Literature DB >> 34622318

[Genomics and proteomics in the research of neuromuscular diseases].

Andrea Gangfuß1, Ulrike Schara-Schmidt1, Andreas Roos2,3.   

Abstract

Neurological diseases affect 3-5% of children and, apart from cardiovascular diseases and cancer, represent the most prominent cause of morbidity and mortality in adults and particularly in the aged population of western Europe. Neuromuscular disorders are a subgroup of neurological diseases and often have a genetic origin, which leads to familial clustering. Despite the enormous progress in the analysis of the genome, such as by sequence analysis of coding regions of deoxyribonucleic acid or even the entire deoxyribonucleic acid sequence, in approximately 50% of the patients suffering from rare forms of neurological diseases the genetic cause remains unsolved. The reasons for this limited detection rate are presented in this article. If a treatment concept is available, under certain conditions this can have an impact on the adequate and early treatment of these patients. Considering neuromuscular disorders as a paradigm, this article reports on the advantages of the inclusion of next generation sequencing analysis-based DNA investigations as an omics technology (genomics) and the advantage of the integration with protein analyses (proteomics). A special focus is on the combination of genomics and proteomics in the sense of a proteogenomic approach in the diagnostics and research of these diseases. Along this line, this article presents a proteogenomic approach in the context of a multidisciplinary project aiming towards improved diagnostic work-up and future treatment of patients with neuromuscular diseases; "NMD-GPS: gene and protein signatures as a global positioning system in patients suffering from neuromuscular diseases".
© 2021. Springer Medizin Verlag GmbH, ein Teil von Springer Nature.

Entities:  

Keywords:  Genetic origin; Muscle proteomics; Next generation sequencing analysis; Omics technology; Proteogenomics

Mesh:

Year:  2021        PMID: 34622318     DOI: 10.1007/s00115-021-01201-1

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  5 in total

Review 1.  Mass spectrometry-based protein analysis to unravel the tissue pathophysiology in Duchenne muscular dystrophy.

Authors:  Stephanie J Carr; René P Zahedi; Hanns Lochmüller; Andreas Roos
Journal:  Proteomics Clin Appl       Date:  2017-07-13       Impact factor: 3.494

2.  Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.

Authors:  Joachim Schessl; Yaqun Zou; Meagan J McGrath; Belinda S Cowling; Baijayanta Maiti; Steven S Chin; Caroline Sewry; Roberta Battini; Ying Hu; Denny L Cottle; Michael Rosenblatt; Lynn Spruce; Arupa Ganguly; Janbernd Kirschner; Alexander R Judkins; Jeffrey A Golden; Hans-Hilmar Goebel; Francesco Muntoni; Kevin M Flanigan; Christina A Mitchell; Carsten G Bönnemann
Journal:  J Clin Invest       Date:  2008-03       Impact factor: 14.808

Review 3.  Intersection of Proteomics and Genomics to "Solve the Unsolved" in Rare Disorders such as Neurodegenerative and Neuromuscular Diseases.

Authors:  Andreas Roos; Rachel Thompson; Rita Horvath; Hanns Lochmüller; Albert Sickmann
Journal:  Proteomics Clin Appl       Date:  2017-10-23       Impact factor: 3.494

4.  INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH.

Authors:  Denisa Hathazi; Dan Cox; Adele D'Amico; Giorgio Tasca; Richard Charlton; Robert-Yves Carlier; Jennifer Baumann; Laxmikanth Kollipara; René P Zahedi; Ingo Feldmann; Jean-Francois Deleuze; Annalaura Torella; Ronald Cohn; Emily Robinson; Francesco Ricci; Heinz Jungbluth; Fabiana Fattori; Anne Boland; Emily O'Connor; Rita Horvath; Rita Barresi; Hanns Lochmüller; Andoni Urtizberea; Marie-Line Jacquemont; Isabelle Nelson; Laura Swan; Gisèle Bonne; Andreas Roos
Journal:  Brain       Date:  2021-09-04       Impact factor: 13.501

  5 in total

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