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BioMed Research International
Volume 2014 (2014), Article ID 256245, 8 pages
A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy
1Laboratoire de Génomique Biomédicale et Oncogénétique (LR 11 IPT 05), Institut Pasteur de Tunis, Université de Tunis El Manar, El Manar I, BP 74, 13 Place Pasteur 1002 Tunis Belvédère, 2092 Tunis, Tunisia
2Département de Dermatologie, Hôpital Charles Nicolle de Tunis, 1006 Tunis, Tunisia
3Département d’Anatomie-Pathologique Humaine et Expérimentale, Institut Pasteur de Tunis, 1002 Tunis, Tunisia
4Département d’Oncologie Médicale, Hôpital Abderrahman Mami, 2080 Ariana, Tunisia
5Département d’Oncologie Médicale, Hôpital La Rabta de Tunis, 1007 Tunis, Tunisia
Received 22 February 2014; Accepted 23 March 2014; Published 4 May 2014
Academic Editor: Margit Burmeister
Copyright © 2014 Mariem Ben Rekaya et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Xeroderma pigmentosum Variant (XP-V) form is characterized by a late onset of skin symptoms. Our aim is the clinical and genetic investigations of XP-V Tunisian patients in order to develop a simple tool for early diagnosis. We investigated 16 suspected XP patients belonging to ten consanguineous families. Analysis of the POLH gene was performed by linkage analysis, long range PCR, and sequencing. Genetic analysis showed linkage to the POLH gene with a founder haplotype in all affected patients. Long range PCR of exon 9 to exon 11 showed a 3926 bp deletion compared to control individuals. Sequence analysis demonstrates that this deletion has occurred between two Alu-Sq2 repetitive sequences in the same orientation, respectively, in introns 9 and 10. We suggest that this mutation POLH NG_009252.1: g.36847_40771del3925 is caused by an equal crossover event that occurred between two homologous chromosomes at meiosis. These results allowed us to develop a simple test based on a simple PCR in order to screen suspected XP-V patients. In Tunisia, the prevalence of XP-V group seems to be underestimated and clinical diagnosis is usually later. Cascade screening of this founder mutation by PCR in regions with high frequency of XP provides a rapid and cost-effective tool for early diagnosis of XP-V in Tunisia and North Africa.
Xeroderma pigmentosum (XP) is an autosomal recessive cancer prone disease characterized by sensitivity to ultraviolet rays (UVR). XP patients are consequently predisposed to develop skin and eyes cancers . This disease is caused by inherited mutations in DNA repair genes encoding proteins that protect cells from UV-induced damage. XP is genetically heterogeneous with seven XP complementation groups (XP-A to XP-G) defective in nucleotide excision repair (NER) pathway and an additional “variant” form (XP-V) with normal NER but a deficient translesional synthesis.
XP-V patients have a relatively milder phenotype with a late onset of symptoms and delayed progression. Typically, XP-V patients do not have ocular or neurological abnormalities . Many studies suggest that this form of XP is underdiagnosed [3, 4]. Therefore, XP-V patients represent only 20 to 30% of all XP cases .
Cells from XP-V patients are extremely hypermutable after exposure to UV due to the deficiency of pol eta [6, 7]. The DNA polymerase eta () normally catalyzes translesion synthesis (TLS) by incorporating dAMP opposite thymine residues of a cyclobutane thymine dimer (CPD) [8, 9]. In the absence of pol eta, the highly error-prone pol iota undertakes this bypass function resulting in the accumulation of UV-induced mutations and an increase in the susceptibility to skin cancer [10, 11].
Pol eta is encoded by the POLH gene, the human homolog of yeast Rad30 . Pol plays an important role in preventing genome instability after UV or cisplatin-induced DNA damage . Chemoresistance of cancer to cisplatin treatment is due in part to human Pol . Crystal structures of hPol complexed with intrastrand cisplatin identified a hydrophobic pocket as a potential drug target for reducing chemoresistance .
More than 60 mutations have been identified in the POLH gene in cell lines derived from XP-V patients from different geographic locations, mainly Russia-Armenia, Scotland, Lebanon, Iran, Belgium, France, Japan, USA, Europe, Asia, Cayman Islands, Turkey, Israel, Germany, Korea, Algeria, and Tunisia [2–4, 9, 14–23].
