<abstract xmlns="http://www.w3.org/1999/xhtml"><p>Barth syndrome (BTHS) is a rare X-linked disease characterized by dilated cardiomyopathy, proximal skeletal myopathy and cyclic neutropenia. It is caused by various mutations in the tafazzin (<italic>TAZ</italic>) gene located on Xq28 that results in remodeling of cardiolipin and abnormalities in mitochondria stability and energy production. Here we report on a novel c.285-1G>C splice site mutation in intron 3 of the <italic>TAZ</italic> gene that was detected prenatally.</p></abstract>

Barth syndrome (BTHS) is a rare X-linked disease characterized by dilated cardiomyopathy, proximal skeletal myopathy and cyclic neutropenia. It is caused by various mutations in the tafazzin (TAZ) gene located on Xq28 that results in remodeling of cardiolipin and abnormalities in mitochondria stability and energy production. Here we report on a novel c.285-1G>C splice site mutation in intron 3 of the TAZ gene that was detected prenatally.


<div xmlns="http://www.w3.org/1999/xhtml"><sec id="j_bjmg-2016-0043_s_001_w2aab3b8c44b1b7b1ab1aAa"><div>Introduction</div><p>Barth syndrome (BTHS, OMIM 302060) is a rare X-linked disease characterized by dilated cardiomyopathy, proximal skeletal myopathy and cyclic neutropenia and was first described in 1983 by Barth <italic>et al</italic>. [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_001_w2aab3b8c44b1b7b1ab2b1b1Aa">1</a>]. The incidence of BTHS is about 1 in 300,000-400,000 births [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_002_w2aab3b8c44b1b7b1ab2b1b2Aa">2</a>]. It is also presented with organic aciduria, particularly excess of 3-methylglutaconic acid [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_001_w2aab3b8c44b1b7b1ab2b1b1Aa">1</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_003_w2aab3b8c44b1b7b1ab2b1b3Aa">3</a>]. The excretion of 3-methylglutaconic acid in urine can be highly variable and is often intermittent. At the moment, 3-methylglutaconic acid is a biochemical marker for mitochondrial dysfunction of still unknown origin [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_004_w2aab3b8c44b1b7b1ab2b1b4Aa">4</a>]. Less common features of the disease include hypertrophic cardiomyopathy, isolated left ventricular noncompaction, ventricular arrhythmia, motor delay, poor appetite, fatigue and exercise intolerance, hypoglycemia, lactic acidosis, hyperammonemia and growth delay [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_005_w2aab3b8c44b1b7b1ab2b1b5Aa">5</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_006_w2aab3b8c44b1b7b1ab2b1b6Aa">6</a>]. The main cause of death in infants with BTHS is either heart failure or sepsis due to neutropenia [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_001_w2aab3b8c44b1b7b1ab2b1b1Aa">1</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_002_w2aab3b8c44b1b7b1ab2b1b2Aa">2</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_005_w2aab3b8c44b1b7b1ab2b1b5Aa">5</a>].</p><p>Barth syndrome is caused by various mutations in the <italic>tafazzin</italic> ( <italic>TAZ</italic>, previously termed <italic>G4.5</italic>) gene [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_007_w2aab3b8c44b1b7b1ab2b1b7Aa">7</a>], comprising 11 exons and located on Xq28 [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_008_w2aab3b8c44b1b7b1ab2b1b8Aa">8</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_009_w2aab3b8c44b1b7b1ab2b1b9Aa">9</a>]. This gene encodes a protein tafazzin that plays an important role in remodelling of cardiolipin and phosphatidylglycerol structure [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_001_w2aab3b8c44b1b7b1ab2b1b1Aa">1</a>]. Cardiolipin is a component of the inner mitochondrial membrane. It stabilizes highly ordered respiratory chain supercomplexes and optimises energy production in mitochondria [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_010_w2aab3b8c44b1b7b1ab2b1c10Aa">10</a>]. Studies carried out on a BTHS zebrafish model suggest that the expression of tafazzins is both tissue-specific and age-dependent, and plays an essential role in cardiac development and function [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_011_w2aab3b8c44b1b7b1ab2b1c11Aa">11</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_012_w2aab3b8c44b1b7b1ab2b1c12Aa">12</a>]. We report a novel splice site mutation in intron 3 of the <italic>TAZ</italic> gene in this study.</p></sec><sec id="j_bjmg-2016-0043_s_002_w2aab3b8c44b1b7b1ab1b1Aa"><div>Case Report</div><p>The proband, a 22-year-old primigravida, was referred to the Center for Medical Genetics, Vilnius University Hospital Santariškių Klinikos, Vilnius, Lithuania, at 13 weeks of gestation for genetic counseling because of a familial history of cardiomyopathy. She had three biological brothers. The first brother was healthy. The second brother was born after an uncomplicated pregnancy; on the 9th day after birth, the boy became febrile and was referred to the intensive care unit because of impaired cardiac function, where he was diagnosed with endocardial fibroelas-tosis. Later, the diagnosis was changed to myocarditis. At 4 months of age the boy repeatedly showed symptoms of fever and worsened symptoms of myocarditis. He subsequently died due to cardiac failure at 6 months of age.