Maternal ABCA1 genotype is associated with severity of Smith–Lemli–Opitz syndrome and with viability of patients homozygous for null mutations (original) (raw)
Smith DW, Lemli L, Opitz JM : A newly recognized syndrome of multiple congenital anomalies. J Pediatr 1964; 64: 210–217. ArticleCAS Google Scholar
Kelley RI, Hennekam RC : The Smith–Lemli–Opitz syndrome. J Med Genet 2000; 37: 321–335. ArticleCAS Google Scholar
Witsch-Baumgartner M, Fitzky BU, Ogorelkova M et al. Mutational spectrum in the delta7-sterol reductase gene and genotype–phenotype correlation in 84 patients with Smith–Lemli–Opitz syndrome. Am J Hum Genet 2000; 66: 402–412. ArticleCAS Google Scholar
Witsch-Baumgartner M, Schwentner I, Gruber M et al. Age and origin of major Smith–Lemli–Opitz syndrome (SLOS) mutations in European populations. J Med Genet 2008; 45: 200–209. ArticleCAS Google Scholar
Irons M, Elias ER, Salen G, Tint GS, Batta AK : Defective cholesterol biosynthesis in Smith–Lemli–Opitz Syndrome. Lancet 1993; 341: 1414. ArticleCAS Google Scholar
Fitzky BU, Witsch-Baumgartner M, Erdel M et al. Mutations in the delta7-sterol reductase gene in patients with the Smith–Lemli–Opitz syndrome. Proc Natl Acad Sci USA 1998; 95: 8181–8186. ArticleCAS Google Scholar
Waterham HR, Wijburg FA, Hennekam RC et al. Smith–Lemli–Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene. Am J Hum Genet 1998; 63: 329–338. ArticleCAS Google Scholar
Wassif CA, Maslen C, Kachilele-Linjewile S et al. Mutations in the human sterol delta7-reductase gene at 11q12–13 cause Smith–Lemli–Opitz syndrome. Am J Hum Genet 1998; 63: 55–56. ArticleCAS Google Scholar
Cooper MK, Wassif CA, Krakowiak PA et al. A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis. Nat Genet 2003; 33: 508–519. ArticleCAS Google Scholar
Cunniff C, Kratz LE, Moser A, Natowicz MR, Kelley RI : Clinical and biochemical spectrum of patients with RSH/Smith–Lemli–Opitz syndrome and abnormal cholesterol metabolism. Am J Med Genet 1997; 68: 263–269. ArticleCAS Google Scholar
Lin DS, Pitkin RM, Connor WE : Placental transfer of cholesterol into the human fetus. Am J Obstet Gynecol 1977; 128: 735–739. ArticleCAS Google Scholar
Farese RV, Ruland SL, Flynn LM, Stokowski RP, Young SG : Knockout of the mouse apolipoprotein B gene results in embryonic lethality in homozygotes and protection against diet-induced hypercholesterolemia in heterozygotes. Proc Natl Acad Sci USA 1995; 92: 1774–1778. ArticleCAS Google Scholar
Witsch-Baumgartner M, Gruber M, Kraft HG et al. Maternal apo E genotype is a modifier of the Smith–Lemli–Opitz syndrome. J Med Genet 2004; 41: 577–584. ArticleCAS Google Scholar
Kuivenhoven JA, de Knijff P, Boer JM et al. Heterogeneity at the CETP gene locus. Influence on plasma CETP concentrations and HDL cholesterol levels. Arterioscler Thromb Vasc Biol 1997; 17: 560–568. ArticleCAS Google Scholar
Shotelersuk V, Ittiwut C, Siriwan P, Angspatt A : Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip. J Med Genet 2003; 40: e64. ArticleCAS Google Scholar
Pezzetti F, Martinelli M, Scapoli L et al. Maternal MTHFR variant forms increase the risk in offspring of isolated nonsyndromic cleft lip with or without cleft palate. Hum Mutat 2004; 4: 104–105. Article Google Scholar
Mauch DH, Nagler K, Schumacher S et al. CNS synaptogenesis promoted by glia-derived cholesterol. Science 2001; 294: 1354–1357. ArticleCAS Google Scholar
Cohen JC, Kiss RS, Pertsemlidis A, Marcel YL, McPherson R, Hobbs HH : Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science 2004; 5685: 869–872. Article Google Scholar
Descamps OS, Bruniaux M, Guilmot PF, Tonglet R, Heller FR : Lipoprotein concentrations in newborns are associated with allelic variations in their mothers. Atherosclerosis 2004; 172: 287–298. ArticleCAS Google Scholar
Tregouet DA, Ricard S, Nicaud V et al. In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarction. Arterioscler Thromb Vasc Biol 2004; 24: 775–781. ArticleCAS Google Scholar
Kolovou V, Kolovou G, Marvaki A et al. ATP-bindig cassette transporter A1 gene polymorphisms and serum lipid levels in young Greek nurses. Lipids Health Dis 2011; 10: 56–63. ArticleCAS Google Scholar
Frikke-Schmidt R, Nordestgaard BG, Jensen GB, Steffensen R, Tybjaerg-Hansen A : Genetic variation in ABCA1 predicts ischemic heart diesease in the general population. Arterioscler Thromb Vasc Biol 2008; 28: 180–186. ArticleCAS Google Scholar
