Transcription start sites and epigenetic analysis of the HSD17B10 proximal promoter
© Yang et al.; licensee BioMed Central Ltd. 2013
Received: 27 March 2013
Accepted: 2 July 2013
Published: 8 July 2013
Hydroxysteroid (17beta) dehydrogenase X (HSD10) is a multifunctional protein encoded by the HSD17B10 gene at Xp11.2. In response to stress or hypoxia-ischemia its levels increase rapidly. Expression of this gene is also elevated significantly in colonic mucosa of the inactive ulcerative colitis patients. However, accurate information about its several transcripts is still lacking, and additional evidence for its escape from X-chromosome inactivation remains to be obtained in order to help settle a debate (He XY, Dobkin C, Yang SY: Does the HSD17B10 gene escape from X-inactivation? Eur J Hum Genet 2011, 19: 123-124).
Two major HSD17B10 transcription start sites were identified by primer extension at -37 and -6 as well as a minor start site at -12 nucleotides from the initiation codon ATG. Epigenetic analysis of the 5’-flanking region of the HSD17B10 gene showed that there was little 5-methylcytosine (<3%) in a normal male, and that none of CpG dinucleotides in the CpG island approached 50% methylation in females.
The actual length of first exon of the HSD17B10 gene was found to be about a quarter larger than that originally reported. Its transcripts result from a slippery transcription complex. The hypomethylation of the CpG island provides additional evidence for the variable escape of the HSD17B10 gene from X-chromosome inactivation which could influence the range of severity of HSD10 deficiency, an inherited error in isoleucine metabolism, in heterozygous females.
KeywordsCpG island DNA methylation TATA-less promoter X-chromosome inactivation HSD10 deficiency
Hydroxysteroid (17beta) dehydrogenase X (HSD10) is encoded by the HSD17B10 gene at Xp11.2 . HSD10 is a multifunctional enzyme involved in the degradation of isoleucine and branched-chain fatty acids, the metabolism of steroid hormones and neuroactive steroids as well as aldehyde detoxification [2, 3]. Furthermore, it complexes with other proteins to generate RNase P activity . Various HSD10 functions are inhibited when it is bound to the amyloid-β peptide  or estrogen receptor alpha .
Mutations in the HSD17B10 gene and its aberrant expression result in HSD10 deficiency (OMIM#300438) [7, 8], X-linked mental retardation, and abnormal behavior (MRXS10) (OMIM#300220) . Accumulation of HSD10 in neurons is also involved in the pathogenesis of Alzheimer disease (AD) . Elevated levels of HSD10 are found in the cerebrospinal fluid (CSF) of patients with AD and multiple sclerosis . HSD10 levels vary significantly among different brain regions and in response to stress and hypo-ischemia [12, 13]. The expression of the HSD17B10 gene was also significantly elevated in colonic mucosa of the inactive ulcerative colitis patients [14, 15]. In order to lay the foundation for designing effective treatment of these disease conditions, it is essential to elucidate the molecular mechanism of the HSD17B10 gene’s expression. For this reason we sought accurate information about its transcripts and DNA methylation of its CpG island.
Here we report that there are several transcription start sites. The predominant transcript, HSD10 variant 1, starts at -37 or -6 nucleotides from the ATG initiation codon. In addition we found that none of CpG dinucleotides in the in the HSD17B10 proximal promoter CpG island region, approached 50% methylation in female genomic DNA. Since X inactivation of HSD17B10 would be expected to result in nearly complete methylation of this region in one of the two copies of this gene, this hypomethylation of the CpG island, together with previously reported data of HSD17B10 expression in somatic cell hybrids , suggests that this gene may have a variable escape from X-chromosome inactivation.
This study was approved by the Institutional Review Board of NYS Institute for Basic Research in Developmental Disabilities. The human DNA samples were obtained in conformance with the Internal Review Board’s guidelines and included the acquisition of written informed consent.