</p><p>The third brother of the proband was also born after a normal pregnancy and was diagnosed with cardiac insufficiency due to endocardial fibroelastosis on the 3rd week of life after the episode of fever and cyanosis. Since the heart function was improving significantly, the diagnosis was changed to myocarditis. He then developed dilated cardio-myopathy at 5 months of age. Subsequently, at 1 year and 4 months of age the boy presented with an episode of impaired consciousness and convulsion. At that time the boy was diagnosed with hypoglycemia, cardiac insufficiency, repeated episodes of neutropenia, growth retardation and hypotonia. Congenital metabolic disorder was suspected. Biochemical findings included excess amounts of 3-meth-ylglutaric and 3-methylglutaconic acids in urine and low free carnitine in blood. As a result, based on clinical, biochemical findings and family history, BTHS was diagnosed. Genetic testing was not performed at that time. The boy died at 11 years of age of cardiopulmonary insufficiency due to severe pulmonary infection.</p><p>The first trimester ultrasound performed on our proband demonstrated the male sex of the fetus and revealed no markers of chromosomal abnormalities and no fetal pathology. Chorionic villus sampling was performed and molecular tests were carried out. There were no aneuploidies detected and sex chromosomes were XY.</p><p>As the clinical diagnosis of BTHS was defined for our proband’s third brother and the family history highly suggested an X-linked disorder, genetic analysis was performed on the proband’s fetus. Genetic tests were initiated in this order because the purpose of genetic counseling was to investigate if the proband’s fetus had BTHS. Furthermore, as mentioned previously, the third brother of our proband died 10 years ago and it was not possible to start genetic testing on the deceased patient. Informed consent was obtained from all family members who participated in the molecular analyses study.</p></sec><sec id="j_bjmg-2016-0043_s_003_w2aab3b8c44b1b7b1ab1b2Aa"><div>Materials and Methods</div><p>A detailed genealogy of the family was constructed. Inheritance in the presented pedigree was consistent with an X-linked recessive pattern (<a ref-type="fig" href="#j_bjmg-2016-0043_fig_001_w2aab3b8c44b1b7b1ab1b2b2aAa">Figure 1</a>). The DNA of the proband’s fetus (V:1) was extracted from chorionic villi using the InstaGene™ Matrix (Bio-Rad Laboratories, Hercules, CA, USA). The DNA of the proband’s sibling (IV: 12) was extracted from a dried blood spot sample (Guthrie card; Newborn Bloodspot Screening, Wales, Cardiff, UK; <ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://www.newbornbloodspotscreening.wales.nhs.uk/">http://www.newbornbloodspotscreening.wales.nhs.uk/</ext-link>) using the InstaGene™ Matrix (Bio-Rad Laboratories). The DNA of other family members (IV:13, III:8, II:1) was isolated from the venous peripheral blood samples using the phenol-chloroform extraction method. Amplification using specific primers for X-linked <italic>TAZ</italic> gene (NM_ 000116) was performed for the proband’s fetus (V:1). Polymerase chain reaction (PCR) primers for exons 1-11 exons and adjacent intronic regions of the <italic>TAZ</italic> gene were designed using the Primer3 (<ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://bioinfo.ut.ee/primer3-0.4.0/primer3/">http://bioinfo.ut.ee/primer3-0.4.0/primer3/</ext-link>) program [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_013_w2aab3b8c44b1b7b1ab2b1c13Aa">13</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_014_w2aab3b8c44b1b7b1ab2b1c14Aa">14</a>]. Primer sequences are available from the authors upon request. Family members were tested only for the mutation that was observed in the fetus (<italic>i.e</italic>., c.285-1G>C). Amplification products were electrophoresed with TBE 2.0% agarose gel and sequenced using a BigDye Terminator version 3.1 cycle sequence kit (Applied Biosystems, Waltham, MA, USA) on an ABI PRISM™ 3130<italic>xl</italic> sequencer.</p><p><figure id="j_bjmg-2016-0043_fig_001_w2aab3b8c44b1b7b1ab1b2b2aAa" position="float" fig-type="figure"><h2></h2><figCaption><p>Pedigree of the studied family</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_bjmg-2016-0043_fig_001.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/647107522b88470fbea14460/j_bjmg-2016-0043_fig_001.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240717T105543Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240717%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=2a5cdcb3ea54b403fc4d2b8400ab860d56b9b53afec14475ecee491418b72c00" class="mw-100"/></figure></p><sec id="j_bjmg-2016-0043_s_003_s_001_w2aab3b8c44b1b7b1ab1b2b3Aa"><div>Results of Mutational Analyses</div><p>Sequence analysis of the <italic>TAZ</italic> gene identified a hemizygous c.285-1G>C substitution (c.[285-1G>C];[0]) in intron 3 in chorionic villi DNA of the proband’s fetus (V:1). The same hemizygous c.285-1G>C mutation was subsequently identified in the deceased sibling of the proband (IV:12). The mutation was detected in proband’s DNA (IV:13) in the heterozygous form (c.[285-1G>C];[=]) and the carrier status was confirmed. The mother (III:8) and maternal grandmother (II:1) of the proband also carries the mutation (heterozygous genotype for this mutation) [<a ref-type="fig" href="#j_bjmg-2016-0043_fig_002_w2aab3b8c44b1b7b1ab1b2b3b2aAa">Figure 2</a>].</p><p><figure id="j_bjmg-2016-0043_fig_002_w2aab3b8c44b1b7b1ab1b2b3b2aAa" position="float" fig-type="figure"><h2></h2><figCaption><p>The <italic>TAZ</italic> sequencing electrophoregrams showing position c.285-1 of the <italic>TAZ</italic> sequence (NM_000116) (indicated by an arrow).</p><p>(A) The results in the fetus and proband’s sibling: hemizygous mutation (c.[285-1G>C];[0]); A1: forward strand; A2: reverse strand.</p><p>(B) The fragments of the <italic>TAZ</italic> gene sequences of the proband, mother and maternal grandmother: heterozygous form (c.[285-1G>C];[=]); B1: forward strand; B2: reverse strand.</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_bjmg-2016-0043_fig_002.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/647107522b88470fbea14460/j_bjmg-2016-0043_fig_002.