In our study, we surveyed POLH mutations in 16 Tunisian patients with late onset of XP in order to assess the causative mutations of this disorder and to develop a rapid molecular diagnostic test.
2. Patients and Methods
Sixteen suspected XP-V patients belonging to ten consanguineous Tunisian families originated from different regions of Tunisia were investigated (Table 2). Their age was ranging from 4 to 50 years.
Written informed consent was obtained from all available family members or from parents of minor children. Families were interviewed using a structured questionnaire to collect information about family history, consanguinity, affected members, and associated diseases. DNA was isolated from peripheral blood leukocyte using salting-out method  or Qiagen kit DNA extraction.
2.2.1. Genetic Analysis
To confirm linkage to POLH gene, available family members were genotyped using two polymorphic microsatellite markers spanning a 0.4 Mb interval near to POLH locus (cen-D6S207 and D6S1582 (POLH-)tel) as previously described . Microsatellite markers were selected from the genetic maps available on NCBI browsers and the CEPH genotype database (http://www.cephb.fr/en/cephdb/) on the basis of their heterozygosity percentage and closeness to the POLH gene. Genotyping was performed as described elsewhere .
2.2.2. PCR Long-Range
On absence of amplification of POLH exon 10, long PCR was performed using the Expand Long Template PCR System Kit (Expand Long Range dNTPack 700 units/μL Roche). PCR was performed using different primers (Table 3). The PCR program included 92°C for 2 min, 10 cycles of 92°C for 10 sec, 60°C for 15 sec, 68°C for 10 min, and 20 cycles of the same program except that the extension step was extended by 20 sec per cycle. PCR products were run on 1% agarose gel with the DNA ladder 1 kb molecular size marker (GeneRulerTM).
2.2.3. Bioinformatic Analysis
As several genomic rearrangements are commonly caused by recombination events induced by repetitive elements present in the human genome, the genomic sequence of the POLH gene (NG_009252.1) was obtained and analyzed from chr6: 43578281 to 43581387 position corresponding to exon 9 to exon 11 region. Screening for repetitive elements was performed using the RepeatMasker software available at http://www.repeatmasker.org/ (Table 1).
2.2.4. Sequencing and Mutation Analysis
Long range PCR products were directly sequenced using the ABI 3130 Genetic Analyzer by two pairs of primers (Table 3). Mutation analysis and breakpoints of the deletion were determined as the last nucleotide showing sequence identity between wild and mutated sequences (Figure 3).
2.2.5. Mutation Nomenclature
The genomic reference of the POLH gene NG_011763.1 was used to annotate the deletion according to the HGVS version 2.0 (Mutalyzer 2.0.beta-26).
3.1. Clinical Findings
In this study, we investigated sixteen patients with late onset of XP features. These patients belong to ten consanguineous families from different Tunisian geographic areas (Table 2). For all patients, skin hyperphotosensitivity to UVR began at a mean age of 4 years. The mean age at onset of the first skin cancer was 24 years. Nonmelanoma skin cancer (NMSC) occurred in only 10 patients. At least, 3 among them developed only basal cell carcinoma (BCC) and 5 developed squamous cell carcinoma (SCC) combined with BCC (Table 2).
3.2. Genetic Analysis
The genetic examination of XP-V patients was initially assessed through routine procedures, which involved genotyping of all consanguineous XP-V patients and available related individuals. Haplotype analysis showed homozygosity for the closest two markers to POLH gene, D6S1582 and D6S271, with a founder haplotype (129–188) in all investigated patients (Figure 1).
3.3. PCR Long-Range
DNA samples from these patients repeatedly failed to yield PCR amplification products for exon 10. Therefore, we assumed the presence of a genomic deletion spanning exon 10 (del exon 10). As del exon 10 was previously described in Italian patient at the genomic DNA level with 2.7 Kb deletion , we first screen for this deletion. Therefore, screening of this deletion by PCR did not yield any amplification product confirming that there are different breakpoints involved in our XP-V patients. In order to identify the deletion size, we amplified the sequence between exon 9 and exon 11 using primers POLH10ΔF and POLH10ΔR showed in Table 3. Long range PCR revealed kb product for XP-V patients versus ≈10 kb in control individual corresponding to approximately 4 kb size deletion (Figure 2).