Chromosomal DNA was isolated from blood samples of normal individuals (one male and two females) with the FlexiGene kit (http://www.qiagen.com) and used as the template for the HSD17B10 gene-specific methylation analysis.
Primer extension analysis
Total human brain RNA was purchased from Clontech. A primer HBHADPE3 (5’-CAGGTCCAGAAGCACAGCAGAGGCT-3’) specific to HSD17B10 was synthesized. This primer and phiX174 DNA/Hinf1 marker obtained from Promega were 5’-labeled, respectively, by using [γ-32P]ATP and T4 polynucleotide kinase as previously described . 25μg human brain RNA mixed with 1 pmol of 32P-labeled primer in 17μl of buffer containing 75 mM KOAc, 50 mM Tris-HCL (pH 8.3), 8 mM Mg(OAc)2, and 10 mM DTT was denatured in a heating block set at 100°C for 2 min, and then cooled quickly on ice. This sample was transferred to a 42°C water bath for hybridization for at least 30 min. During the annealing reaction, the sample was mixed with 2 μl dNTP (2mM each of dATP, dGTP, dTTP and 10 μCi [α-32P]dCTP) and 1 μl of AMV reverse transcriptase (20 units). Finally, 2 mM dCTP was added and the extension reaction proceeded at 42°C for another 30 min, as previously described in principle . Three parallel experiments, either without RNA or without primer or without reverse transcriptase, were performed as controls. At the end of the primer extension, 4 μl of 0.5 M EDTA was added to stop the reaction. After the nucleic acid was recovered by ethanol precipitation, the pellet was resuspended in 6 μl of formamide gel loading buffer. Primer extension products were separated by electrophoresis on an 8% polyacrylamide gel in parallel with the [γ-32P]-labeled phiX174 DNA/Hinf1 marker and a dideoxy sequencing ladder from the dideoxy sequencing of a plasmid containing the HSD17B10 5’-flanking region ligated to the same gene's coding sequence.
Methylation assay target sequences
Genomic target sequence
Bisulfite converted target sequence
Pyrosequencing dispensation order
ccacgccccacgtctcatgcggcagcggcagacgccccggcccgtcgatccgccccttccgccgcttcgcctcggccaatcaacgagcgcccgcgcccccatcCCCATCCCGTGGAGTGGCCGGCGACAAGATGG (c>g, polymorphism rs1264014)
Multiple transcription start sites of HSD17B10 gene
Hypomethylation of the CpG island in 5’-fflanking region of the HSD17B10 gene
HSD10 which is encoded by the HSD17B10 gene , has both enzymatic and non-enzymatic functions that are central to a number of developmental disabilities and AD . The HSD17B10 proximal promoter has a CCAAT box (-56/-52 from ATG), but no TATA box (Figure 1B). So far fourteen different types of hydroxysteroid (17β) dehydrogenases have been identified in mammalian cells . Genes encoding different types of hydroxysteroid (17β) except that for the type 1 hydroxysteroid (17β) dehydrogenase (HSD17B1), have a binding site for CCAAT enhancer binding factors (C/EBPs) in their promoters. A study focused on the impact of this family of transcription factors on gene expression in a hepatocarcinoma cell line HepG2 found that both HSD17B8 and HSD17B10 were regulated by C/EBPβ .
Three splice variants of HSD10 have been reported . Since the ratio of HSD10 mRNA isoform 1 versus those of 2 and 3 is 3280:1:52 , the transcription start sites identified in this study are most likely related to the transcript of HSD10 variant 1 and probably to 2 and 3 as well, although this remains to be determined.
