A A386g biallelic GPIbα gene mutation with anomalous behavior

A new mechanism suggested for Bernard-Soulier syndrome pathogenesis

Silvia Vettore, Fabiana Tezza, Alessandro Malara, Fabrizio Vianello, Alessandro Pecci, Raffaella Scandellari, Matteo Floris, Alessandra Balduini, Fabrizio Fabris

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Platelet glycoprotein GPIbα mutations are the basic defect behind Bernard-Soulier syndrome, a rare inherited macrothrombocytopenia characterized by anomalies of the GPIbα, GPIbb and GPIX subunits of von Willebrand factor receptor. A 32-year old man was investigated for suspected Bernard-Soulier syndrome. Ristocetin induced agglutination was absent. Flow cytometry and Western blot analysis showed a severe reduction in GPIbα, but sequencing revealed only a biallelic c.386A>G substitution, theoretically leading to a p.Asn110Glu variation. To further clarify the data, megakaryocyte cultures were set. Though the maturation of megakaryocytes was normal, proplatelet formation was defective and GPIbα mRNA was not detectable. GPIX protein was slightly reduced and GPIbb polypeptide almost absent. Computational analysis showed that the c.386A>G mutation disrupted an exon splicing enhancer motif involved in the proper maturation of the GPIbα transcript. The c.386A>G mutation suggests a unique mutational mechanism causing the virtual absence of GPIbα without creating a stop codon.

Original languageEnglish
Pages (from-to)1878-1882
Number of pages5
JournalHaematologica
Volume96
Issue number12
DOIs
Publication statusPublished - Dec 1 2011

Fingerprint

Bernard-Soulier Syndrome
Megakaryocytes
Mutation
Ristocetin
Genes
Platelet Membrane Glycoproteins
Terminator Codon
Agglutination
Exons
Flow Cytometry
Western Blotting
Messenger RNA
Peptides
Proteins

Keywords

  • Bernard-soulier
  • Congenital thrombocytopenia
  • Glycoprotein Ibα
  • Platelets

ASJC Scopus subject areas

  • Hematology

Cite this

A A386g biallelic GPIbα gene mutation with anomalous behavior : A new mechanism suggested for Bernard-Soulier syndrome pathogenesis. / Vettore, Silvia; Tezza, Fabiana; Malara, Alessandro; Vianello, Fabrizio; Pecci, Alessandro; Scandellari, Raffaella; Floris, Matteo; Balduini, Alessandra; Fabris, Fabrizio.

In: Haematologica, Vol. 96, No. 12, 01.12.2011, p. 1878-1882.

Research output: Contribution to journalArticle

Vettore, S, Tezza, F, Malara, A, Vianello, F, Pecci, A, Scandellari, R, Floris, M, Balduini, A & Fabris, F 2011, 'A A386g biallelic GPIbα gene mutation with anomalous behavior: A new mechanism suggested for Bernard-Soulier syndrome pathogenesis', Haematologica, vol. 96, no. 12, pp. 1878-1882. https://doi.org/10.3324/haematol.2010.039008
Vettore, Silvia ; Tezza, Fabiana ; Malara, Alessandro ; Vianello, Fabrizio ; Pecci, Alessandro ; Scandellari, Raffaella ; Floris, Matteo ; Balduini, Alessandra ; Fabris, Fabrizio. / A A386g biallelic GPIbα gene mutation with anomalous behavior : A new mechanism suggested for Bernard-Soulier syndrome pathogenesis. In: Haematologica. 2011 ; Vol. 96, No. 12. pp. 1878-1882.
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