3.4. Bioinformatic Analysis
Screening of repetitive elements present in exon 9 to exon 11 using repeat masker software revealed that 51.44% (4814 pb) of the sequence was interspersed repeat sequences. Among them, 11 SINE Alu sequences spanned a region of 2908 bp (31.08% of all the sequence) and 3 LINE sequences spanned a region of 1789 bp (19.12% of all the sequence). These Alu sequences are predicted to promote the occurrence of large deletions (Table 1).
3.5. Mutation Screening
In order to detect the breakpoints with accuracy, two internal primer pairs were designed to sequence introns 9 and 10 across the deletion (Table 3). Direct sequencing and analysis of the 6 kb PCR product (Figure 2) of XPV17 and XPV91 patients using primers POLHdelF and POLHdelR revealed that both the 5′ and 3′ breakpoints were located within homologous Alu Sq2 (class SINE (short interspersed elements, family Alu)) elements in introns 9 and 10 of POLH gene (Figure 3). This deletion POLH NG_009252.1: g.32438_36363del3926led to the loss of exon 10 (c.1370-2567_1539+1188del3925). This mutation has likely resulted from Alu-Alu equal homologous recombination.
3.6. Screening of Deletion by PCR
After identification of the deletion breakpoints in two patients (XPV91 and XPV17), we screened the following patients for this deletion by PCR using primers POLHdelF and POLHdelR showed in Table 3. In all patients, we found a product of 500 pb versus 4500 pb in virtual PCR. We then confirmed the presence of the same breakpoints by direct sequencing.
For individuals at a heterozygous state, we confirmed their profiles by two PCRs. The presence of one allele of exon 10 was confirmed using XPV10F and XPV10R primers and the absence of exon 10 on the other allele was confirmed using POLHdelF and POLHdelR primers.
We report 16 cases with NMSC, BCC, and SCC that occurred with a mean delay of 24 years after XP diagnosis. Five of our patients (XPV6KE, XP18G XPV20G, XPV43-1, and XPV53Z) had been treated by skin radiotherapy (Table 2). After cancer treatment, many NMSC appeared. For example, XPV6KE died after frontal tumor metastasis and XPV18G experienced a metastasis after recurrence on the right cheek. These consequences may be explained by the significant role of pol eta in cancer radiotherapy response. Pol eta-deficient cells are resistant to ionizing radiation. This radioresistance results from the increased reparation of double strand breaks by homologous recombination repair system (HR) . While for chemotherapy, previous studies demonstrate that pol eta-deficient cells are very sensitive to cisplatin and oxaliplatin and particularly for agents which exert their activities by blocking DNA replication forks . Among the roles of pol eta is repairing lesions induced by cisplatin. Consequently, systemic chemotherapy using cisplatin will attack healthy cells and induce novel cancers on absence of pol eta. This type of chemotherapy may be very dangerous for XP-V patients. Knowing this important role of pol eta, mutation screening of POLH gene in patients with SCC or BCC could have an impact in guiding treatment choice.
Previous studies showed two specific mutations (c.1568_1571delGTCA and c.660+1G>A) in three XP-V Tunisian patients [4, 20]. Deletion of exon 10 has been previously described at the cDNA level in XP-V patients from different geographic origins. It was found at homozygous state in two Algerian (XP62VI and XP75VI) and in one American (XP139DC) and at heterozygous state in one Tunisian (XP28VI) XP-V patients [3, 16]. Also, POLH del exon 10 has been described at genomic level in one Italian patient with 2.7 Kb deletion occurring between two poly (T) sequences  and in one Algerian XP-V patient with 3.763 bp deletion . We report here a novel breakpoint of del exon 10, POLH NG_009252.1: g.32438_36363del3926, that presents in 16 XP-V Tunisian patients belonging to 10 unrelated families. This deletion can be screened by a simple PCR without confirming by sequencing. This rapid tool may facilitate molecular investigation of XP-V patient.
