- Research article
- Open Access
A novel point mutation within the EDA gene causes an exon dropping in mature RNA in Holstein Friesian cattle breed affected by X-linked anhidrotic ectodermal dysplasia
BMC Veterinary Researchvolume 7, Article number: 35 (2011)
X-linked anhidrotic ectodermal dysplasia is a disorder characterized by abnormal development of tissues and organs of ectodermal origin caused by mutations in the EDA gene. The bovine EDA gene encodes the ectodysplasin A, a membrane protein expressed in keratinocytes, hair follicles and sweat glands, which is involved in the interactions between cell and cell and/or cell and matrix. Four mutations causing ectodermal dysplasia in cattle have been described so far.
We identified a new single nucleotide polymorphism (SNP) at the 9th base of exon 8 in the EDA gene in two calves of Holstein Friesian cattle breed affected by ectodermal dysplasia. This SNP is located in the exonic splicing enhancer (ESEs) recognized by SRp40 protein. As a consequence, the spliceosome machinery is no longer able to recognize the sequence as exonic and causes exon skipping. The mutation determines the deletion of the entire exon (131 bp) in the RNA processing, causing a severe alteration of the protein structure and thus the disease.
We identified a mutation, never described before, that changes the regulation of alternative splicing in the EDA gene and causes ectodermal dysplasia in cattle. The analysis of the SNP allows the identification of carriers that can transmit the disease to the offspring. This mutation can thus be exploited for a rational and efficient selection of unequivocally healthy cows for breeding.
Ectodermal dysplasia (ED) is a genetic disease characterized by abnormal development of tissues and organs of ectodermal origin, including teeth, hair, nails and sweat glands . There are different forms of ED, the most common of which is caused by mutations in X-linked ectodysplasin gene A (EDA). It has been described in human , mouse , dog  and cattle . Common features shown by the affected individuals are hypodontia, sparse hair and absence of sweat glands.
In cattle, the gene EDA is located on chromosome X q22  and encodes ectodyslpasin-A, a membrane protein expressed in keratinocytes, hair follicles and sweat glands, which is involved in the interaction between cell and cell and/or cell and matrix. The EDA gene may encode for two protein isoforms, EDA1 and EDA2, that differ for the presence or absence of two aminoacids . These two isoforms are members of TFN family.
Since the disease follows X-linked recessive transmission, only males present the full form, while heterozygous females (carriers) are asymptomatic or show slight symptoms, such as hypotrichosis and reduction in the number of teeth. The genetic transmission of this disease in cattle was described by Drögemüller and collaborators , who found a deletion of the whole exon 3 of EDA gene in an affected German Holstein calves and proposed to use for the bovine disease the name of the homologous human syndrome. The same authors subsequently described a G/T mutation at the beginning of intron 8 that leads to a defect in splicing and an in-frame protein deletion of 51 or 45 base pairs with respect to the EDA1 and EDA2 transcripts  and a C/T SNP at position 24 of exon 6 that causes a nonsense mutation of arginine (R) into a stop codon (X) .
Recently a new case of ectodermal dysplasia was reported in Danish Red Holstein cattle by Karlskov-Mortensen and collaborators . They found a new transcript variant including an insertion of 161 bp LINE fragment between exon1 and exon 2.
In our study we screened the EDA gene in two affected calves and some of their close relatives, for a total of eight animals, in order to identify the mutations causing the disease in Holstein Friesian cattle breed.
Cattle samples were screened for mutations through DNA and RNA sequence analysis. By sequencing the DNA of the sampled individuals, we identified a single nucleotide polymorphism (SNP) G/A at the 9th base of exon 8 [GenBank: AJ278907.1 position 30.549]. Both affected calves were hemizygous A/-, the mother and the four sisters were heterozygous G/A (therefore all carriers), the healthy brother was hemizygous G/- (Figure 1,2). To verify if the mutation had effects on exon splicing we performed an analysis using Human Splicing Finder software . The results revealed that the mutation is located within the exonic splicing enhancer (ESE) recognized by SR proteins.
At the RNA level we performed reverse transcriptase PCR (RT-PCR) and sequencing of the cDNA. In the affected calves a deletion in the amplified band of 323 bp, shown by healthy animals (Figure 3), compatible in size with the skipping of the whole exon 8 (131 bp), was observed. The mother and the four sisters presented two bands of 323 bp and 192 bp, corresponding to those of healthy and affected individuals respectively. Sequencing of the RT-PCR products revealed that the amplified fragment of the affected animals lacked exactly 131 bp, corresponding to exon 8. At the protein level, the exon skipping leads to a frameshift and consequently to a premature stop codon. The mutated protein is lacking in 119 amino acids (about half of the protein) including the TFN domain (Figure 4).
