- Open Access
Unraveling the disease pathogenesis behind lethal hydrolethalus syndrome revealed multiple changes in molecular and cellular level
© Honkala et al; licensee BioMed Central Ltd. 2009
Received: 19 February 2009
Accepted: 28 April 2009
Published: 28 April 2009
Hydrolethalus syndrome (HLS) is a severe fetal malformation syndrome characterized by multiple developmental anomalies, including central nervous system (CNS) malformation such as hydrocephaly and absent midline structures of the brain, micrognathia, defective lobation of the lungs and polydactyly. Microscopically, immature cerebral cortex, abnormalities in radial glial cells and hypothalamic hamartoma are among key findings in the CNS of HLS fetuses. HLS is caused by a substitution of aspartic acid by glycine in the HYLS1 protein, whose function was previously unknown.
To provide insight into the disease mechanism(s) of this lethal disorder we have studied different aspects of HLS and HYLS1. A genome-wide gene expression analysis indicated several upregulated genes in cell cycle regulatory cascades and in specific signal transduction pathways while many downregulated genes were associated with lipid metabolism. These changes were supported by findings in functional cell biology studies, which revealed an increased cell cycle rate and a decreased amount of apoptosis in HLS neuronal progenitor cells. Also, changes in lipid metabolism gene expression were reflected by a significant increase in the cholesterol levels of HLS liver tissues. In addition, based on our functional studies of HYLS1, we propose that HYLS1 is a transcriptional regulator that shuffles between the cytoplasm and the nucleus, and that when HYLS1 is mutated its function is significantly altered.
In this study, we have shown that the HYLS1 mutation has significant consequences in the cellular and tissue levels in HLS fetuses. Based on these results, it can be suggested that HYLS1 is part of the cellular transcriptional regulatory machinery and that the genetic defect has a widespread effect during embryonic and fetal development. These findings add a significant amount of new information to the pathogenesis of HLS and strongly suggest an essential role for HYLS1 in normal fetal development.
Hydrolethalus syndrome (HLS, MIM 236680) is an autosomally recessively inherited developmental malformation syndrome leading to stillbirth or death shortly after birth. HLS is characterized by a severe central nervous system (CNS) malformation with hydrocephaly and absent midline structures of the brain. The main neuropathological findings include a unique open-book appearance of the brain midline, the 'key-hole' defect in the base of the scull, a massive accumulation of cerebrospinal fluid, a dysplastic cortex, agenesis of the hippocampi, hypoplastic cerebellum and brain stem as well as hypothalamic hamartoma. Microscopically, disrupted and abnormal radial glial formation can be seen, as well as a severely disorganized cortex with abundant primitive neuroepithelial rosettes . Other clinical features include micrognathia, polydactyly of hands and feet, and defective lobation of the lungs. In addition, the amount of amniotic fluid is increased, with case reports of up to eight liters at birth [2, 3]. Nowadays, HLS can be effectively detected by ultrasound scan, usually in the end of the first trimester of the pregnancy . HLS is enriched in the Finnish population with an incidence of at least 1:20,000 .
Our earlier studies have revealed a missense mutation in a novel gene HYLS1 as a causative mutation for HLS . This mutation is an A to G transition leading to a substitution of aspartic acid 211 to glycine (D211G) in the 299 amino acid polypeptide. HYLS1 consists of six exons with five known splice variants, but only the last exon encodes for the protein. HYLS1 was seen to have a wide expression pattern when human fetal cDNAs were studied and the same was observed in mouse embryonic in situ studies. When the cellular localization of the HYLS1 protein was studied in an overexpression cell model we detected the partially different localization of wild-type (wt) and mutant forms of the protein. While the wt form localizes mainly into the cytoplasm, the mutated form partly accumulates in the nucleus forming dot-like structures . The function of the HYLS1 protein is not known and it lacks any known functional domains except a low-complexity region. In addition, the protein is not homologous with any known protein family. However, the polypeptide has orthologs among other species with a conserved polypeptide domain where the mutation site is located .
In this study, we have had an exceptional opportunity to investigate several cell and tissue samples from HLS cases and healthy control fetuses with different methods in order to understand the disease mechanism(s) of this grievous disorder. In addition, we have obtained important novel information about the function of the normal and mutant HYLS1 protein which has a critical role during fetal development.
