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Mutation analysis of Chinese sporadic congenital sideroblastic anemia by targeted capture sequencing
© An et al.; licensee BioMed Central. 2015
Received: 21 February 2015
Accepted: 11 May 2015
Published: 20 May 2015
Congenital sideroblastic anemias (CSAs) comprise a group of heterogenous genetic diseases that are caused by the mutation of various genes involved in heme biosynthesis, iron-sulfur cluster biogenesis, or mitochondrial solute transport or metabolism. However, approximately 40 % of patients with CSA have not been found to have pathogenic gene mutations. In this study, we systematically analyzed the mutation profile in 10 Chinese patients with sporadic CSA.
We performed targeted deep sequencing analysis in ten patients with CSA using a panel of 417 genes that included known CSA-related genes. Mitochondrial genomes were analyzed using next-generation sequencing with a mitochondria enrichment kit and the HiSeq2000 sequencing platform. The results were confirmed by Sanger sequencing. The ALAS2 mutation was detected in one patient. SLC25A38 mutations were detected in three patients, including three novel mutations. Mitochondrial DNA deletions were detected in two patients. No disease-causing mutations were detected in four patients.
To our knowledge, the pyridoxine-effective mutation C471Y of ALAS2, the compound heterozygous mutation W87X, I143Pfs146X, and the homozygous mutation R134C of SLC25A38 were found for the first time. Our findings add to the number of reported cases of this rare disease and to the CSA pathogenic mutation database. Our findings expand the phenotypic profile of mitochondrial DNA deletion mutations. This work also demonstrates the application of a congenital blood disease assay and targeted capture sequencing for the genetic screening analysis and diagnosis of heterogenous genetic CSA.
Sideroblastic anemias comprise a group of disorders that share several characteristics including mitochondrial iron accumulation in bone marrow erythroid precursors (ringed sideroblasts), ineffective erythropoiesis, increased levels of tissue iron, and varying proportions of hypochromic erythrocytes in the peripheral blood [1, 2]. Congenital sideroblastic anemias (CSAs) are rare diseases that are typically characterized by germline genetic mutations that cause defects in mitochondrial heme synthesis, iron-sulfur cluster metabolism, or protein synthesis [1, 2]. Recently, SF3B1 mutations were found in 70 % of patients with myelodysplastic syndrome with ringed sideroblast but were not detected in patients with CSA [3, 4]. The most common CSA is X-linked sideroblastic anemia (XLSA); this CSA is caused by mutations in ALAS2, which encodes 5-aminolevulinate synthase [2, 5]. Mutations in the erythroid-specific mitochondrial transporter SLC25A38 are the most common cause of autosomal recessive CSA [5, 6]. Other known etiologies include mutations in the genes for SLC19A2, GLRX5, PUS1, ABCB7, YARS2, and mitochondrial DNA deletions [5, 7–13]. However, approximately 40 % of CSAs, either alone or accompanied by a syndrome, have no known pathogenic gene mutations [5, 14]. Here, we used a congenital blood disease assay and targeted capture sequencing to genetically screen 10 Chinese patients with sporadic CSA.
Patients and methods
The study protocol was approved by the Institutional Review Boards of the Hematology and Blood Diseases Hospital, CAMS/PUMC (Ethics No. KT2013004-EC-1). Informed consent was obtained from the guardians of the patients following institutional guidelines. We collected ten patients with CSA according to the diagnostic criteria referred to in previous reports . Total DNA was extracted from the bone marrow or peripheral blood leukocytes and oral epithelial cells of the patients and from peripheral blood leukocytes of the available family members using standard methods. We designed a targeted capture sequencing assay to test a panel of 417 blood disease genes, including the seven known CSA-related genes. The targeted genes were enriched using a biotinylated capture probe (MyGenostics, Baltimore, MD, USA) as described previously . Sanger sequencing was used to confirm the mutations. Mitochondrial genome capture sequencing was performed using a mitochondria enrichment kit (MitoCap™, MyGenostics, Beijing, China) as described previously . The enrichment libraries were sequenced using an Illumina HiSeq 2000 sequencer. The 417 genes in the panel that was used for targeted capture sequencing are listed in Additional file 1: Table S1. The primers used for Sanger sequencing are listed in Additional file 2: Table S2. Detailed experimental methods are described in Additional file 3: Figure S1.
Clinical and laboratory features of ten patients with CSA and results of mutation analyses
Response to PPL
MtDNA 6250–12,498 del
Normal HGB at 11-month-old
Died at 7-month-old
ALAS2 c.1412G > A
Normal HGB after PPL treatment
SLC25A38 c.400C > T
SLC25A38 c.560G > A
Loss to follow-up
SLC25A38 c.260G > A,c.429delT,c.431 T > G
A list of mitochondrial genes involving shared deletion fragments
ATP6 (partly delete)
ND5 (partly delete)
Patient no. 3 exhibited typically microcytic-hypochromic anemia and responded well to pyridoxine treatment. Patients with mutations in SLC25A38 had severe microcytic-hypochromic anemia and systemic iron overload very early in life. The two patients with mitochondrial DNA deletions had severe macrocytic anemia at birth that was accompanied by various degrees of neutropenia and thrombocytopenia and exhibited different degrees of dysplasia in bone marrow cell morphology; in particular, vacuoles were present in myeloid and erythroid precursors. These patients developed severe iron overload shortly after birth. Additionally, Patient no. 1 exhibited congenital insulin-dependent diabetes mellitus. At the end of follow-up, the hemoglobin level of Patient no. 1 (11 months old) gradually increased to normal levels since the age of 6 months, and the Patient no. 2 died at the age of 7 months. The clinical features of the patients are listed in Table 1.