The identification of mutations causing a genetic disease is of great economic importance as it allows diagnosing the healthy carriers, and then the eradication of the disease. In this study we identified a new mutation in the bovine EDA gene causing ectodermal dysplasia in Holstein Friesian cattle breed.
The G/A transversion we found in the affected calves causes a change from the glycine residue encoded by the wild type allele to a serine residue. This missense mutation changes both amino acid sequence and protein structure causing deleterious effects. Several studies have shown that some missense mutations, located in exonic splicing regulatory elements, can cause diseases by altering the splicing machinery process . The mutation we identified causes the incorrect splicing of both gene isoforms (EDA1, EDA2). In the mutated individuals the whole exon 8 is excluded from the final mRNA sequence during the splicing process.
The accurate removal of introns from pre-mRNA is essential for correct gene expression. Splicing is primarily regulated by splice-site motifs between intron and exon junctions . In addition to the splice-site motifs, several studies have shown that other sequences are involved in the regulation of splicing process [17–19]. They form two classes of regulatory elements: exonic splicing enhancers (ESEs), recognized by SR proteins, and exonic splicing silencers (ESSs), recognized by hnRNP proteins [18–21]. These sequences have been identified by experimental and computational approaches .
In our study, the analysis of splicing revealed that the mutation is located within the exonic splicing enhancer (ESEs) sequences recognized by SRp40 protein. The function of SR proteins is binding to exonic sequences and enhancing the identification of the flanking splice site .
Several studies have demonstrated that single point mutations in exonic splicing enhancers (ESEs) lead to disease development [24–26]. For example, a C/T mutation in ESE sequence found in the human mitochondrial acetoacetyl-CoA thiolase gene results in exon 10 skipping. The protein is no more functional causing the mitochondrial acetoacetyl-CoA thiolase (T2) deficiency disorder . Two silent substitutions in the Pyruvate dehydrogenase complex (PDHA1 gene) found in most patients with PDHc deficiency cause exon 5 skipping by disruption of a putative exonic splicing enhancer .
The EDA protein consists of a TFN domain for binding to the receptor, a collagen domain and cutting sites for furin. The TNF domain sequence is strongly conserved between cattle, human, mouse and dog demonstrating the presence of a very important motif in this region. The mutation we discovered influences the splicing process leading to the formation of a truncated protein. In the individuals presenting the described G > A transversion, SRp40 protein is no longer able to recognise the ESE sequence resulting in skipping of exon 8 (Figure 5). At the protein level, this leads to a frameshift deletion causing the loss of the TFN domain in the mutated ectodysplasin. The truncated EDA protein is no longer functional thus causing the ectodermal dysplasia disease.
Recently a mutation that leads to a truncated EDA protein was reported in Danish Red Holstein cattle. This mutation is an insertion of a LINE element between exon1 and exon2 in the EDA transcript, causing a frameshift which introduces a premature stop codon in the beginning of exon 2 . Our results are in agreement with the data of Drögemüller et al. , reporting a point mutation within the 5' splice site of intron 8 in cattle EDA gene. The mutated transcript described by those authors uses a cryptic internal splice acceptor site within exon 8. The mutation we identified is located within the same cryptic splice site: this is a further confirmation supporting the involvement of the SNP we described in the splicing process.
We identified a new single nucleotide mutation that causes ectodermal dysplasia in Holstein Friesian cattle breed. The analysis of this SNP allows the identification of the three possible genotypes (healthy, affected and carrier) and thus can be used to highlight carrier cows that can transmit the disease to the offspring. Ectodysplasia causes a significant economic loss: the use of heterozygous carriers in breeding results in a 25% chance of birth of an affected animal and 25% of birth of a carrier. Therefore, the early screening for heterozygotes that are carriers of the described mutation but do not exhibit the disease would particularly useful.
Eight animals (two affected males, their mother, a healthy brother and four sisters), plus one healthy control of Friesian breed, were screened for mutations within the EDA gene. The affected animals showed complete hypodontia and a generalized hypotrichosis with a short hair coat (Figure 6). The severity of hypotrichosis varied in different areas of the body: both animals showed a short hair coat on the head, around eyes and on the tail. Moreover the neck, the flanks and the ventral abdomen appeared completely hairless. The skin was wrinkled especially on the neck. The absence of hair coat caused chronic skin problems such abrasion in both animals. These excoriations were more severe on the back. The mother showed mild symptoms of disease. We observed a partial hypotrichosis and hypodontia. The deficiency of the hair coat was more severe around ears while hair coat was normal on the flanks. Concerning dentition, we found only four incisors instead of eight and all teeth were long and pointed (Figure 7). Molars were normal in number and morphology. Moreover, one female showed an abnormal dentition with a partial hypodontia. We observed only four incisors bad positioned while the hair coat was normal. All other females are phenotypically sane.
