A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect

Silvia Vettore, Daniela De Rocco, Bernhard Gerber, Raffaella Scandellari, Anna Monica Bianco, Carlo L. Balduini, Alessandro Pecci, Fabrizio Fabris, Anna Savoia

Research output: Contribution to journalArticle

Abstract

MYH9-related disease ( MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, the gene encoding the heavy chain of non-muscle myosin IIA. Patients present with congenital macrothrombocytopenia and inclusion bodies in neutrophils and might develop sensorineural deafness, presenile cataract, and/or progressive nephropathy leading to end-stage renal failure. In two families with macrothrombocytopenia we identified a novel c.3485G > C mutation in the last nucleotide of exon 25. Bioinformatic tools for splice site prediction and minigene functional test predicted splicing anomalies of exon 25. However, analysis of RNA purified from patient's peripheral blood did not allowed us to detect any anomalies, suggesting that RNA processing is correct at least in this tissue. Therefore, we concluded that c.3485G > C leads to a novel missense mutation (p.Arg1162Thr) of myosin-9, which resulted to be slightly degraded in patient platelets. A precise definition of the effect of mutations is fundamental to improve our knowledge into the pathogenetic mechanisms responsible for the disease.

Original languageEnglish
Pages (from-to)256-260
Number of pages5
JournalEuropean Journal of Medical Genetics
Volume53
Issue number5
DOIs
Publication statusPublished - Sep 2010

Fingerprint

Missense Mutation
Exons
Nucleotides
Mutation
Nonmuscle Myosin Type IIA
RNA
Genes
Inclusion Bodies
Deafness
Myosins
Computational Biology
Cataract
Chronic Kidney Failure
Neutrophils
Blood Platelets

Keywords

  • Macrothrombocytopenia
  • Missense and splicing mutation
  • MYH9 gene
  • MYH9-related disease
  • Neutrophil inclusion

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

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title = "A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect",
abstract = "MYH9-related disease ( MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, the gene encoding the heavy chain of non-muscle myosin IIA. Patients present with congenital macrothrombocytopenia and inclusion bodies in neutrophils and might develop sensorineural deafness, presenile cataract, and/or progressive nephropathy leading to end-stage renal failure. In two families with macrothrombocytopenia we identified a novel c.3485G > C mutation in the last nucleotide of exon 25. Bioinformatic tools for splice site prediction and minigene functional test predicted splicing anomalies of exon 25. However, analysis of RNA purified from patient's peripheral blood did not allowed us to detect any anomalies, suggesting that RNA processing is correct at least in this tissue. Therefore, we concluded that c.3485G > C leads to a novel missense mutation (p.Arg1162Thr) of myosin-9, which resulted to be slightly degraded in patient platelets. A precise definition of the effect of mutations is fundamental to improve our knowledge into the pathogenetic mechanisms responsible for the disease.",
keywords = "Macrothrombocytopenia, Missense and splicing mutation, MYH9 gene, MYH9-related disease, Neutrophil inclusion",
author = "Silvia Vettore and {De Rocco}, Daniela and Bernhard Gerber and Raffaella Scandellari and Bianco, {Anna Monica} and Balduini, {Carlo L.} and Alessandro Pecci and Fabrizio Fabris and Anna Savoia",
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T1 - A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect

AU - Vettore, Silvia

AU - De Rocco, Daniela

AU - Gerber, Bernhard

AU - Scandellari, Raffaella

AU - Bianco, Anna Monica

AU - Balduini, Carlo L.

AU - Pecci, Alessandro

AU - Fabris, Fabrizio

AU - Savoia, Anna

PY - 2010/9

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N2 - MYH9-related disease ( MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, the gene encoding the heavy chain of non-muscle myosin IIA. Patients present with congenital macrothrombocytopenia and inclusion bodies in neutrophils and might develop sensorineural deafness, presenile cataract, and/or progressive nephropathy leading to end-stage renal failure. In two families with macrothrombocytopenia we identified a novel c.3485G > C mutation in the last nucleotide of exon 25. Bioinformatic tools for splice site prediction and minigene functional test predicted splicing anomalies of exon 25. However, analysis of RNA purified from patient's peripheral blood did not allowed us to detect any anomalies, suggesting that RNA processing is correct at least in this tissue. Therefore, we concluded that c.3485G > C leads to a novel missense mutation (p.Arg1162Thr) of myosin-9, which resulted to be slightly degraded in patient platelets. A precise definition of the effect of mutations is fundamental to improve our knowledge into the pathogenetic mechanisms responsible for the disease.

AB - MYH9-related disease ( MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, the gene encoding the heavy chain of non-muscle myosin IIA. Patients present with congenital macrothrombocytopenia and inclusion bodies in neutrophils and might develop sensorineural deafness, presenile cataract, and/or progressive nephropathy leading to end-stage renal failure. In two families with macrothrombocytopenia we identified a novel c.3485G > C mutation in the last nucleotide of exon 25. Bioinformatic tools for splice site prediction and minigene functional test predicted splicing anomalies of exon 25. However, analysis of RNA purified from patient's peripheral blood did not allowed us to detect any anomalies, suggesting that RNA processing is correct at least in this tissue. Therefore, we concluded that c.3485G > C leads to a novel missense mutation (p.Arg1162Thr) of myosin-9, which resulted to be slightly degraded in patient platelets. A precise definition of the effect of mutations is fundamental to improve our knowledge into the pathogenetic mechanisms responsible for the disease.

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