It was reported that there is approximately a 5-fold increase of HSD10 antigen in cortical neurons in the region surrounding cerebral ischemia consequent to stroke . This observation suggest that the HSD17B10 may be a hypoxia-responsive gene. Moreover, a significant change of HSD17B10 expression was found in the colonic mucosa of patients with ulcerative colitis [14, 15]. We examined alternative transcription start sites because alternative transcription start site usage has been linked to disease . The first major transcription start site in human brain was identified 37 nucleotides upstream from the ATG initiation codon (see “a” in Figure 1B). This is 6 nucleotides upstream from the start of Ref. Seq NM_004493.2 (Figure 1B), which is itself 6 nucleotides upstream from the start site in the sequence we originally deposited to GenBank (AF035555.1) in 1997. The results indicate that the actual length of first exon of this gene is about one and a quarter of that reported previously . The multiple transcription start sites identified here not only locate the RNA polymerase II binding sites but also suggest that the transcription complex may shift within this promoter.
The HSD17B10 promoter qualifies as a high CpG density (HC) promoter (see Table 1), which is often associated with housekeeping genes . The association between promoter methylation and transcriptional silencing is well established and promoter methylation is a reliable epigenetic mark of XCI . The methylation analysis of a CpG island that overlaps a promoter, along with measurements of the relative expression of each allele identified by SNPs or expression analysis in somatic cell hybrids [16, 28, 29], is one of the most useful methods to predict the genes that escape XCI . The epigenetic analysis of the HSD17B10 proximal promoter showed that it is unmethylated in male DNA (<3% 5-methylcytosine) as expected, but that only about 20% of the cytosines in CpG dinucleotides is methylated in female DNA (Figure 2). Since CpG island-containing promoters are usually highly methylated on the inactive X and unmethylated on the active X, analysis of female DNA usually shows approximately 50% methylation of CpG islands of genes subject to XCI. This is the net result of approximately100% methylation of genes on the inactive X and their complete lack of methylation on the active X. Analysis of male DNA shows only the pattern of the active X—the absence of methylation . Thus the remarkably low methylation level of this HC promoter is consistent with the results from expression of the HSD17B10 gene in hybrids showing escape from XCI [16, 28, 29].
Chromosomal DNA isolated from blood is widely used for the methylation analysis of X-linked promoters as leukocytes are non-dividing cells with a short life span . Since it was reported that at least 88% of human genes do not show tissue-specific XCI , data obtained from blood chromosomal DNA generally represents the XCI status in other tissues. This is true for the gene of interest, because the methylation profile of the HSD17B10 proximal promoter shown in Figure 2 was found to be like that of human dorsolateral prefrontal cortex according to the methylomeDB, a database of DNA methylation profiles of the brain . Hypomethylation of this promoter was found in both blood and brain. Although it was previously reported in a study of fibroblasts [33, 34] that the HSD17B10 gene did not escape XCI, the opposite inference  is implied by the data presented here. Data from epigenetic analysis of the HSD17B10 proximal promoter is consistent with a variable escape of this gene from XCI. This suggests that some bi-allelic expression of this gene may occur in female cells, which could add to the variability in expression imposed by mosaicism of XCI . It is conceivable that the variable escape may allow more cells to have at least some wild type HSD10 in a female carrying a missense mutation on the HSD17B10 gene.
Missense mutations of the HSD17B10 gene result in an X-linked metabolic disease in males while most females are asymptomatic . So far only two female cases with severe developmental disabilities have been reported [37, 38]. More interestingly, female patients uniformly present milder clinical manifestations than male patients carrying the same mutations. The variable escape of the HSD17B10 gene from XCI may provide another protective factor for a female for alleviation of HSD10 deficiency.
The actual length of first exon of the HSD17B10 gene was found to be about a quarter larger than that originally reported. Its transcripts result from a slippery transcription complex. The hypomethylation of the CpG island in the proximal promoter of the HSD17B10 gene provides additional evidence for the variable escape of the HSD17B10 gene from X-chromosome inactivation which could influence the range of severity of HSD10 deficiency, an inherited error in isoleucine metabolism, in heterozygous females.
SYY: MD, PhD, email: email@example.com, Head of the Medical Biochemistry Lab;
CD: PhD, email: Carl.Dobkin@opwdd.ny.gov, Head of the Molecular Genetics Lab;
XYH: PhD, email: firstname.lastname@example.org, Senior Scientist;
WTB: MD, PhD, email@example.com, Director of the NYSIBRDD.
