Literature DB >> 33823724

ETF dehydrogenase advances in molecular genetics and impact on treatment.

Sara Missaglia1,2, Daniela Tavian1,2, Corrado Angelini3.   

Abstract

Electron transfer flavoprotein dehydrogenase, also called ETF-ubiquinone oxidoreductase (ETF-QO), is a protein localized in the inner membrane of mitochondria, playing a central role in the electron-transfer system. Indeed, ETF-QO mediates electron transport from flavoprotein dehydrogenases to the ubiquinone pool. ETF-QO mutations are often associated with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (RR-MADD, OMIM#231680), a multisystem genetic disease characterized by various clinical manifestations with different degrees of severity. In this review, we outline the clinical features correlated with ETF-QO deficiency and the benefits obtained from different treatments, such as riboflavin, L-carnitine and/or coenzyme Q10 supplementation, and a diet poor in fat and protein. Moreover, we provide a detailed summary of molecular and bioinformatic investigations, describing the mutations identified in ETFDH gene and highlighting their predicted impact on enzymatic structure and activity. In addition, we report biochemical and functional analysis, performed in HEK293 cells and patient fibroblasts and muscle cells, to show the relationship between the nature of ETFDH mutations, the variable impairment of enzyme function, and the different degrees of RR-MADD severity. Finally, we describe in detail 5 RR-MADD patients carrying different ETFDH mutations and presenting variable degrees of clinical symptom severity.

Entities:  

Keywords:  ETF-QO; lipid storage myopathy; multiple acyl-CoA dehydrogenase deficiency; phenotype–genotype correlation; riboflavin treatment

Year:  2021        PMID: 33823724     DOI: 10.1080/10409238.2021.1908952

Source DB:  PubMed          Journal:  Crit Rev Biochem Mol Biol        ISSN: 1040-9238            Impact factor:   8.250


  5 in total

1.  Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin Tribe.

Authors:  Orna Staretz-Chacham; Shirly Amar; Shlomo Almashanu; Ben Pode-Shakked; Ann Saada; Ohad Wormser; Eli Hershkovitz
Journal:  Genes (Basel)       Date:  2021-07-28       Impact factor: 4.096

2.  Generation and network analysis of an RNA-seq transcriptional atlas for the rat.

Authors:  Kim M Summers; Stephen J Bush; Chunlei Wu; David A Hume
Journal:  NAR Genom Bioinform       Date:  2022-03-07

3.  Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects.

Authors:  Antonino Lupica; Rosaria Oteri; Sara Volta; Daniele Ghezzi; Selene Francesca Anna Drago; Carmelo Rodolico; Olimpia Musumeci; Antonio Toscano
Journal:  Front Neurol       Date:  2022-03-03       Impact factor: 4.003

4.  S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome.

Authors:  Fuying Chen; Cheng Ni; Xiaoxiao Wang; Ruhong Cheng; Chaolan Pan; Yumeng Wang; Jianying Liang; Jia Zhang; Jinke Cheng; Y Eugene Chin; Yi Zhou; Zhen Wang; Yiran Guo; She Chen; Stephanie Htun; Erin F Mathes; Alejandra G de Alba Campomanes; Anne M Slavotinek; Si Zhang; Ming Li; Zhirong Yao
Journal:  EMBO Mol Med       Date:  2022-04-01       Impact factor: 14.260

5.  Role of RNA in Molecular Diagnosis of MADD Patients.

Authors:  Célia Nogueira; Lisbeth Silva; Ana Marcão; Carmen Sousa; Helena Fonseca; Hugo Rocha; Teresa Campos; Elisa Leão Teles; Esmeralda Rodrigues; Patrícia Janeiro; Ana Gaspar; Laura Vilarinho
Journal:  Biomedicines       Date:  2021-05-04
  5 in total

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