Disease pathogenesis of HLS
Owing the dramatic phenotype of HLS fetuses and the lack of exact information on HYLS1 function, we performed genome-wide gene expression analysis of fetal skin fibroblast cell lines (HLS N = 3, control N = 4) to obtain novel data on cellular pathways influencing the HLS pathogenesis. The quality control of the samples showed that the control and HLS samples were distinctly assigned to their own clusters. At the end, we obtained a total of 802 transcripts to evaluate by analysis of variance (ANOVA; t-test) statistical testing and as a result, we chose a statistically significant subgroup of these to be analyzed further.
Proliferation assay and analysis of apoptosis rate
Cholesterol level measurement
Functional studies of HYLS1
Nuclear export study
HLS is a severe fetal malformation syndrome with a wide spectrum of phenotypic features and with the pathogenic mutation situated in a gene with no previously known function. Therefore, we used a combination of several different research methods to unravel the disease pathogenesis behind this lethal syndrome as well as to shed light on the role of the HYLS1 protein during fetal development.
As described earlier, the structural pattern of the brain is severely disturbed in HLS fetuses both at the macroscopic and the microscopic level . Frequent findings include the absence of the midline structures, a severely disorganized cortex, disrupted and abnormal formation of radial glial cells, as well as formation of primitive neuroepithelial rosettes. In current cellular studies, HLS neuronal progenitor cells showed a significantly increased proliferation rate while the amount of apoptosis was decreased. These findings are highly interesting because apoptosis is an essential and precisely controlled phenomenon of controlled cell death both in fetal development and in adulthood. When creating animal models with suppressed apoptosis rate, in many cases genetic reduction or elimination of cell death led to gross anatomical malformations or embryonic mortality, in some cases probably as a result of continued proliferation of undead cells . This result nicely supports the reduced amount of apoptosis in HLS cells and further, the dramatic phenotype of the CNS and other malformations seen in HLS. Still, the relationship between the reduced rate of apoptosis and the elevated proliferation rate needs additional studies in order to explain the interaction of these findings and to understand the mechanism causing the severe malformations in the brain. It would be beneficial to clarify whether one of these phenomena is the primary and the other the secondary symptom occurring during the abnormal brain development in HLS.
Among other interesting results in microarray analysis, neuropilin 2 was found to be downregulated by over three-fold in HLS cells. Neuropilins function as receptors for some of the semaphorins, semaphorins in turn acting as chemorepulsive signal in interneuron migration during development of the brain cortex. Marin et al used a mouse model to demonstrate that interneurons expressing neuropilins avoid entering the striatum because of this repulsive signal and are thus directed to the cortex . Loss of neuropilin function, in turn, increases the number of interneurons that migrate into the striatum. When the expression level of neuropilins is decreased, the correct migration pattern of interneurons could also be compromised in the brain of the HLS cases. Thus, the expression array result corresponds well with the findings of disrupted brain architecture in our previous studies . Although highly speculative at the moment, the observed upregulation of CCND1, in turn, might in its part explain the hamartoma finding in HLS fetuses since abnormal expression levels of CCND1 have been linked with development of cancer . Also, in a recent report, intestinal cell kinase (ICK) was found to be mutated in a syndrome sharing some overlapping symptoms with HLS and ICK was suggested to be involved in cell-cycle regulation and apoptosis during mammalian development . This is of interest as kinases are crucial in several cellular functions including signal transduction and since several genes related to signal transduction and further, some genes associated with the protein kinase cascade, were upregulated in HLS neuronal progenitor cells.