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240717T105543Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240717%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=5c9f017dbf26bba2d5420b1051de98f9c15387eddeb1187d0f1c42d2944e4683" class="mw-100"/></figure></p></sec></sec><sec id="j_bjmg-2016-0043_s_004_w2aab3b8c44b1b7b1ab1b3Aa"><div>Discussion</div><p>To date, more than 220 different <italic>TAZ</italic> gene mutations in all exons have been identified [Human Tafazzin (<italic>TAZ</italic> ) Gene Mutation and Variation Database (last updated March 28, 2015; <ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://www.barthsyndrome.org/home">http://www.barthsyndrome.org/home</ext-link>)], 94 of which were found in patients with diagnosed BTHS (Human Gene Mutation Database Professional 2015.4; <ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://www.hgmd.cf.ac.uk/ac/index.php">http://www.hgmd.cf.ac.uk/ac/index.php</ext-link>). Only 13.0% of boys with BTHS carry <italic>de novo</italic> mutations [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_015_w2aab3b8c44b1b7b1ab2b1c15Aa">15</a>]. Phenotype-genotype correlations have not yet been identified [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_016_w2aab3b8c44b1b7b1ab2b1c16Aa">16</a>,<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_017_w2aab3b8c44b1b7b1ab2b1c17Aa">17</a>]. It has been observed that mutations in the <italic>TAZ</italic> gene also result in non syndromic left ventricular non compaction, endocardial fibroelastosis, X-linked infantile cardiomyopathy and dilated cardiomyopathy. Thus, mutations in the <italic>TAZ</italic> gene can result in a broad spectrum of clinical phenotypes including, but not limited to classical BTHS.</p><p>The c.285-1G>C mutation has not been previously reported in the Human Tafazzin (<italic>TAZ</italic>) Gene Mutation and Variation Database (last updated March 28, 2015; <ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://www.barthsyndrome.org/home">http://www.barth syndrome.org/home</ext-link>). The mutation is predicted to alter the wild type constitutive acceptor splice site. Most probably the presence of mutation affects splicing in tafazzin [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_018_w2aab3b8c44b1b7b1ab2b1c18Aa">18</a>]. Family studies showed that the proband, her mother and maternal grandmother carried the same mutation. Our proband’s fetus as well as her brother was affected with BTHS, suggesting that this newly discovered splice site mutation is an anomaly strongly affecting the normal function of the tafazzin protein, and thus, is likely to be pathogenic (<a ref-type="fig" href="#j_bjmg-2016-0043_fig_003_w2aab3b8c44b1b7b1ab1b3b3aAa">Figure 3</a>). An intronic <italic>TAZ</italic> gene mutation (aberrant splicing and elongation of exon 3 because of the insertion of 106 bases between exons 3 and 4) has been reported in a Japanese patient with BTHS, who had very similar symptoms and course of the disease as the third brother of our patient [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_019_w2aab3b8c44b1b7b1ab2b1c19Aa">19</a>]. Our proband decided to terminate the pregnancy. Fetal autopsy was inconclusive.</p><p><figure id="j_bjmg-2016-0043_fig_003_w2aab3b8c44b1b7b1ab1b3b3aAa" position="float" fig-type="figure"><h2></h2><figCaption><p>The location of the c.285-1G>C mutation of the <italic>TAZ</italic> gene and its effect on splicing.</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_bjmg-2016-0043_fig_003.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/647107522b88470fbea14460/j_bjmg-2016-0043_fig_003.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240717T105543Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240717%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=da967245127ca5215c34305a97e6518465dff7987f3854e74219c577bd19c4a9" class="mw-100"/></figure></p><p>Evidence is accumulating that the disorder is substantially underdiagnosed. Historically regarded as a cardiac disease, BTHS is now considered a multi-system disorder that may be first seen by many different specialists. Phenotypic variability raises a major challenge, as some children with BTHS have never showed neutropenia, others lack increased 3-methylglutaconic acid and a minority has occult or absent cardiomyopathy [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_020_w2aab3b8c44b1b7b1ab2b1c20Aa">20</a>]. Furthermore, BTHS was described in 2010 as an unrecognized cause of fetal death. It is recommended that investigation for BTHS should now be seriously considered in male neonates, babies and young boys presenting with idiopathic dilated cardiomyopathy or left ventricular non compaction, and in males with unexplained ventricular arrhythmia or sudden death [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_020_w2aab3b8c44b1b7b1ab2b1c20Aa">20</a>].</p><p>Female carriers are usually healthy and have no cardiovascular pathology. It is however theoretically possible for a female to develop symptoms of the disease because of impaired X chromosome inactivation. The only female ever described with the disease had abnormalities of both X chromosomes [<a ref-type="bibr" href="#j_bjmg-2016-0043_ref_021_w2aab3b8c44b1b7b1ab2b1c21Aa">21</a>]. In this case, the proband, her mother and maternal grandmother had normal electrocardiograms and no history of cardiac disease.</p></sec><sec id="j_bjmg-2016-0043_s_005_w2aab3b8c44b1b7b1ab1b4Aa"><div>Conclusions</div><p>A novel mutation in the <italic>TAZ</italic> gene was identified prenatally in a family with a clinical diagnosis of BTHS. The diagnosis for the proband’s third brother was confirmed by molecular genetic testing and the second brother’s underlying cause of early death was revealed. Mutational analysis offers the possibility of prenatal genetic counseling and preimplantation genetic diagnosis for the family.</p></sec></div>

