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Clinical presentation and proteomic signature of patients with TANGO2 mutations.

ABSTRACT: Transport And Golgi Organization protein 2 (TANGO2) deficiency has recently been identified as a rare metabolic disorder with a distinct clinical and biochemical phenotype of recurrent metabolic crises, hypoglycemia, lactic acidosis, rhabdomyolysis, arrhythmias, and encephalopathy with cognitive decline. We report nine subjects from seven independent families, and we studied muscle histology, respiratory chain enzyme activities in skeletal muscle and proteomic signature of fibroblasts. All nine subjects carried autosomal recessive TANGO2 mutations. Two carried the reported deletion of exons 3 to 9, one homozygous, one heterozygous with a 22q11.21 microdeletion inherited in trans. The other subjects carried three novel homozygous (c.262C>T/p.Arg88*; c.220A>C/p.Thr74Pro; c.380+1G>A), and two further novel heterozygous (c.6_9del/p.Phe6del); c.11-13delTCT/p.Phe5del mutations. Immunoblot analysis detected a significant decrease of TANGO2 protein. Muscle histology showed mild variation of fiber diameter, no ragged-red/cytochrome c oxidase-negative fibers and a defect of multiple respiratory chain enzymes and coenzyme Q₁₀ (CoQ₁₀ ) in two cases, suggesting a possible secondary defect of oxidative phosphorylation. Proteomic analysis in fibroblasts revealed significant changes in components of the mitochondrial fatty acid oxidation, plasma membrane, endoplasmic reticulum-Golgi network and secretory pathways. Clinical presentation of TANGO2 mutations is homogeneous and clinically recognizable. The hemizygous mutations in two patients suggest that some mutations leading to allele loss are difficult to detect. A combined defect of the respiratory chain enzymes and CoQ₁₀ with altered levels of several membrane proteins provides molecular insights into the underlying pathophysiology and may guide rational new therapeutic interventions.

SUBMITTER: Mingirulli N

PROVIDER: S-EPMC7078914 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

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Clinical presentation and proteomic signature of patients with TANGO2 mutations.

Mingirulli Nadja N Pyle Angela A Hathazi Denisa D Alston Charlotte L CL Kohlschmidt Nicolai N O'Grady Gina G Waddell Leigh L Evesson Frances F Cooper Sandra B T SBT Turner Christian C Duff Jennifer J Topf Ana A Yubero Delia D Jou Cristina C Nascimento Andrés A Ortez Carlos C García-Cazorla Angels A Gross Claudia C O'Callaghan Maria M Santra Saikat S Preece Maryanne A MA Champion Michael M Korenev Sergei S Chronopoulou Efsthatia E Anirban Majumdar M Pierre Germaine G McArthur Daniel D Thompson Kyle K Navas Placido P Ribes Antonia A Tort Frederic F Schlüter Agatha A Pujol Aurora A Montero Raquel R Sarquella Georgia G Lochmüller Hanns H Jiménez-Mallebrera Cecilia C Taylor Robert W RW Artuch Rafael R Kirschner Janbernd J Grünert Sarah C SC Roos Andreas A Horvath Rita R

Journal of inherited metabolic disease 20190813 2

Transport And Golgi Organization protein 2 (TANGO2) deficiency has recently been identified as a rare metabolic disorder with a distinct clinical and biochemical phenotype of recurrent metabolic crises, hypoglycemia, lactic acidosis, rhabdomyolysis, arrhythmias, and encephalopathy with cognitive decline. We report nine subjects from seven independent families, and we studied muscle histology, respiratory chain enzyme activities in skeletal muscle and proteomic signature of fibroblasts. All nine ...[more]

PMID: 31339582

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Clinical presentation and proteomic signature of patients with TANGO2 mutations.

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Clinical presentation and proteomic signature of patients with TANGO2 mutations.

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