This mutation is probably a founder variation because it was carried by a particular haplotype (129–188 or 129–186). Del exon 10 is common in the world and probably it may be due to different founder effects. Repetitive sequences are the primary candidates to generate stable abnormal secondary structures producing large deletion during replication . Alu elements are normally located within introns and 3′ untranslated regions of genes, which are considered mutational “hotspots” for large gene rearrangements . Large deletions in POLH gene have been previously described in exons 5 and 6 [3, 16]. Similar founder mutations in the POLH gene have been reported in other populations such as Japanese and Korean. Therefore, 87% of the Japanese XP-V patients shared one of the four founder mutations described in Japan [3, 18].
The presence of this founder mutation, reported in our study, could simplify genetic screening of XP patients in Tunisian population by implementing presymptomatic tests and hence early UV protection. Before treatment of patients’ skin cancers, XP status should be verified to avoid cancer recurrence. It is also important to consider the possible existence of such large deletion at heterozygous state. Consequently, we propose systematic screening of this mutation in all XP-V patients by two PC reactions; the 1st will amplify exon 10, while the 2nd will amplify across deletion breakpoints. After confirmation at a large scale in XP Tunisian patients, the test will be proposed for patients from Southern Mediterranean and Middle East countries.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors would like to thank the patients and their families as well as the patients’ support group “Helping Xeroderma Pigmentosum Children” (http://www.xp-tunisie.org.tn/) for their collaboration. This work was supported by the Tunisian Ministry of Higher Education and Scientific Research (Laboratory on Biomedical Genomics and Oncogenetics, no. LR 11 IPT 05) and the Tunisian Ministry of Public Health.
- K. H. Kraemer, N. J. Patronas, R. Schiffmann, B. P. Brooks, D. Tamura, and J. J. DiGiovanna, “Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship,” Neuroscience, vol. 145, no. 4, pp. 1388–1396, 2007.
- A. Gratchev, P. Strein, J. Utikal, and G. Sergij, “Molecular genetics of Xeroderma pigmentosum variant,” Experimental Dermatology, vol. 12, no. 5, pp. 529–536, 2003.
- H. Inui, K. S. Oh, C. Nadem et al., “Xeroderma pigmentosum-variant patients from America, Europe, and Asia,” Journal of Investigative Dermatology, vol. 128, no. 8, pp. 2055–2068, 2008.
- M. B. Rekaya, O. Messaoud, A. Mebazaa et al., “A novel POLH gene mutation in a Xeroderma pigmentosum-V Tunisian patient: phenotype-genotype correlation,” Journal of Genetics, vol. 90, no. 3, pp. 483–487, 2011.
- S. Moriwaki and K. H. Kraemer, “Xeroderma pigmentosum—bridging a gap between clinic and laboratory,” Photodermatology Photoimmunology and Photomedicine, vol. 17, no. 2, pp. 47–54, 2001.
- P. Kannouche and A. Stary, “Xeroderma pigmentosum variant and error-prone DNA polymerases,” Biochimie, vol. 85, no. 11, pp. 1123–1132, 2003.
- A. Stary, P. Kannouche, A. R. Lehmann, and A. Sarasin, “Role of DNA polymerase η in the UV mutation spectrum in human cells,” The Journal of Biological Chemistry, vol. 278, no. 21, pp. 18767–18775, 2003.
- C. Masutani, M. Araki, A. Yamada et al., “Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity,” EMBO Journal, vol. 18, no. 12, pp. 3491–3501, 1999.
- C. Masutani, R. Kusumoto, A. Yamada et al., “The XPV (Xeroderma pigmentosum variant) gene encodes human DNA polymerase η,” Nature, vol. 399, no. 6737, pp. 700–704, 1999.
- C. A. Dumstorf, A. B. Clark, Q. Lin et al., “Participation of mouse DNA polymerase ι in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 48, pp. 18083–18088, 2006.
- Q. Gueranger, A. Stary, S. Aoufouchi et al., “Role of DNA polymerases η, ι and ζ in UV resistance and UV-induced mutagenesis in a human cell line,” DNA Repair, vol. 7, no. 9, pp. 1551–1562, 2008.
- S. Cruet-Hennequart, K. Gallagher, A. M. Sokòl, S. Villalan, A. M. Prendergast, and M. P. Carty, “DNA polymerase η, a key protein in translesion synthesis in human cells,” Sub-Cellular Biochemistry, vol. 50, pp. 189–209, 2010.
