejiang Univ Sci B       Date:  2012-06       Impact factor: 3.066

2.  Clinical characteristics and gene mutation analysis of methylmalonic aciduria.

Authors:  Qin Yi; Juanjuan Lv; Fengyan Tian; Hong Wei; Qin Ning; Xiaoping Luo
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2011-06-14

3.  Methylmalonic Acidemia Diagnosis by Laboratory Methods.

Authors:  Fatemeh Keyfi; Saeed Talebi; Abdol-Reza Varasteh
Journal:  Rep Biochem Mol Biol       Date:  2016-10

4.  Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation.

Authors:  M L Raff; A M Crane; R Jansen; F D Ledley; D S Rosenblatt
Journal:  J Clin Invest       Date:  1991-01       Impact factor: 14.808

Review 5.  The management and outcome of propionic and methylmalonic acidaemia.

Authors:  J V Leonard
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

6.  Refining the map and defining flanking markers of the gene for autosomal recessive polycystic kidney disease on chromosome 6p21.1-p12.

Authors:  G Mücher; B Wirth; K Zerres
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

7.  Mutation Analyses in Selected Exons of the MUT Gene in Indian Patients with Methylmalonic Acidemia.

Authors:  Chandrawati Kumari; Seema Kapoor; Bijo Varughese; Sunil Kumar Pollipali; Siddarth Ramji
Journal:  Indian J Clin Biochem       Date:  2016-08-04

8.  Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia.

Authors:  Faiqa Imtiaz; Bashayer M Al-Mubarak; Abeer Al-Mostafa; Mohamed Al-Hamed; Rabab Allam; Zuhair Al-Hassnan; Mohammed Al-Owain; Hamad Al-Zaidan; Zuhair Rahbeeni; Alya Qari; Eissa Ali Faqeih; Ali Alasmari; Fuad Al-Mutairi; Majid Alfadhel; Wafaa M Eyaid; Mohamed S Rashed; Moeenaldeen Al-Sayed
Journal:  JIMD Rep       Date:  2015-11-29

9.  Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutase.

Authors:  A M Crane; L S Martin; D Valle; F D Ledley
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

10.  Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia.

Authors:  A M Crane; F D Ledley
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

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