This work was supported by the New York State Office for People with Developmental Disabilities. We thank Dr. M. Junaid for his help in collecting data and two anonymous reviewers for their comments.
- Yang SY, He XY, Miller D: HSD17B10: A gene involved in cognitive function through metabolism of isoleucine and neuroactive steroids. Mol Genet Metab. 2007, 92: 36-42. 10.1016/j.ymgme.2007.06.001.View ArticlePubMed
- He XY, Yang SY: Roles of type 10 17beta-hydroxysteroid dehydrogenase in intracrinology and metabolism of isoleucine and fatty acids. Endoc Metab Immun Dis – Drug, Targets. 2006, 6: 95-102. 10.2174/187153006776056639.View Article
- Yang SY, He XY, Schulz H: Multiple functions of type 10 17beta-hydroxysteroid dehydrogenase. Trends Endocrinol Metab. 2005, 16: 167-175. 10.1016/j.tem.2005.03.006.View ArticlePubMed
- Holzmann J, Frank P, Löffler E, Bennett KL, Gerner C, Rossmanith W: RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme. Cell. 2008, 135: 462-474. 10.1016/j.cell.2008.09.013.View ArticlePubMed
- Oppermann UC, Salim S, Tjernberg LO, Terenius L, Jornvall H: Binding of amyloid β-peptide to mitochondrial hydroxyacyl-CoA dehydrogenase (ERAB): regulation of an SDR enzyme activity with implication for apoptosis in Alzheimer’s disease. FEBS Lett. 1999, 451: 238-242. 10.1016/S0014-5793(99)00586-4.View ArticlePubMed
- Jazbutyte V, Kehl F, Neyses L, Pelzer T: Estrogen receptor alpha interacts with 17beta-hydroxysteroid dehydrogenase type 10 in mitochondria. Biochem Biophys Res Commun. 2009, 384: 450-454. 10.1016/j.bbrc.2009.04.139.View ArticlePubMed
- Yang S-Y, He X-Y, Olpin SE, Sutton VR, McMenamin J, Philipp M, Denman RB, Malik M: Mental retardation linked to mutations in the HSD17B10 gene interefering with neurosteroid and isoleucine metabolism. Proc Natl Acad Sci USA. 2009, 106: 14820-14824. 10.1073/pnas.0902377106.PubMed CentralView ArticlePubMed
- Seaver LH, He XY, Abe K, Cowan T, Enns GM, Sweetman L, Lee S, Malik M, Yang SY: A novel mutation in the HSD17B10 gene of a 10-year-old boy with refractory epilepsy, chreoathetosis and learning disability. PLoS One. 2011, 6: e27348-10.1371/journal.pone.0027348.PubMed CentralView ArticlePubMed
- Lenski C, Kooy RF, Reyniers E, Loessner D, Wanders RJA, Winnepenninckx B, Hellebrand H, Engert S, Schwartz CE, Meindl A, Ramser J: The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior. Am J Hum Genet. 2007, 80: 372-377. 10.1086/511527.PubMed CentralView ArticlePubMed
- Yang SY, He XY: Role of type 10 17 beta-hydroxysteroid dehydrogenase in the pathogenesis of Alzheimer’s disease. Neuropathology and Genetics of Dementia. Edited by: Tolnay M, Probst A. 2001, New York: Kluwer Academic, 101-110.View Article
- Kristofiková Z, Bocková M, Hegnerová K, Bartos A, Klaschka J, Rícný J, Rípová D, Homola J: Enhanced levels of mitochondrial enzyme 17beta-hydroxysteroid dehydrogenase type 10 in patients with Alzheimer disease and multiple sclerosis. Mol Biosyst. 2009, 5: 1174-1179. 10.1039/b904799a.View ArticlePubMed