Owen JS : Role of ABC1 gene in cholesterol efflux and atheroprotection. Lancet 1999; 354: 1402–1403. ArticleCAS Google Scholar
Schmitz G, Langmann T : Structure, function and regulation of the ABC1 gene product. Curr Opin Lipidol 2001; 12: 129–140. ArticleCAS Google Scholar
Bodzioch M, Orso E, Klucken J et al. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat Genet 1999; 22: 347–351. ArticleCAS Google Scholar
Frikke-Schmidt R, Nordestgaard BG, Jensen GB, Tybjaerg-Hansen A : Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population. J Clin Invest 2004; 114: 1343–1353. ArticleCAS Google Scholar
Goldenberg A, Chevy F, Bernard C, Wolf C, Cormier-Daire V : Clinical characteristics and diagnosis of Smith–Lemli–Opitz syndrome and tentative phenotype–genotype correlation: report of 45 cases. Arch Pediatr 2003; 10: 4–10. ArticleCAS Google Scholar
Mahley RW, Rall SCE : Apolipoprotein E far more than a lipid transport protein. Annu Rev Genomics Hum Genet 2000; 1: 507–537. ArticleCAS Google Scholar
Utermann G : Apolipoprotein E polymorphism in health and disease. Am Heart J 1987; 113: 433–440. ArticleCAS Google Scholar
Kratz LE, Kelley RI : Prenatal diagnosis of the RSH/Smith–Lemli–Opitz syndrome. Am J Med Genet 1999; 82: 376–381. ArticleCAS Google Scholar
Ciara E, Nowaczyk MJM, Witsch-Baumgartner M et al. DHCR7 mutations and genotype–phenotype correlation in 37 Polish patients with Smith–Lemli–Opitz syndrome. Clin Genet 2004; 66: 517–524. ArticleCAS Google Scholar
Jira PE, Wanders RJ, Smeitink JA et al. Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith–Lemli–Opitz syndrome. Ann Hum Genet 2001; 65: 229–236. ArticleCAS Google Scholar
Correa-Cerro LS, Wassif CA, Waye JS et al. DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith–Lemli–Opitz syndrome. J Med Genet 2005; 42: 350–357. ArticleCAS Google Scholar
Witsch-Baumgartner M, Löffler J, Utermann G : Mutations in the human DHCR7 gene. Hum Mutat 2001; 17: 172–182. ArticleCAS Google Scholar
Szakacs G, Langmann T, Özvegy C et al. Characterization of the ATPase cycle of human ABCA1: Implications for its function as a regulator rather than an active transporter. Biochem Biophys Res Comm 2001; 288: 1258–1264. ArticleCAS Google Scholar
Langmann T, Klucken J, Reil M et al. Molecular cloning of the human ATP-binding cassette transporter 1 (hABC1): evidence for sterol-dependent regulation in macrophages. Biochem Biophys Res Commun 1999; 257: 29–33. ArticleCAS Google Scholar
Nikitina L, Wenger F, Baumann M, Surbek D, Körner M, Albrecht C : Expression and localiation pattern of ABCA1 in diverse human placental primary cells and tissues. Placenta 2011; 32: 420–430. ArticleCAS Google Scholar
Stefulj J, Panzenboeck U, Becker T et al. Human endothelial cells of the placental barrier efficiently deliver cholesterol to the fetal circulation via ABCA1 and ABCG1. Circ Res 2009; 104: 600–608. ArticleCAS Google Scholar
Aye IL, Waddell BJ, Mark PJ, Keelan JA : Placental ABCA1 and ABCG1 transporters efflux cholesterol and protect trophoblasts from oxysterol induced toxicity. Biochim Biophys Acta 2010; 1801: 1013–1024. ArticleCAS Google Scholar
Schmitz G, Grandl M : The molecular mechanism of HDL and associated vesicular trafficking mechanism to mediate cellular lipid homeostasis. Arterioscler Thromb Vasc Biol 2009; 29: 1718–1722. ArticleCAS Google Scholar
Velamakanni S, Wei SL, Janvilisri T, van Veen HW : ABCG transporters: structure, substrate specificities and physiological roles: a brief overview. J Bioenerg Biomembr 2007; 39: 465–471. ArticleCAS Google Scholar
Lindegaard ML, Wassif CA, Vaisman B et al. Characterisation of placental cholesterol transport: ABCA1 is a potential target for in utero therapy of Smith–Lemli–Opitz syndrome. Hum Mol Genet 2008; 17: 3806–3813. ArticleCAS Google Scholar
Christiansen-Weber TA, Voland JR, Wu Y et al. Functional loss of ABCA1 in mice causes severe placental malformation, aberrant lipid distribution, and kidney glomerulonephritis as well as high-density lipoprotein cholesterol deficiency. Am J Pathol 2000; 157: 1017–1029. ArticleCAS Google Scholar
Fujimoto VY, Kane JP, Ishida BY, Bloom MS, Browne RW : High-density lipoprotein metabolism and the human embryo. Hum Reprod Update 2010; 16: 20–38. ArticleCAS Google Scholar
Nowaczyk MJ, Waye JS, Douketis JD : DHCR7 mutation carrier rates and prevalence of the RSH/Smith–Lemli–Opitz syndrome: where are the patients? Am J Med Genet A 2006; 140: 2057–2062. Article Google Scholar