Abstract
We studied 3 Spanish patients with <1% FXII levels. DNA sequencing of the whole F12 gene identified 15 genetic variants. Molecular analyses of F12 mRNA demonstrated that the deficiency was caused by 5281delG in exon 9 of Patient 1 (in the homozygous state) and the 6306delG in exon 12 and another deletion of 23 bp in intron 8 of Patient 2 (both in the heterozygous state). Finally, a G-8C transversion was found in the homozygous state in Patient 3. Based on previous data, including a mouse model, the G-8C might be responsible for the FXII deficiency. None of these variants were present in 40 controls.Factor XII (FXII) participates in the blood coagulation cascade by initiating the intrinsic pathway, fibrinolysis, and generating bradykinin and angiotensin.1,2 FXII deficiency is a recessive Mendelian trait due to mutations in the F12 gene that comprises 14 exons on chromosome 5.3,4 The normal variation of FXII plasma levels exhibits a high heritability (67%) and is correlated significantly with thromboembolic disease.5 Despite the genetic data, the function of coagulation FXII is poorly understood and controversial results regarding the clinical consequences of variation in FXII levels have been described. While lower FXII levels have been associated with a high risk of arterial and venous thrombosis6 it has also been reported that patients with FXII deficiency may show no clinical symptoms. The present study examined the whole F12 gene in 3 patients with a severe FXII deficiency. Therefore, the genetic alterations in the F12, together with the co-segregation of the mutation C46T, may yield further understanding of the role of FXII and how it affects the risk of thrombosis.
Design and Methods
Subjects and blood samples
This study included 3 unrelated patients with severe FXII deficiency (<1%). Patient 1 was a 34 year old woman who had suffered 4 miscarriages within the first quarter of pregnancy. Patient 2 (I-1; Figure 1) was a 49 year old woman who had suffered one miscarriage in the second quarter of pregnancy. She had a family history of thromboembolic disease. We recruited her son (II-1; Figure 1) and daughter (II-2; Figure 1), 24 and 21 years old respectively. Patient 3 (II-2; Figure 2) was a 58 year old woman who had suffered an embolism at the age of 57. We also recruited her 2 sisters (II-1 and II-6; Figure 2), who were 60 and 51 years old, a 32 year old daughter (III-1; Figure 2) and 2 nieces (III-5 and III-7; Figure 2) 25 and 15 years of age respectively. No consanguinity among any of the patients’ parents was reported. All 3 patients exhibited normal values for the thrombophilic parameters (including functional antithrombin, amidolytic PC, total free and functional PS, functional assay for FVIII, APCR, the FVL, the G20210A F2, homocysteine levels, lupus anticoagulant, APTT test, anticardiolipin and antiphosphatidylserine antibodies) with the exception of prolonged APTT. All procedures were reviewed and approved by the Institutional Review Board of the Hospital de la Santa Creu i Sant Pau.
DNA and RNA analyses
DNA from the 3 patients and 40 healthy controls was isolated from peripheral blood leukocytes by a standard technique.7 We analyzed the F12 gene (including the promoter, exons, introns and the 3′-UTR) by PCR and direct sequencing of 4 overlapped fragments. The F12 gene DNA variants were determined in family members by independent sequencing analyses. RNA analyses were performed in 7 healthy individuals, in the 3 patients, in the offspring of Patient 2 and in 7 normal healthy controls. Total RNA was isolated from blood using the PAXgene Blood RNA kit following the supplier’s recommendations. Then, a RT-PCR was performed to obtain F12 cDNA. The F12 cDNA was sequenced as the genomic DNA. We used NetGene2 Server8 for the predictions of splice sites in humans. Genetic variants were numbered according to the transcription initiation.
Results and Discussion
We analyzed the whole F12 gene in 3 patients with severe FXII deficiency and 40 healthy controls. From these analyses we found that the F12 gene was 7,476 bp long rather than the 12 kb as previously described.3 This difference in length is due to intron 1 that contains 367 bp and not the 4677 bp that has been reported. This result was consistent in all of the individuals. To our knowledge, our study is the most extensive sequencing analysis that identified genetic variability in FXII-deficient families and it has allowed us to determine the correct sequence of the F12 locus. We identified 15 genetic variants in the F12 gene in the 3 patients (Table 1). It is worth noting that only 2 of the variants were located in exons and both were deletions. In addition, 11 out of the 15 DNA variants that we identified have not been published. In Patient 1, we found a G deletion at position 5281 in exon 9 (5281delG) in the homozygous state, affecting the codon 288 (confirmed as homozygous in the cDNA). Therefore, the pathologic effect could be attributable to the generation of a truncated protein by a premature stop codon (136 amino acids downstream than from wild type stop codon) in both alleles. In Patient 2 we found a heterozygous deletion of 23 bp in intron 8. This deletion (5081–5103del23bp) started 2 bp downstream from the end of exon 8 covering 27% of the intron 8. Some information on the function which of this mutation came from a bioinformatic analysis indicated that the presence of this deletion is consistent with the loss of both wild type donor and acceptor splice sites of intron 8 (Table 2). In addition, while there is no alternative donor splice site in the mutated sequence, a cryptic acceptor splice site sequence appeared 48 bp upstream than the wild type (Table 2) indicating that the surrounding sequences are important in selecting the new or the wild type acceptor sites. A second deletion (6306delG in exon 12) was found in Patient 2, introducing a frameshift that removed the wild type stop codon of the protein. Therefore, the resulting protein had 43 aminoacids more than the wild type protein. Since this deletion was found in the homozygous state in the cDNA but in the heterozygous state in the genomic DNA, it seemed that only the allele carrying this mutation was being expressed. The patient’s son and daughter (Figure 1) were heterozygous for each one of these deletions, which is in agreement with a