When comparing HLS with other fetal malformation syndromes, Pallister-Hall syndrome (PHS, MIM 146510) [11, 12] that is caused by mutations in the GLI3 gene [13–15], probably has the most resemblance to HLS. The shared features between HLS and PHS are polydactyly, micrognathia, occasional cleft/lip palate, abnormal lobation of lungs, heart defects and hypothalamic hamartoma. GLI3 is a transcription factor of the Sonic hedgehog (SHH) pathway and Gli3 deficient mice have been shown to have a disorganized radial glia structure in the brain cortex , the condition also seen in the brain of HLS cases . Another syndrome resembling HLS is Smith-Lemli-Opitz syndrome (SLOS, MIM 270400) [17, 18]. SLOS has a wide spectrum of phenotypic features ranging from a mild disorder with learning and behavioral problems to a lethal malformation syndrome. Prominent features of the syndrome include growth retardation, microcephaly, holoprosencephaly, ptosis, micrognathia, cleft palate and postaxial polydactyly. SLOS is caused by the mutations in the DHCR7 gene [19, 20]. These mutations lead to increased levels of 7-dehydrocholesterol and decreased cholesterol levels in patient serum  while interestingly in our gene expression arrays, DHCR7 was downregulated by almost three-fold when compared with the wt cells. Also, increased cholesterol levels were observed in HLS liver samples. In addition to DHCR7 the microarray analysis revealed other genes such as HMGCS1, ACAT2 and LDLR involved in the cholesterol metabolism that were downregulated. These results suggest that build-up of cholesterol in the liver causes feedback downregulation of these genes involved in the cholesterol metabolism or receptor-mediated endocytosis of cholesterol in the form of low-density lipoprotein (LDL) particles from the circulation.
Since PHS and SLOS share several similar features with HLS there is a possibility that HYLS1 is involved in similar kinds of molecular pathways as proteins behind these syndromes. Thus, it is tempting to hypothesize that HYLS1 directly or indirectly affects the function of the SHH signaling pathway. Since HYLS1 has significant transactivational capacity it could function as a transcriptional regulator in some stage of the SHH pathway as GLI3 does. On the other hand, as several genes related to lipid metabolism show downregulation in HLS cells and as SHH protein is dependent on cholesterol to function properly, HYLS1 could function indirectly in SHH signaling via cholesterol metabolism pathway instead of being directly part of the SHH pathway.
As a result of the essential new studies in cellular level, we found out that the transcriptional activity of HYLS1 is significantly decreased when mutated. In addition, we know that the subcellular localization differs between wt and mutant forms of HYLS1. Based on these results, it can be hypothesized that HYLS1 is a part of the transcription regulatory machinery and that different results between the wt and the mutant protein are a result of the conformational change in protein structure caused by the amino acid substitution. It still remains to be solved whether the amino acid change results in difficulty in the exportation of HYLS1 from the nucleus to cytoplasm, which disturbs the function of the protein. Another possibility is that the mutated HYLS1 is unable to reach the activity level required for normal function and this leads to disturbed downstream pathway regulation or that the possible conformational change in the mutated form of HYLS1 somehow disturbs normal developmental pathway(s) when it is mutated and, thus, leads to the extensive amount of severe symptoms.
In this study, we have demonstrated through several analyses the significant consequences that the HYLS1mutation causes in the cellular and tissue levels. As a conclusion, we suggest that HYLS1 is a transcriptional regulator functioning in central pathway(s) related to fetal developmental processes. The results presented here add a significant amount of new information of the HLS pathogenesis and although the subject of the study is a rare malformation syndrome, these findings strongly suggest an essential role for HYLS1 in normal fetal development.
Subjects and samples
This study has been approved by the ethical committees of Joint Authority for the Hospital District of Helsinki and Uusimaa, Finland. The controls were age-matched healthy fetuses aborted for social reasons. The parents' consent was obtained for the collection and study of the autopsy samples.
Embryonic skin fibroblast cells obtained from the control and HLS fetuses as well as commercial human embryonic kidney cell line (HEK-293) were cultured as monolayers in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% bovine calf serum, 100 units/ml penicillin and 100 units/ml streptomycin. SH-SY5Y human neuroblastoma cells were cultured as monolayers in 1:1 mixture of Ham's F12 and DMEM supplemented with 10% bovine calf serum, 100 units/ml penicillin, 100 units/ml streptomycin and 0.1% nonessential amino acids. In order to obtain neuronal progenitor cells, cortical biopsies were collected at autopsy. The autopsy was performed for each fetus within 5 hours of delivery. Neuronal progenitor cell lines were initiated by homogenizing brain tissue with pipetting and filtering prior to culture. The cells were cultured as neurospheres in serum free progenitor cell medium, consisting of DMEM supplemented with 20 ng/ml of basic fibroblast growth factor (FGF, Sigma-Aldrich, St. Louis, MO, USA), 40 ng/ml of epidermal growth factor (EGF, Sigma-Aldrich) and 10 ng/ml of leukemia inhibitory factor (LIF, Chemicon International, Temecula, CA, USA). All cells were maintained at +37°C in a 5% CO2 atmosphere.