Patients without disease-causing mutations presented severe microcytic anemia and were dependent on transfusions since infancy or childhood. Additionally, the bone marrow histopathology and immunohistochemistry of Patient no. 8 exhibited abnormal lymphocyte infiltration, including 35 % of PAX5+, CD79a+, CD20+ B lymphocytes 10 % of CD10+, TdT+ B lymphocytes, and a small number of CD5 + T cells; the positive rate of Ki67 was 70 %, and Bcl-2 was negative. This phenotype was uncommon in previous reports. The ratio of lymphocytes in peripheral blood was normal. In addition, Patient no. 8 exhibited decreased levels of immunoglobulins (IgG 5.75 g/L [7.51–15.6], IgA 0.47 g/L [0.82–4.53], C3 0.67 g/L [0.79–1.52]). Immune fixation electrophoresis demonstrated the absence of monoclonal immunoglobulins and light chains. The patient did not respond to pyridoxine. Recently, mutations in TRNT1 were detected in patients with syndromic CSA that was associated with B cell immunodeficiency, periodic fevers, and developmental delay (SIFD) [17, 18]. However, the patient in our study did not exhibit signs of immunodeficiency or developmental delay. Although two heterozygous frameshift mutations (c.1997_1998insTAAT, c.2155_2156insTATAAGAGATTTCTAA) in the same allele of TRNT1 were detected in Patient no. 8 by Sanger sequencing, the same mutations were detected in the father of Patient No. 8 thus leading us to speculate that these mutations represented a low frequency of polymorphisms. The major clinical features of these patients are listed in Table 1.
The ALAS2 gene is located on Xp11.21 and catalyzes the first and rate-limiting step in the heme biosynthetic pathway in erythroid cells. All of the disease-causing mutations affect the catalytic domain of ALAS2 (encoded by exons 5 to 11) or the enhancer region in intron 1 [5, 14, 19]. Typically, patients with XLSA that is related to the ALAS2 mutation responded to pyridoxine. The novel mutation ALAS2 C471Y observed here further expands the profile of pyridoxine-effective mutations that are recognized to cause XLSA. The mutated amino acid may be located in the middle of a highly conserved hydrophobic region of ALAS2, and its side chain may help to stabilize the PLP-binding site. Therefore, patients with this mutation may respond well to pyridoxine [20, 21].
Patients with CSA caused by SLC25A38 mutation commonly exhibit early onset, no gender differences, severe microcytic-hypochromic anemia, and are nonsyndromic [5, 6]. SLC25A38 might participate in the glycine transport within the mitochondrial membrane and/or the mutual transport of glycine with 5-aminolevulinic acid (ALA) through the mitochondrial membrane (promoting ALA synthesis). The homozygous mutations R134C and R187Q found here are consistent with previous findings of R134H and R187P/Q mutations . R187 residue is the conserved arginine of the arginine-aspartate (RD) dipeptide of transmembrane helix 4, which is thought to provide contact points that determine substrate specificity . In addition, R134 is close to R187 in the three-dimensional structure and is conserved among multiple species. The compound heterozygote mutations that were seen in Patient No. 6 cause protein truncation in both alleles and completely destroy the function of the protein completely and might have caused his far more serious anemia. The potential model of three-dimensional structures of human ALAS2 and its evolutionary conservation of the residues with missense mutations are showed in Additional file 5: Figure S3.
PMPS is associated with large-scale mitochondrial DNA (mtDNA) deletions, rearrangements, or duplications. Typical clinical manifestations include macrocytic anemia and symptoms of mitochondrial diseases with vacuolization of erythroid and myeloid precursors and ring sideroblasts . The patients in our study exhibited typical hematological features but no symptoms of mitochondrial diseases. The deletion fragments were commonly in the sequence range 6250–12,498. The genes involved are listed in Table 2. Among these genes, the COX3 gene product participates in iron ion oxidoreduction reactions as one of the cytochrome C oxidase subunits. Mutations in COX I (also a subunit of cytochrome C oxidase) have been confirmed in patients with acquired idiopathic sideroblastic anemia . Therefore, we speculated that deletion of the COX3 gene might affect the mitochondrial metabolism of iron in the same way. Mitochondrial tRNA participates in the synthesis of all 13 subgroups of enzymes involved in the oxidative phosphorylation of the respiratory chain. Among these proteins, the TRNG tRNA-Gly protein plays a role in mitochondrial glycine transport. Therefore, the deletion of this fragment might affect mitochondrial heme synthesis. ND3, ND4L, ND4, and ND5 are components of NADH dehydrogenase, which is the core element of iron-sulfur clusters. A lack of this enzyme might affect mitochondrial iron metabolism [24, 25]. In conclusion, deletions of mitochondrial genes might reduce heme synthesis and cause iron accumulation in the mitochondria by affecting the transport of cytochrome oxidase C, iron-sulfur clusters, and the substrate.
In this study, we used targeted capture sequencing to detect etiologic mutations in a heterogeneous genetic disease. A novel pyridoxine-effective mutation of ALAS2 and a novel compound heterozygous mutation of SLC25A38 were identified. In addition, we identified fragmental deletions of MtDNA in two patients with CSA using mitochondrial genome capture sequencing, which provided clues for further research on iron metabolism. The utility of targeted capturing sequencing is clear for practical clinical use, especially for heterogenous genetic diseases.
We are grateful to the patients and their family members for participating in this study. This work was funded by the National Natural Science Foundation of China (No. 81270651) and by the Ministry of Education (No. 20121106110036).
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