heterozygous FXII deficiency in both individuals. In addition, although Patient 2 was homozygous for the normal allele (C/C) of the C46T mutation, both children were heterozygous having inherited the abnormal T allele from their father. The C46T mutation has been associated consistently with low FXII levels, therefore the co-existence of both mutations in these individuals (the deletion and the 46T), each mutation affecting a different allele, could explain the low (33%) FXII levels. Among the allelic variants found in Patient 3, only the mutations G-8C and T3292C were not detected in 40 unrelated controls. A relationship has been reported between severe FXII deficiency and these 2 mutations.9 As in this previous report, since our patient was also homozygous for both mutations, we cannot define their possible function. Nevertheless, Hofferbert9 suggested that the T3292C is responsible for the deficiency due to a cryptic splice site in intron 2, although expression analysis was not performed to confirm this hypothesis.9 In our study, when we analyzed the cDNA of Patient 3, no splicing change was observed. Therefore, it is unlikely that the intronic T3292C caused a FXII deficiency as a result of aberrant splicing. More importantly, it has been reported that HNF4-α transcription factor plays a critical role in the regulation of the expression of the F12 gene in the mouse.10 The binding site for HNF4-alpha in the promoter of F12 in the mouse (−64 AGACCTTTGCCCG-52) has a homologous binding site in the human F12 (−16 AGACCTTTGGCCA-4) that involved the G-8C mutation. This observation suggests that FXII deficiency in this patient was due to the reduction of expression by the modification of a transcription binding site. Nevertheless, further experiments and functional assays for this G-8C mutation should be performed to clarify its affect on FXII levels.
The sister and nieces of Patient 3 (Figure 2) were normal for the G-8C mutation, but her daughter (III-1; Figure 2) was heterozygous for this mutation, which is consistent with a heterozygous FXII deficiency (FXII levels of 67%). Of special interest is the difference observed in FXII levels in both nieces, since they share the same genotypes with the exception of C46T mutation. The III-7 is heterozygous for the C46T genotype (C/T) and showed FXII levels of 122%, whereas her sister (III-5) is homozygous for the mutated T allele. This shows a notable reduction of her FXII levels (62%). No other polymorphisms or mutations were identified in this branch of Patient 3’s family.
Based on our previous experience11 and although the F12 gene is expressed in liver, we took advantage of the ectopic transcription of F12 gene in lymphocyte to analyze the effect of these mutations at the mRNA levels. Our hypothesis was that the deletions and splice-site mutations identified in these patients might be responsible for the FXII deficiency by alterating the mRNA levels (alternative splicing or exon skipping). However, neither alteration in the mRNA processing nor other changes in the coding region were found in the cDNA from these patients.
There are only a few reports describing the molecular basis of congenital FXII deficiency. The majority of them deal with amino acid substitutions in the coding region.12–14 In our study, we did not detect any point mutation in the coding region, supporting the hypothesis that another kind of genetic variant (i.e., deletions) underlies the genetic basis of FXII deficiency. In addition, as reported in studies of other genes,11 the phenomenon of allelic exclusion could be a mechanism by which the F12 allele is not expressed resulting in the FXII deficiency. This mechanism by which a newly created premature termination codon results in a decrease in concentration of steady-state cytoplasmic mRNA is not yet understood.
In addition to these mutations, we detected the C46T mutation co-segregating in the patients and their families. Although the effect of this mutation on the FXII levels should be irrelevant in our patients due to the weighty effect of the rare mutations, the C46T mutation is clearly important in determining FXII levels in the patients’ relatives. In fact, although the members of these 2 families showed wide variability in FXII levels, the concentration of FXII in plasma were perfectly correlated with their respective genotypes, especially when the C46T genotype was taken into account.
An important issue to be addressed in our study is the clinical status of these patients. Two of them had suffered miscarriages (an expression of a thrombophilic condition) and one had a familial history of thrombosis. The third patient suffered a deep venous thrombosis. It is interesting to note that most of the patients with FXII deficiency and venous thrombosis had some associated congenital or acquired risk factors.15,16 In our study, with the exception of prolonged APTT, all 3 patients were normal for the basic thrombophilia parameters (including FVL and G20210A F2 mutations). Further studies, including follow-up of these families, should help clarify the role of FXII levels and the genetic determinants on the risk of cardiovascular disease. In conclusion, we believe that this molecular genetic study is a good illustration of the complexity of the relationship between phenotype and the risk of disease.
Acknowledgments
we are indebted to Professor W.H. Stone for his advice and helpful discussion
Footnotes
- Funding: this study was partially supported by grants PI-05/1361 and PI-05/1879 from FIS (Fondo de Investigación Sanitaria); and SAF2005–04738 (MCYT & FEDER). C. Mordillo Peñalba is involved in the Programa de Doctorado de Genética de la Universidad Autónoma de Barcelona (UAB). J.M. Soria was supported by Programa d’Estabilització d’Investigador de la Direcció d’Estrategia i Coordinació del Departament de Salut (Generalitat de Catalunya).
- Authors’ contributions JMS, JF, and CM designed the study. CM and EM-M performed experimental work. JMS and CM wrote the manuscript. All authors contributed to the interpretation of data, approved the final version of the manuscript and declared that they have no potential conflict if interest.
- Conflicts of Interest The authors reported no potential conflicts of interest.
- Received February 14, 2007.
- Accepted August 14, 2007.
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