Microarray analysis was performed according to the Affymetrix standard protocol (Affymetrix, Santa Clara, California, USA). In brief, total RNA was extracted with Trizol reagent (Invitrogen, Carlsbad, California, USA) and RNeasy Mini kit (Qiagen, Venlo, the Netherlands). Quantity of the RNA was determined with UV-spectrometry and the quality was controlled with the Agilent Bioanalyzer 2100 (Agilent Technologies, Palo Alto, California, USA). The cRNA was fragmented and hybridized to Affymetrix HG-U133 Plus 2.0 chips (Affymetrix) as described in the protocol. Post-hybridization procedures including washing, staining and scanning were performed according to the Affymetrix protocol.
Analysis of gene expression data
Cell intensity files (CEL) and chip files (CHP) were generated from images of the scanned arrays using Affymetrix Gene Chip Operating Software (Affymetrix) with the default settings recommended by the manufacturer. The CEL files are accessible through the ArrayExpress accession E-MEXP-1900 . All further data processing was carried out using the GeneSpring 7.1 data analysis software (Silicon Genetics, Redwood City, California, USA). CEL files were normalized using the GC-RMA algorithm  with default settings, while the cross gene error model implemented in GeneSpring was used to determine cut-offs for lowest reliable signal intensities. The expression level of each gene was then equally scaled through median centering. Unreliable data was filtered out using a filtering strategy based on Affymetrix detection calls, which were extracted from the CHP files and imported into GeneSpring. In order to pass the filter genes had to score a marginal or present call in all arrays, or absent in all arrays pertaining to one condition while marginal or present in all arrays of the other condition. Hierarchical clustering, based on average linkage and Pearson's correlation, and principal component analysis (PCA) were performed to identify arrays with outlier behavior, compared with their biological replicates representing the same condition. A two-step process was employed to identify differentially expressed genes. First, genes with less-prominent changes in gene expression between affected subjects and controls were excluded by requiring a fold change of at least two. The remaining genes were tested for statistically significant changes in expression using Student's t-test for independent samples. We corrected p-values to account for multiple testing using the method of Benjamini and Hochberg , using a 12% false discovery rate as a cut-off for significance. Lists of significantly up/downregulated genes were examined for biologically relevant associations using the web-based gene set analysis toolkit WebGestalt [25, 26].
In vitro study of the neuronal progenitor cell proliferation was performed using the BrdU labeling method. Neuronal precursor cells (HLS N = 1, control N = 2) maintained in culture were supplied with 1:1,000 BrdU (Amersham Biosciences UK Limited, Buckinghamshire, England) and kept in nondifferentiating media for 12–15 hours. After incubation the cells were attached to coverslips with a cytospin centrifuge and fixed with 4% PFA for 20 minutes. The BrdU positive cells were stained using the BrdU antibody kit (RPN 202, Amersham Biosciences). The ratio between the whole cell content and the amount of proliferating cells was counted. The experiment was repeated three times and all samples were prepared in duplicate. Samples were grown in several aliquots and pooled together for the analysis to minimize the effects of passage and aliquot differences. Stained cells were analyzed with a Zeiss Axioplan 2 fluorescence microscope.