Blood samples were collected in EDTA tubes and frozen at -20°C until extraction. Genomic DNA was isolated using DNeasy Blood & Tissue Kit (Qiagen), checked for DNA quality on agarose gel and quantified using a DTX microplate reader (Beckman Coulter) after staining with Picogreen (Invitrogen).
Skin samples were put in RNAlater (Sigma) immediately after collection and stored at -80°C. Total RNA was extracted from skin and blood using RNeasy tissue Kit (Qiagen) and RNeasy blood Kit (Qiagen) respectively and quantified using a DTX microplate reader (Beckman Coulter) using Quant-it RNA assay (Invitrogen).
Blood and skin samples collection were performed according to the Animal Ethics Committee of CRA, Italy, in agreement with local ethical requirements.
Using a forward (5' TGGGGGTTGTGTACAG 3') and a reverse (5' TCAGCCATTGGCTGGTCTGGGC 3') primer located in intron 7 and intron 8 respectively , each PCR reaction was performed in 25 ul containing 10 ng of genomic DNA, 0.2 mM dNTP, 20 pmol of each primer, 1X buffer and 2U Taq polymerase (Bioline). After a 5 min initial denaturation at 94°C, 30 cycles of 30 sec at 94°C, 1 min at 55°C and 1 min at 72°C were carried out. After exosap (USB) purification, the PCR products were sequenced from both directions using the same primers with a CEQ8800 sequencer (Beckman Coulter) using DTCS kit (Beckman Coulter) according to manufacturer's instructions.
RT-PCR one step (Qiagen) was performed on total RNA using a forward primer (5' ATAAAGCTGGAACTCGAG 3') located in exon 6 and a reverse primer (5' TTGCCTGTCTCAATACTG 3') located in exon 9 . The reaction was performed in 25 ul containing 10 ug RNA, 1X Buffer, 0.2 mM dNTP, 0.6 uM of each primer and 1 ul RT-PCR Enzyme (Qiagen). After a 30 min reverse transcription at 50°C and 15 min at 95°C, 30 cycles of 30 sec at 94°C, 1 min at 55°C and 1 min at 72°C were performed.
The RT-PCR products were sequenced from both directions using the same primers as described above.
Sequences analysis and alignment were performed using Bioedit software .
In order to study the effects of mutations on splicing signals we used Human Splicing Finder Version 2.4.1  available at http://www.umd.be/HSF/. The software provides a tool to predict the effects of mutations on splicing signals and to identify splicing motifs in the sequence of interest.
Pinheiro M, Freire Maia: Ectodermal dysplasias: a clinical classification and a causal review. Am J Med Genet. 1994, 53: 153-162. 10.1002/ajmg.1320530207.
Kupietzky A, Houpt M: Hypohidrotic ectodermal dysplasia: characteristics and treatment. Quintessence Int. 1995, 26: 285-291.
Ferguson BM, Brockdorff N, Formstone E, Ngyuen T, Kronmiller JE, Zonana J: Cloning of Tabby, the murine homolog of the human EDA gene: evidence for amembraneassociated protein with a short collagenous domain. Hum Mol Genet. 1997, 6: 1589-1594. 10.1093/hmg/6.9.1589.
Lewis JR, Reiter AM, Mauldin EA, Casal ML: Dental abnormalities associated with X-linked hypohidrotic ectodermal dysplasia in dogs. Orthod Craniofac Res. 2010, 13 (1): 40-7. 10.1111/j.1601-6343.2009.01473.x.
Drögemüller C, Distl O, Leeb T: Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle. Genome Res. 2001, 11 (10): 1699-705. 10.1101/gr.182501.
Tariq M, Wasif N, Ayub M, Ahmad W: A novel 4-bp insertion mutation in EDA1 gene in a Pakistani family with X-linked hypohidrotic ectodermal dysplasia. Eur J Dermatol. 2007, 17 (3): 209-12.
Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Merrer ML, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A: Only four genes (EDA1, EDAR, EDARADD and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases. Hum Mutat. 2010, 32: 70-77.
Tomb R, Soutou B, Zalloua P: Anhidrotic ectodermal dysplasia. Report of a rare mutation in EDA1. Ann Dermatol Venereol. 2009, 136 (1): 28-31. 10.1016/j.annder.2008.04.018.
Srivastava AK, Pispa J, Hartung AJ, Du Y, Ezer S, Jenks T, Shimada T, Pekkanen M, Mikkola ML, Ko MS, Thesleff I, Kere J, Schlessinger D: The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains. Proc Natl Acad Sci USA. 1997, 94 (24): 13069-74. 10.1073/pnas.94.24.13069.