A novel intronic splice site <italic>tafazzin</italic> gene mutation detected prenatally in a family with Barth syndrome

Vilnius University Hospital Santariškių Klinikos

Balkan Journal of Medical Genetics

This article is distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

A novel intronic splice site  gene mutation detected prenatally in a family with Barth syndrome

Barth syndrome (BTHS) is a rare X-linked disease characterized by dilated cardiomyopathy, proximal skeletal myopathy and cyclic neutropenia. It is caused by...

A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome

Article Category: Case Report

Online veröffentlicht: 31. Dez. 2016

Seitenbereich: 95 - 100

DOI: https://doi.org/10.1515/bjmg-2016-0043

Schlüsselwörter
Barth Syndrome (BTHS), cardiomyopathy, Neutropenia, 3-Methylglutaconin aciduria, () gene

© 2016 Bakšienė M, Benušienė E, Morkūnienė A, Ambrozaitytė L, Utkus A, Kučinskas V

This article is distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome

Article Category: Case Report

Online veröffentlicht: 31. Dez. 2016

Seitenbereich: 95 - 100

DOI: https://doi.org/10.1515/bjmg-2016-0043

SchlüsselwörterBarth Syndrome (BTHS), cardiomyopathy, Neutropenia, 3-Methylglutaconin aciduria, () gene

© 2016 Bakšienė M, Benušienė E, Morkūnienė A, Ambrozaitytė L, Utkus A, Kučinskas V

This article is distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Schlüsselwörter
Barth Syndrome (BTHS), cardiomyopathy, Neutropenia, 3-Methylglutaconin aciduria, () gene