Analysis of apoptosis rate
The amount of apoptosis was measured by Annexin-V-Fluos staining kit (Roche, Basel, Switzerland). Undifferentiated neurospheres, each sample (HLS N = 1, control N = 2) containing approximately 1 × 106 cells were harvested, dissociated into single cells and double stained with FITC-conjugated annexin (FA) and propidiumiodide (PI) for 15 minutes at room temperature and diluted (1:50 both) into HEPES buffer according to the manufacturer's protocol. Negative controls were treated by the same way but without one of the appropriate stainings (only FA or PI). Cells exposed to UV-light, dexamethasone or hydroxyurea were used as positive controls to ensure functionality of the assay. Unspecific labeling of FITC was excluded by treating the cells with IgG-conjugated FITC. Annexin labels both apoptotic and necrotic cells while living cells remain unstained. Necrotic cells were excluded by PI staining, which stains DNA of leaky necrotic cells only. The amount of labeled cells was measured by flow cytometry (FACSaria, BD Biosciences, San Jose, California, USA). Measurements were repeated altogether nine times for control cells and seven times for HLS cells.
Cholesterol and phospolipid level measurement
Cholesterol and phospholipid levels were measured from fetal liver tissue from two healthy controls and two HLS fetuses. Total lipids were extracted from whole liver homogenates using the Folch extraction . Briefly, frozen liver tissue was cut into 5–15 mg pieces and homogenized in a 2:1 methanol-chloroform solvent. Homogenization was performed with Precellys 24 homogenizer (Bertin technologies, Montigny-le-Bretonneux, France) according to the manufacturer's protocol with slight modifications. The homogenized media were centrifuged briefly to separate out the cell debris. The supernatant with extracted lipids was transferred to methylene chloride-purified Kimax tubes and the solvent was evaporated in a nitrogen atmosphere. The dried lipids were kept at -20°C until lipid assays. The samples were re-dissolved in methanol and cholesterol, phospholipids and triglycerides were analyzed in triplicates according to the manufacturer's protocol (Roche/Hitachi, Basel, Switzerland for cholesterol and triglycerides, Wako, Neuss, Germany for phospholipids).
Nuclear export study
In nuclear export studies, HEK-293 cells were transfected in the following manner: 1 × 106 cells were grown on coverslips in six-well plates and transfected with 1 μg of the appropriate expression vector, containing either wt or mut HYLS1 with the Myc sequence immediately before the start codon. LMB (Tocris Bioscience, Bristol, UK) was added to cells 24 hour post-transfection initially at 5, 10, 15 or 20 ng/ml, the cells were grown for 3, 6 or 24 hours and stained as described below. In subsequent experiments, 15 ng/ml LMB was used. Transfections of each individual vector were performed in duplicate and the study was repeated three times. For immunofluorescence studies, cells were fixed with 4% paraformaldehyde (PFA) in phosphate buffered saline (PBS; pH 7.3) at room temperature (RT) for 10 minutes and blocked and permeabilized with 0.2% saponin/0.5% bovine serum albumin (BSA) in PBS. Cells were then incubated with primary antibody (mouse anti-c-myc, Santa Cruz Biotechnology, Santa Cruz, California, USA) for 1 hour at RT. After washing, cells were incubated with anti-mouse Texas Red secondary antibody for 40 minutes at RT. After final washes, cells were mounted onto microscope slides with Vectashield hard set mounting medium containing 4',6-diamidino-2-phenylindole (DAPI; Vector Laboratories) and the data was acquired using an Axioplan Z imaging fluorescence microscope and AxioVision Rel. 4.6 program. The proportion of cells showing either cytoplasmic, nuclear or combined cytoplasmic and nuclear staining was calculated.
SH-SY5Y cells were seeded onto 12-well plates at 1.2 × 105 cells per well. The cells were transfected 24 hours after seeding with 750 ng of wt or mutant human HYLS1 cloned in fusion with Gal4-DBD. In all transfections, 200 ng of reporter vector pG5-LUC (Promega, Mannheim, Germany) containing Gal4 binding sites was used. The pM1 vector was used as a negative control. The transfections were performed using the Fugene HD transfection reagent (Roche) according the manufacturer's instructions. The cells were harvested 48 hours after transfection and the luciferase activity was determined using the Luciferase Assay System (Promega). The luciferase activities were normalized according to the total protein concentration of the lysates which were determined by biuret reaction (Novagen, Madison, Wisconsin, USA). All transfections were performed in triplicate and repeated three times.