- Y. Zhao, C. Biertumpfel, M. T. Gregory, Y. J. Hua, F. Hanaoka, and W. Yang, “Structural basis of human DNA polymerase η-mediated chemoresistance to cisplatin,” Proceedings of the National Academy of Sciences of the United States of America, vol. 109, no. 19, pp. 7269–7274, 2012.
- T. Itoh and S. Linn, “XP43TO, previously classified as Xeroderma pigmentosum group E, should be reclassified as Xeroderma pigmentosum variant,” Journal of Investigative Dermatology, vol. 117, no. 6, pp. 1672–1674, 2001.
- R. E. Johnson, C. M. Kondratick, S. Prakash, and L. Prakash, “hRAD30 mutations in the variant form of Xeroderma pigmentosum,” Science, vol. 285, no. 5425, pp. 263–265, 1999.
- B. C. Broughton, A. Cordonnier, W. J. Kleijer et al., “Molecular analysis of mutations in DNA polymerase η in Xeroderma pigmentosum-variant patients,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, no. 2, pp. 815–820, 2002.
- M. Tanioka, T. Masaki, R. Ono et al., “Molecular analysis of DNA polymerase eta gene in Japanese patients diagnosed as Xeroderma pigmentosum variant type,” Journal of Investigative Dermatology, vol. 127, no. 7, pp. 1745–1751, 2007.
- T. Masaki, R. Ono, M. Tanioka et al., “Four types of possible founder mutations are responsible for 87% of Japanese patients with Xeroderma pigmentosum variant type,” Journal of Dermatological Science, vol. 52, no. 2, pp. 144–148, 2008.
- X. Liu, X. Zhang, J. Qiao, and H. Fang, “Identification of a novel nonsense mutation in POLH in a Chinese pedigree with Xeroderma pigmentosum, variant type,” International Journal of Medical Sciences, vol. 10, no. 6, pp. 766–770, 2013.
- O. Messaoud, “Novel mutation in POLH gene responsible of severe phenotype of XP-V,” Clinical Dermatology, vol. 1, pp. 125–129, 2013.
- R. Ono, T. Masaki, S. Takeuchi et al., “Three school-age cases of Xeroderma pigmentosum variant type,” Photodermatology Photoimmunology and Photomedicine, vol. 29, no. 3, pp. 132–139, 2013.
- K. Opletalova, A. Bourillon, W. Yang et al., “Correlation of phenotype/genotype in a cohort of 23 Xeroderma pigmentosum-variant patients reveals 12 new disease-causing POLH mutations,” Human Mutation, vol. 35, no. 1, pp. 117–128, 2014.
- O. Ortega-Recalde, J. I. Vergara, D. J. Fonseca et al., “Whole-exome sequencing enables rapid determination of Xeroderma pigmentosum molecular etiology,” PLoS ONE, vol. 8, no. 6, Article ID e64692, 2013.
- S. A. Miller, D. D. Dykes, and H. F. Polesky, “A simple salting out procedure for extracting DNA from human nucleated cells,” Nucleic Acids Research, vol. 16, no. 3, article 1215, 1988.
- C. Bouchlaka, S. Abdelhak, A. Amouri et al., “Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations,” Journal of Human Genetics, vol. 48, pp. 352–361, 2003.
- N. H. Nicolay, R. Carter, S. B. Hatch et al., “Homologous recombination mediates S-phase-dependent radioresistance in cells deficient in DNA polymerase eta,” Carcinogenesis, vol. 33, no. 11, pp. 2026–2034, 2012.
- Y. W. Chen, J. E. Cleaver, F. Hanaoka, C. F. Chang, and K. M. Chou, “A novel role of DNA polymerase η in modulating cellular sensitivity to chemotherapeutic agents,” Molecular Cancer Research, vol. 4, no. 4, pp. 257–265, 2006.
- D. Gebow, N. Miselis, and H. L. Liber, “Homologous and nonhomologous recombination resulting in deletion: effects of p53 status, microhomology, and repetitive DNA length and orientation,” Molecular and Cellular Biology, vol. 20, no. 11, pp. 4028–4035, 2000.
- P. L. Deininger and M. A. Batzer, “Alu repeats and human disease,” Molecular Genetics and Metabolism, vol. 67, no. 3, pp. 183–193, 1999.