- He XY, Wegiel J, Yang YZ, Pullarkat R, Schulz H, Yang SY: Type 10 17beta-hydroxysteroid dehydrogenase catalyzing the oxidation of steroid modulators of γ-aminobutyric acid type A receptors. Mol Cell Endocrinol. 2005, 229: 111-117. 10.1016/j.mce.2004.08.011.View ArticlePubMed
- Yan SD, Zhu Y, Stern ED, Hwang YC, Hori O, Ogawa S, Frosch MP, Conolly ES, McTaggert R, Pinsky DJ, Clarke S, Stern DM, Ramasamy R: Amyloid β-peptide-binding alcohol dehydrogenase is a component of the cellular response to nutritional stress. J Biol Chem. 2000, 275: 27100-27109.PubMed
- He XY, Yang YX, Yang SY: Changes of the HSD17B10 gene expression levels in ulcerative colitis. Inflamm Bowel Dis. 2013, 19: E23-E24. 10.1002/ibd.22882.View ArticlePubMed
- De Preter V, Arijs I, Windey K, Vanhove W, Vermeire S, Schuit F, Rutgeerts P, Verbeke K: Impaired butyrate oxidation in ulcerative colitis is due to decreased butyrate uptake and a defect in the oxidation pathway. Inflamm Bowel Dis. 2012, 18: 1127-1136. 10.1002/ibd.21894.View ArticlePubMed
- He XY, Dobkin C, Yang SY: Does the HSD17B10 gene escape from X-inactivation?. Eur J Hum Genet. 2011, 2011 (19): 123-124.View Article
- He XY, Schulz H, Yang SY: A human brain L-3-hydroxyacyl-CoA dehydrogenase is identical with an amyloid β-peptide binding protein involved in Alzheimers disease. J Biol Chem. 1998, 273: 10741-10746. 10.1074/jbc.273.17.10741.View ArticlePubMed
- Chaconas G, van der Sande JH: z-32P labeling of RNA and DNA fragments. Methods Enzymol. 1980, 65: 75-85.View ArticlePubMed
- He Yang XY, Schulz H, Elzinga M, Yang SY: Nucleotide sequence of the promoter and fadB gene of the fadBA operon and primary structure of the multifunctional fatty acid oxidation protein from E. coli. Biochemistry. 1991, 30: 6788-6795. 10.1021/bi00241a023.View Article
- Sheridan SD, Theriault KM, Reis SA, Zhou F, Madison JM, Daheron L, Loring JF, Haggarty SJ: Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragil X syndrome. PLoS One. 2011, 6: e26203-10.1371/journal.pone.0026203.PubMed CentralView ArticlePubMed
- Kavanagh DH, Dwyer S, O’Dovovan MC, Owen MJ: The ENCODE project: implication for psychiatric genetics. Mol Psychiatry. 2013, 18: 540-542. 10.1038/mp.2013.13.View ArticlePubMed
- Yang SY, He XY, Miller D: Hydroxysteroid (17β) dehydrogenase X in human health and disease. Mol Cell Endocrinol. 2011, 343: 1-6. 10.1016/j.mce.2011.06.011.View ArticlePubMed
- Moeller G, Adamski J: Integrated view on 17beta-hydroxysteroid dehydrogenases. Mol Cell Endocrinol. 2009, 301: 7-19. 10.1016/j.mce.2008.10.040.View ArticlePubMed
- Rotenin M, Villar J, Celay J, Encio I: Type 10 17β-hydroxysteroid dehydrogenase expression is regulated by C/EBPβ in HepG2 cells. J Steroid Biochem Mol Biol. 2010, 122: 164-171. 10.1016/j.jsbmb.2010.07.003.View Article
- Thorsen K, Schepeler T, Oster B, Rasmussen MH, Vang S, Wang K, Hansen KQ, Lamy P, Pedersen JS, Eller A, Mansilla F, Laurila K, Wiuf C, Laurberg S, Dyrskjøt L, Ørntoft TF, Andersen CL: Tumor-specific usage of alternative transcription start sites in colorectal cancer identified by genome-wide exon array analysis. BMC Genomics. 2011, 12: 505-10.1186/1471-2164-12-505.PubMed CentralView ArticlePubMed