Dr Tanja Ilmarinen is acknowledged for valuable help in the methodology of the transactivation assay and so is Professor Leena Peltonen for her contribution to this project. Katriina Hautaviita, Lea Puhakka, Anne Vikman, Kaija Antila and Sari Nuutinen are thanked for excellent technical assistance. Heidi Nousiainen is acknowledged for language revision of the manuscript. We also thank the HLS families for participating in this study.
This study was supported by the Academy of Finland grants 211124 and 118468 (MK), Helsinki Biomedical Graduate School (HH), the Research Foundation of the University of Helsinki (HH), Sigrid Juselius Foundation (MK) and Finnish Foundation for Cardiovascular Research (MJ). The Department of Medical Genetics Väestöliitto (RS) is funded by Finland's Slot Machine Association (RAY).
- Paetau A, Honkala H, Salonen R, Ignatius J, Kestilä M, Herva R: Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis. J Neuropathol Exp Neurol. 2008, 67: 750-762. 10.1097/NEN.0b013e318180ec2e.View ArticlePubMedGoogle Scholar
- Salonen R, Herva R, Norio R: The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients. Clin Genet. 1981, 19: 321-330.View ArticlePubMedGoogle Scholar
- Salonen R, Herva R: Hydrolethalus syndrome. J Med Genet. 1990, 27: 756-759. 10.1136/jmg.27.12.756.PubMed CentralView ArticlePubMedGoogle Scholar
- Ämmälä P, Salonen R: First-trimester diagnosis of hydrolethalus syndrome. Ultrasound Obstet Gynecol. 1995, 5: 60-62. 10.1046/j.1469-0705.1995.05010060.x.View ArticlePubMedGoogle Scholar
- Mee L, Honkala H, Kopra O, Vesa J, Finnilä S, Visapää I, Sang TK, Jackson GR, Salonen R, Kestilä M, Peltonen L: Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1. Hum Mol Genet. 2005, 14: 1475-1488. 10.1093/hmg/ddi157.View ArticlePubMedGoogle Scholar
- Yoneda Y: Nucleocytoplasmic protein traffic and its significance to cell function. Genes Cells. 2000, 5: 777-787. 10.1046/j.1365-2443.2000.00366.x.View ArticlePubMedGoogle Scholar
- Buss RR, Sun W, Oppenheim RW: Adaptive roles of programmed cell death during nervous system development. Annu Rev Neurosci. 2006, 29: 1-35. 10.1146/annurev.neuro.29.051605.112800.View ArticlePubMedGoogle Scholar
- Marin O, Yaron A, Bagri A, Tessier-Lavigne M, Rubenstein JL: Sorting of striatal and cortical interneurons regulated by semaphorin-neuropilin interactions. Science. 2001, 293: 872-875. 10.1126/science.1061891.View ArticlePubMedGoogle Scholar
- Tashiro E, Tsuchiya A, Imoto M: Functions of cyclin D1 as an oncogene and regulation of cyclin D1 expression. Cancer Sci. 2007, 98: 629-635. 10.1111/j.1349-7006.2007.00449.x.View ArticlePubMedGoogle Scholar
- Lahiry P, Wang J, Robinson JF, Turowec JP, Litchfield DW, Lanktree MB, Gloor GB, Puffenberger EG, Strauss KA, Martens MB, Ramsay DA, Rupar CA, Siu V, Hegele RA: A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systems. Am J Hum Genet. 2009, 84: 134-147. 10.1016/j.ajhg.2008.12.017.PubMed CentralView ArticlePubMedGoogle Scholar
- Hall JG, Pallister PD, Clarren SK, Beckwith JB, Wiglesworth FW, Fraser FC, Cho S, Benke PJ, Reed SD: Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly – a new syndrome? Part I: clinical, causal, and pathogenetic considerations. Am J Med Genet. 1980, 7: 47-74. 10.1002/ajmg.1320070110.View ArticlePubMedGoogle Scholar
- Clarren SK, Alvord EC, Hall JG: Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly – a new syndrome? Part II: Neuropathological considerations. Am J Med Genet. 1980, 7: 75-83. 10.1002/ajmg.1320070111.View ArticlePubMedGoogle Scholar