Kuiper H, Kutschke L, Drögemüller C, Leeb T, Distl O: Assignment of the bovine ectodysplasin A gene (ED1) to bovine Xq22- > q24 by fluorescence in situ hybridization. Cytogenet Cell Genet. 2001, 92 (3-4): 356-7. 10.1159/000056932.
Drögemüller C, Peters M, Pohlenz J, Distl O, Leeb T: A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle. J Mol Med. 2002, 80 (5): 319-23. 10.1007/s00109-002-0320-z.
Drögemüller C, Barlund CS, Palmer CW, Leeb T: A novel mutation in the bovine EDA gene causing anhidrotic ectodermal displasia. Arch Tierz Dummerstorf. 2006, 49: 615-616.
Karlskov-Mortensen P, Cirera S, Nielsen L, Arnbjerg J, Reibel J, Fredholm M, Agerholm JS: Exonization of a LINE1 fragment implicated in X-linked hypohidrotic ectodermal dysplasia in cattle. Anim Genet. 2011
Desmet FO, Hamroun D, Lalande M, Collod-Béroud G, Claustres M, Béroud C: Human Splicing Finder: an online bioinformatics tool to predict splicing signals. Nucleic Acids Res. 2009, 37 (9): e67-10.1093/nar/gkp215.
Gorlov IP, Gorlova OY, . Frazier ML, Amos CI: Missense Mutations in hMLH1 and hMSH2 Are Associated with Exonic Splicing Enhancers. Am J Hum Genet. 2003, 73: 1157-1161. 10.1086/378819.
Woolfe A, Mullikin JC, Elnitski L: Genomic features defining exonic variants that modulate splicing. Genome Biol. 2010, 11 (2): R20-10.1186/gb-2010-11-2-r20.
Long JC, Caceres JF: The SR protein family of splicing factors: master regulators of gene expression. Biochem J. 2009, 417 (1): 15-27. 10.1042/BJ20081501.
Cartegni L, Krainer AR: Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1. Nat Genet. 2002, 30 (4): 377-84. 10.1038/ng854.
Black DL: Mechanisms of alternative pre-messenger RNA splicing. Annu Rev Biochem. 2003, 72: 291-336. 10.1146/annurev.biochem.72.121801.161720.
Jensen CJ, Oldfield BJ, Rubio JP: Splicing, cis genetic variation and disease. Biochem Soc Trans. 2009, 37 (6): 1311-5. 10.1042/BST0371311.
Berasain C, Goñi S, Castillo J, Latasa MU, Prieto J, Avila MA: Impairment of pre-mRNA splicing in liver disease: mechanisms and consequences. World J Gastroenterol. 2010, 16 (25): 3091-102. 10.3748/wjg.v16.i25.3091.
Akerman M, David-Eden H, Pinter RY, Mandel-Gutfreund Y: A computational approach for genome-wide mapping of splicing factor binding sites. Genome Biol. 2009, 10 (3): R30-10.1186/gb-2009-10-3-r30.
Lin S, Fu XD: SR proteins and related factors in alternative splicing. Adv Exp Med Biol. 2007, 623: 107-22. 10.1007/978-0-387-77374-2_7.
Fukao T, Horikawa R, Naiki Y, Tanaka T, Takayanagi M, Yamaguchi S, Kondo N: A novel mutation (c.951C > T) in an exonic splicing enhancer results in exon 10 skipping in the human mitochondrial acetoacetyl-CoA thiolase gene. Mol Genet Metab. 2010, 100 (4): 339-44. 10.1016/j.ymgme.2010.03.012.
Boichard A, Venet L, Naas T, Boutron A, Chevret L, de Baulny HO, De Lonlay P, Legrand A, Nordman P, Brivet M: Two silent substitutions in the PDHA1 gene cause exon 5 skipping by disruption of a putative exonic splicing enhancer. Mol Genet Metab. 2008, 93 (3): 323-30. 10.1016/j.ymgme.2007.09.020.
Moseley CT, Mullis PE, Prince MA, Phillips JA: An exon splice enhancer mutation causes autosomal dominant GH deficiency. J Clin Endocrinol Metab. 2002, 87 (2): 847-52. 10.1210/jc.87.2.847.
Hall TA: BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acids Symp Ser. 1999, 41: 95-98.
We want to thank Mrs Gabriella Porcai for technical assistance and Dr. Riccardo Fortunati who kindly provided samples.
MG carried out the molecular genetic studies and drafted the manuscript. AV participated in design and coordination of the study. LP carried out the design of the study and helped to draft the manuscript. All authors read and approved the final manuscript.
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