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Brain stem global gene expression profiles in human spina bifida embryos

Brain stem global gene expression profiles in human spina bifida embryos
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摘要 Environmental and genetic factors influence the occurrence of neural tube defects, such as spina bifida. Specific disease expression patterns will help to elucidate the pathogenesis of disease. However, results obtained from animal models, which often exhibit organism specificity, do not fully explain the mechanisms of human spina bifida onset. In the present study, three embryos with a gestational age of approximately 17 weeks and a confirmed diagnosis of spina bifida, as well as 3 age-matched normal embryos, were obtained from abortions. Fetal brain stem tissues were dissected for RNA isolation, and microarray analyses were conducted to examine profiles of gene expression in brain stems of spina bifida and normal embryos using Affymetrix HG-U133A 2.0 GeneChip arrays. Of the 14 500 gene transcripts examined, a total of 182 genes exhibited at least 2.5-fold change in expression, including 140 upregulated and 42 downregulated genes. These genes were placed into 19 main functional categories according to the Gene Ontology Consortium database for biological functions. Of the 182 altered genes, approximately 50% were involved in cellular apoptosis, growth, adhesion, cell cycle, stress, DNA replication and repair, signal transduction, nervous system development, oxidoreduction, immune responses, and regulation of gene transcription. Gene expression in multiple biological pathways was altered in the brain stem of human spina bifida embryos. Environmental and genetic factors influence the occurrence of neural tube defects, such as spina bifida. Specific disease expression patterns will help to elucidate the pathogenesis of disease. However, results obtained from animal models, which often exhibit organism specificity, do not fully explain the mechanisms of human spina bifida onset. In the present study, three embryos with a gestational age of approximately 17 weeks and a confirmed diagnosis of spina bifida, as well as 3 age-matched normal embryos, were obtained from abortions. Fetal brain stem tissues were dissected for RNA isolation, and microarray analyses were conducted to examine profiles of gene expression in brain stems of spina bifida and normal embryos using Affymetrix HG-U133A 2.0 GeneChip arrays. Of the 14 500 gene transcripts examined, a total of 182 genes exhibited at least 2.5-fold change in expression, including 140 upregulated and 42 downregulated genes. These genes were placed into 19 main functional categories according to the Gene Ontology Consortium database for biological functions. Of the 182 altered genes, approximately 50% were involved in cellular apoptosis, growth, adhesion, cell cycle, stress, DNA replication and repair, signal transduction, nervous system development, oxidoreduction, immune responses, and regulation of gene transcription. Gene expression in multiple biological pathways was altered in the brain stem of human spina bifida embryos.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2011年第5期366-372,共7页 中国神经再生研究(英文版)
基金 Supported by the National Key Project of Scientific and Technical Supporting Programs funded by the Ministry of Science & Technology of China, No. 2007BA107A02 the National Basic Research Program of China (973 Program), No. 2007CB511902 the Shanxi Scholarship Council of China, No. 2008-48 the Shanxi Natural Science Foundation, No. 2010011049-2 the National Natural Science Foundation of China, No. 31040056
关键词 APOPTOSIS GENECHIP gene expression neural tube defect spina bifida apoptosis GeneChip gene expression neural tube defect spina bifida
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  • 1Botto LD, Moore CA, Khoury M J, et al. Neural-tube defects. N Engl J Med. 1999;341(20):1509-1519.
  • 2Detrait ER, George TM, Etchevers HC, et al. Human neural tube defects: developmental biology, epidemiology, and genetics. Neurotoxicol Teratol. 2005;27(3):515-524.
  • 3Gu X, Lin L, Zheng X, et al. High prevalence of NTDs in Shanxi Province: a combined epidemiological approach. Birth Defects Res A Clin Mol Teratol. 2007;79(10):702-707.
  • 4Jiang B, Kumar SD, Loh WT, et al. Global gene expression analysis of cranial neural tubes in embryos of diabetic mice. J Neurosci Res. 2008;86(16):3481-3493.
  • 5Copp A J, Greene ND. Genetics and development of neural tube defects. J Pathol. 2010;220(2):217-230.
  • 6Cecconi F, Piacentini M, Fimia GM. The involvement of cell death and survival in neural tube defects: a distinct role for apoptosis and autophagy? Cell Death Differ. 2008; 15(7): 1170-1177.
  • 7Juriloff DM, Harris MJ. Mouse models for neural tube closure defects. Hum Mol Genet. 2000;9(6):993-1000.
  • 8Volcik KA, Blanton SH, Kruzel MC, et al. Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects. Am J Med Genet. 2002; 110(3):203-207.
  • 9Richter B, Schultealbert AH, Koch MC. Human T and risk for neural tube defects. J Med Genet. 2002;39(3):E14.
  • 10Chatkupt S, Hol FA, Shugart YY, et al. Absence of linkage between familial neural tube defects and PAX3 gene. J Med Genet. 1995;32(3):200-204.

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