- Weber M, Hellmann I, Stadler MB, Ramos L, Paabo S, Rebhan M, Schübeler D: Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nature Genet. 2007, 39: 457-466. 10.1038/ng1990.View ArticlePubMed
- Cotton AM, Lam L, Affleck JG, Wilson IM, Penaherrera MS, McFadden DE, Kobor MS, Lam WL, Robinson WP, Brown CJ: Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation. Hum Genet. 2011, 130: 187-201. 10.1007/s00439-011-1007-8.PubMed CentralView ArticlePubMed
- Miller AP, Willard HF: Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p. 11.22 that escapes X inactivation. Proc Natl Acad Sci USA. 1998, 95: 8709-8714. 10.1073/pnas.95.15.8709.PubMed CentralView ArticlePubMed
- Carrel L, Willard HF: X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature. 2005, 434: 400-404. 10.1038/nature03479.View ArticlePubMed
- Sharp AJ, Stathaki E, Migiavacca E, Brahmachary M, Montgomery SB: DNA methylation profiles of human active and inactive X chromosomes. Genome Res. 2011, 21: 1592-1600. 10.1101/gr.112680.110.PubMed CentralView ArticlePubMed
- Yasukochi Y, Maruyama O, Mahaian MC, Padden C, Euskirchen GM: X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophis. Proc Natl Acad Sci USA. 2010, 107: 3704-3709. 10.1073/pnas.0914812107.PubMed CentralView ArticlePubMed
- Xin Y, Chanrion B, O’Donnell AH, Milekic M, Costa R, Ge Y, Haghighi FG: MethylomeDB: a database of DNA methylation profiles of the brain. Nucleic Acids Res. 2012, 40: D1245-D1249. 10.1093/nar/gkr1193.PubMed CentralView ArticlePubMed
- Garciar-Villoria J, Gort L, Madrigal I, Fons C, Fernandez C, Navarro-Sastre A, Milà M, Briones P, García-Cazorla A, Campistol J, Ribes A: X-inactivation of HSD17B10 revealed by cDNA analysis in two female patients with 17β-hydroxysteroid dehydrogenase 10 deficiency. Eur J Hum Genet. 2010, 18: 1353-1356. 10.1038/ejhg.2010.118.View Article
- Garciar-Villoria J, Gort L, Madrigal I, Fons C, Fernandez C, Navarro-Sastre A, Milà M, Briones P, García-Cazorla A, Campistol J, Ribes A: Reply to He et al. Eur J Hum Genet. 2011, 19: 124-10.1038/ejhg.2010.194.View Article
- Berletch JB, Yang F, Xu J, Carrel L, Disteche CM: Genes that escape from X inactivation. Hum Genet. 2011, 130: 237-245. 10.1007/s00439-011-1011-z.PubMed CentralView ArticlePubMed
- Yang SY, Dobkin C, He XY, Phillip M, Brown WT: A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutation. Gene. 2013, 515: 380-384. 10.1016/j.gene.2012.12.064.View ArticlePubMed
- Ensenauer R, Niederhoff H, Ruiter JP, Wanders RJ, Schwab KO, Brandis M, Lehnert W: Clinical variability in 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency. Ann Neurol. 2002, 51: 656-659. 10.1002/ana.10169.View ArticlePubMed
- Garciar-Villoria J, Navarro-Sastre A, Fons C, Pérez-Cerdá C, Baldellou A, Fuentes-Castelló MA, González I, Hernández-Gonzalez A, Fernández C, Campistol J, Delpiccolo C, Cortés N, Messeguer A, Briones P, Ribes A: Study of patients and carriers with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: difficulties in the diagnosis. Clin Biochem. 2009, 42: 27-33. 10.1016/j.clinbiochem.2008.10.006.View Article
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