Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects

Marcin M. Gorski, Anna Lecchi, Eti A. Femia, Silvia La Marca, Andrea Cairo, Emanuela Pappalardo, Luca A. Lotta, Andrea Artoni, Flora Peyvandi

Research output: Contribution to journalArticle

Abstract

Primary platelet secretion defects constitute a heterogeneous group of functional defects characterized by reduced platelet granule secretion upon stimulation by different agonists. The clinical and laboratory heterogeneity of primary platelet secretion defects warrants a tailored approach. We performed a pilot study in order to develop DNA sequence analysis pipelines for gene discovery and to create a list of candidate causal genes for platelet secretion defects. Whole-exome sequencing analysis of 14 unrelated Italian patients with primary secretion defects and 16 controls was performed on Illumina HiSeq. Variant prioritization was carried out using two filtering approaches: identification of rare, potentially damaging variants in platelet candidate genes or by selecting singletons. To corroborate the results, exome sequencing was applied in a family in which platelet secretion defects and a bleeding diathesis were present. Platelet candidate gene analysis revealed gene defects in 10/14 patients, which included ADRA2A, ARHGAP1, DIAPH1, EXOC1, FCGR2A, ITPR1, LTBP1, PTPN7, PTPN12, PRKACG, PRKCD, RAP1GAP, STXBP5L, and VWF. The analysis of singletons identified additional gene defects in PLG and PHACTR2 in two other patients. The family analysis confirmed a missense variant p.D1144N in the STXBP5L gene and p.P83H in the KCNMB3 gene as potentially causal. In summary, exome sequencing revealed potential causal variants in 12 of 14 patients with primary platelet secretion defects, highlighting the limitations of the genomic approaches for causal gene identification in this heterogeneous clinical and laboratory phenotype.

Original languageEnglish
Pages (from-to)2084-2090
Number of pages7
JournalHaematologica
Volume104
Issue number10
DOIs
Publication statusPublished - Jan 1 2019

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Exome
Genetic Association Studies
Blood Platelets
Genes
Disease Susceptibility
DNA Sequence Analysis
Hemorrhage
Phenotype

ASJC Scopus subject areas

  • Hematology

Cite this

Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects. / Gorski, Marcin M.; Lecchi, Anna; Femia, Eti A.; La Marca, Silvia; Cairo, Andrea; Pappalardo, Emanuela; Lotta, Luca A.; Artoni, Andrea; Peyvandi, Flora.

In: Haematologica, Vol. 104, No. 10, 01.01.2019, p. 2084-2090.

Research output: Contribution to journalArticle

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