- Kang S, Graham JM, Olney AH, Biesecker LG: GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome. Nat Genet. 1997, 15: 266-268. 10.1038/ng0397-266.View ArticlePubMedGoogle Scholar
- Johnston JJ, Olivos-Glander I, Killoran C, Elson E, Turner JT, Peters KF, Abbott MH, Aughton DJ, Aylsworth AS, Bamshad MJ, Booth C, Curry CJ, David A, Dinulos MB, Flannery DB, Fox MA, Graham JM, Grange DK, Guttmacher AE, Hannibal MC, Henn W, Hennekam RC, Holmes LB, Hoyme HE, Leppig KA, Lin AE, Macleod P, Manchester DK, Marcelis C, Mazzanti L, McCann E, McDonald MT, Mendelsohn NJ, Moeschler JB, Moghaddam B, Neri G, Newbury-Ecob R, Pagon RA, Phillips JA, Sadler LS, Stoler JM, Tilstra D, Walsh Vockley CM, Zackai EH, Zadeh TM, Brueton L, Black GC, Biesecker LG: Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. Am J Hum Genet. 2005, 76: 609-622. 10.1086/429346.PubMed CentralView ArticlePubMedGoogle Scholar
- Kang S, Allen J, Graham JM, Grebe T, Clericuzio C, Patronas N, Ondrey F, Green E, Schaffer A, Abbott M, Biesecker LG: Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndrome. J Med Genet. 1997, 34: 441-446. 10.1136/jmg.34.6.441.PubMed CentralView ArticlePubMedGoogle Scholar
- Friedrichs M, Larralde O, Skutella T, Theil T: Lamination of the cerebral cortex is disturbed in Gli3 mutant mice. Dev Biol. 2008, 318: 203-214. 10.1016/j.ydbio.2008.03.032.View ArticlePubMedGoogle Scholar
- Smith DW, Lemli L, Opitz JM: A newly recognized syndrome of multiple congenital anomalies. J Pediatr. 1964, 64: 210-217. 10.1016/S0022-3476(64)80264-X.View ArticlePubMedGoogle Scholar
- Porter FD: Smith-Lemli-Opitz syndrome: pathogenesis, diagnosis and management. Eur J Hum Genet. 2008, 16: 535-541. 10.1038/ejhg.2008.10.View ArticlePubMedGoogle Scholar
- Wassif CA, Maslen C, Kachilele-Linjewile S, Lin D, Linck LM, Connor WE, Steiner RD, Porter FD: Mutations in the human sterol delta7-reductase gene at 11q12–13 cause Smith-Lemli-Opitz syndrome. Am J Hum Genet. 1998, 63: 55-62. 10.1086/301936.PubMed CentralView ArticlePubMedGoogle Scholar
- Waterham HR, Wijburg FA, Hennekam RC, Vreken P, Poll-The BT, Dorland L, Duran M, Jira PE, Smeitink JA, Wevers RA, Wanders RJ: Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene. Am J Hum Genet. 1998, 63: 329-338. 10.1086/301982.PubMed CentralView ArticlePubMedGoogle Scholar
- Tint GS, Irons M, Elias ER, Batta AK, Frieden R, Chen TS, Salen G: Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz syndrome. N Engl J Med. 1994, 330: 107-113. 10.1056/NEJM199401133300205.View ArticlePubMedGoogle Scholar
- Array Express accession E-MEXP-1900. [http://www.ebi.ac.uk/microarray-as/ae/]
- Wu Z, Irizarry RA: Stochastic models inspired by hybridization theory for short oligonucleotide arrays. J Comput Biol. 2005, 12: 882-893. 10.1089/cmb.2005.12.882.View ArticlePubMedGoogle Scholar
- Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc B. 1995, 57: 289-300.Google Scholar
- Zhang B, Kirov S, Snoddy J: WebGestalt: an integrated system for exploring gene sets in various biological contexts. Nucleic Acids Res. 2005, 33: W741-W748. 10.1093/nar/gki475.PubMed CentralView ArticlePubMedGoogle Scholar
- WebGestalt: web-based gene set analysis toolkit. [http://bioinfo.vanderbilt.edu/webgestalt/]
- Folch J, Lees M, Sloane Stanley GH: A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957, 226: 497-509.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.