48
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Gene-Targeted Mice

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common inherited disorder of mitochondrial fatty acid β-oxidation in humans. To better understand the pathogenesis of this disease, we developed a mouse model for MCAD deficiency (MCAD −/−) by gene targeting in embryonic stem (ES) cells. The MCAD −/− mice developed an organic aciduria and fatty liver, and showed profound cold intolerance at 4 °C with prior fasting. The sporadic cardiac lesions seen in MCAD −/− mice have not been reported in human MCAD patients. There was significant neonatal mortality of MCAD −/− pups demonstrating similarities to patterns of clinical episodes and mortality in MCAD-deficient patients. The MCAD-deficient mouse reproduced important aspects of human MCAD deficiency and is a valuable model for further analysis of the roles of fatty acid oxidation and pathogenesis of human diseases involving fatty acid oxidation.

          Synopsis

          Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is one of the most common inherited disorders of metabolism. This defect in fatty acid oxidation can lead to severe and sometimes fatal disease, especially in young children because they are unable to tolerate a fasting episode. Metabolic complications include very low blood glucose concentrations and generation of toxic by-products. This disorder can result in sudden infant death. Using a process known as gene targeting in mouse embryonic stem cells, the authors have developed a mouse model with the same enzyme deficiency. This mouse model of MCAD deficiency develops many of the same disease characteristics found in affected children. The MCAD-deficient mouse model shows a high rate of newborn loss, intolerance to cold, and the characteristic biochemical changes in the blood, tissues, and urine that are very similar to those found in the human disease counterpart. The MCAD-deficient mouse model will allow researchers to better understand disease mechanisms so that new preventive measures or therapies can be developed.

          Related collections

          Most cited references30

          • Record: found
          • Abstract: not found
          • Book: not found

          Molecular Cloning : A Laboratory Manual

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

            A new method of total RNA isolation by a single extraction with an acid guanidinium thiocyanate-phenol-chloroform mixture is described. The method provides a pure preparation of undegraded RNA in high yield and can be completed within 4 h. It is particularly useful for processing large numbers of samples and for isolation of RNA from minute quantities of cells or tissue samples.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Altering the genome by homologous recombination.

              M Capecchi (1989)
              Homologous recombination between DNA sequences residing in the chromosome and newly introduced, cloned DNA sequences (gene targeting) allows the transfer of any modification of the cloned gene into the genome of a living cell. This article discusses the current status of gene targeting with particular emphasis on germ line modification of the mouse genome, and describes the different methods so far employed to identify those rare embryonic stem cells in which the desired targeting event has occurred.
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                pgen
                PLoS Genetics
                Public Library of Science (San Francisco, USA )
                1553-7390
                1553-7404
                August 2005
                19 August 2005
                : 1
                : 2
                : e23
                Affiliations
                [1 ] Department of Genetics, University of Alabama, Birmingham, Alabama, United States of America
                [2 ] Department of Comparative Medicine, Stanford University, Stanford, California, United States of America
                [3 ] Department of Medical Genetics, Mayo Clinic College of Medicine, Rochester, Minnesota, United States of America
                [4 ] Division of Medical Genetics, Children's Hospital, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America
                [5 ] Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, Minnesota, United States of America
                Johns Hopkins Institute, United States of America
                Author notes
                *To whom correspondence should be addressed. E-mail: paw@ 123456uab.edu
                Article
                05-PLGE-RA-0058R2 plge-01-02-07
                10.1371/journal.pgen.0010023
                1189074
                16121256
                78d030bf-6987-478d-85a1-eb56f8c77c7d
                Copyright: © 2005 Tolwani et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 29 March 2005
                : 1 July 2005
                Categories
                Research Article
                Genetics/Disease Models
                Mus (Mouse)
                Custom metadata
                Tolwani RJ, Hamm DA, Tian L, Sharer JD, Vockley J, et al. (2005) Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted mice. PLoS Genet 1(2): e23.

                Genetics
                Genetics

                Comments

                Comment on this article