ADAMTS13 gene; a novel splicing site mutation in a case with thrombotic thrombocytopenic purpura

Implication for health policy/practice/research/medical education: The c.2728C>T (p.Arg910X) mutation in ADAMTS13 gene was found in a patient with congenital TTP. Moreover, we found c.2610+5G>A mutation, a novel splicing variant, that affects exon 20 and encodes for the ADAMTS13’s thrombospondin type-1 fifth domain in this case. This novel variant expected to cause aberrant ADAMTS13 transcript processing. Please cite this paper as: Zununi Vahed S, Cremaschi A, Zaker B, Rasi Hashemi SS, Ardalan M. ADAMTS13 gene; a novel splicing site mutation in a case with thrombotic thrombocytopenic purpura. J Nephropharmacol. 2021;10(2):x-x. DOI: 10.34172/ npj.2021.17. A plasma protease, ADAMTS13, cleaves the von Willebrand factor (VWF) and its deficiency is associated with the pathogenesis of thrombotic thrombocytopenic purpura (TTP). According to the Human Gene Mutation Database (HGMD), about 150 mutations have been identified in the ADAMTS13 gene. A 23-year-old man, with hematuria and gingival bleeding was admitted to our University Hospital. Four years ago he was diagnosed with a TTP history. During these years, he was under intermittent plasma exchange. A blood sample was taken for genetic study. He effectively responded to one session of fresh frozen plasma replacement and plasma exchange. Genetic study indicated that this case carries two heterozygous mutations in ADAMTS13 gene; a novel splicing variant (c.2610+5G>A) and a nonsense p.Arg910X mutation that previously is reported to relate to TTP. The novel variant predicted to result in an aberrant ADAMTS13 transcript processing. A R T I C L E I N F O


Introduction
Thrombotic thrombocytopenic purpura (TTP) is identified by small-vessel platelet-rich thrombi and presents with microangiopathic hemolytic anemia, thrombocytopenia, and consequent multiorgan dysfunction (1). Deficiency of a plasma protease ADAMTS13 cleaving the von Willebrand factor (VWF), can result in VWF perseverance that plays an important role in the pathogenesis of TTP (2). ADAMTS13 deficiency is determined by either genetic causes (congenital TTP) or by autoantibodies against the protease (acquired TTP). Congenital TTP, responsible for less than 5% of cases (3,4), is an autosomal recessive disorder (2) due to compound heterozygous or homozygous mutations in the ADAMTS13 gene, which is located on chromosome 9.
According to the Human Gene Mutation Database (HGMD), about 150 mutations of the ADAMTS13 gene have been recognized so far. They included: 113 missense/ nonsense mutations, 10 splicing mutations (Table 1), 21 small deletions, 7 small insertions, and 5 gross deletions.
In this report, we describe a case of a young male from Iran suffers from congenital TTP and carries two heterozygous mutations in ADAMTS13 gene: a novel splicing variant (c.2610+5G>A) and a nonsense p.Arg910X mutation that previously is reported to associate with TTP. The novel variant predicted to result in an aberrant ADAMTS13 transcript processing.

Case Report
A 23-year-old man, with hematuria and gingival bleeding was admitted to our University Hospital. Four years he was diagnosed with a clinical history of TTP. After TTP was diagnosed, he received intermittent sessions of plasmapheresis (once a week) for one year. Urinalysis revealed hematuria and peripheral blood examination disclosed schistocytes. The laboratory findings at the time of admission presented in Table 2. ADAMTS13 enzyme activity was less than 10% during active disease. We did not measure the autoantibody titer of ADAMTS13. The patient received 2 liter per day plasmapheresis with fresh frozen plasma (FFP) replacement and after clinical improvement (platelet count >100 000/mm 3 , lactate dehydrogenase (LDH) <600 (units/L)), he was discharged. Thereafter, he was under our frequent follow up and still now he is receiving once weekly plasma exchange (2 liters per session).
DNA was extracted from the patient's peripheral blood cells and genetic analysis was performed at Mario Negri Institute for Pharmacological Research in Bergamo (Italy). DNA from healthy parents and siblings was not available for genotyping.
All coding exons and flanking intronic regions of the ADAMTS13 gene were analyzed by Sanger sequencing. We recognized a heterozygous mutation, located at exon 21, leading to the insertion of a premature stop codon (c.2728C>T, NM_139025.4, p.Arg910X). This mutation is absent in public databases (dbSNP151, 1000 Genomes Project, Exome Aggregation Consortium, The Genome Aggregation Database), but it has been previously reported in a case of TTP with childhood onset (2). We identified a second heterozygous mutation (c.2610+5G>A) laying in intron 20, predicted to probably affect the splicing of exon 20. This variant has been reported neither in public databases nor in TTP patients. In silico analyses predicted that the possibility of the exon 20 correct splicing declines from 0.983 to 0 versus the wild-type sequence (GenScan software) (5) in the mutant sequence. Furthermore, an aberrant exon 20 characterized by the retention of 21-base pairs was predicted with a probability of 0.572, leading to an in-frame insertion of 7 amino acids (VNALGMR) in the protein sequence.
Additional predictions with the Human Splicing Finder software (6) confirmed that this mutation causes the break of the wild-type donor splicing site.

Discussion
Here, we describe the clinical course of a patient with congenital TTP in whom we identified the underlying genetic abnormality. The c.2728C>T (p.Arg910X) mutation found in our patient was previously reported and its functional effect was shown. However, the c.2610+5G>A mutation, which affects exon 20 and encodes for the ADAMTS13's thrombospondin type-1 fifth domain, is novel. As shown, it is predicted to interfere with normal ADAMTS13 mRNA splicing but future studies are needed to confirm the functional effect of this substitution. An accurate splicing of pre-mRNA is a serious stage in protein translation and posttranscriptional regulation. Consensus "cis-acting" splicing sequences existence in exon-intron boundaries is essential for recognition by splicing machinery. By creating new splicing sites, splicing regulatory sequences, disruption of existing splice sites, or activating the cryptic splicing sites,    (7). Congenital TTP is an autosomal recessive disorder. Thus, mutations have to affect both alleles of ADAMTS13. Unfortunately, DNA from patient's parents was not available to assess the segregation of the c.2728C>T and the c.2610+5G>A. However, his ADAMTS13 activity was less than 10%, leading us to reasonably assume that the two mutations are carried on different chromosomes, and to speculate that the c.2610+5G>A disrupts the correct splicing of ADAMTS13 transcript.