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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2006-12-12
pubmed:abstractText
The chitinase 3-like 1 gene (CHI3L1) is abnormally expressed in the hippocampus of subjects with schizophrenia and may be involved in the cellular response to various environmental events that are reported to increase the risk of schizophrenia. Here, we provide evidence that the functional variants at the CHI3L1 locus influence the genetic risk of schizophrenia. First, using case-control and transmission/disequilibrium-test (TDT) methodologies, we detected a significant association between schizophrenia and haplotypes within the promoter region of CHI3L1 in two independent cohorts of Chinese individuals. Second, the at-risk CCC haplotype (P=.00058 and .0018 in case-control and TDT studies, respectively) revealed lower transcriptional activity (P=2.2 x 10(-7)) and was associated with lower expression (P=3.1 x 10(-5)) compared with neutral and protective haplotypes. Third, we found that an allele of SNP4 (rs4950928), the tagging SNP of CCC, impaired the MYC/MAX-regulated transcriptional activation of CHI3L1 by altering the transcriptional-factor consensus sequences, and this may be responsible for the decreased expression of the CCC haplotype. In contrast, the protective TTG haplotype was associated with a high level of CHI3L1 expression. Our findings identify CHI3L1 as a potential schizophrenia-susceptibility gene and suggest that the genes involved in the biological response to adverse environmental conditions are likely to play roles in the predisposition to schizophrenia.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-10208441, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-10547845, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-10682218, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-10784457, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-11144342, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-11154276, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-11244489, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-11584303, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-11701324, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-11720692, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-11922883, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-12071845, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-12091183, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-12872291, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-12916020, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-13679853, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-14745448, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15015934, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15049300, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15121481, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15288500, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15569925, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15700048, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15740637, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-15771622, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-16077049, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-16234240, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-7729426, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-9551488, http://linkedlifedata.com/resource/pubmed/commentcorrection/17160890-9754621
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0002-9297
pubmed:author
pubmed:issnType
Print
pubmed:volume
80
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
12-8
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:17160890-Adipokines, pubmed-meshheading:17160890-Adult, pubmed-meshheading:17160890-Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, pubmed-meshheading:17160890-Case-Control Studies, pubmed-meshheading:17160890-Cell Line, pubmed-meshheading:17160890-China, pubmed-meshheading:17160890-Female, pubmed-meshheading:17160890-Genes, myc, pubmed-meshheading:17160890-Genetic Predisposition to Disease, pubmed-meshheading:17160890-Glycoproteins, pubmed-meshheading:17160890-Haplotypes, pubmed-meshheading:17160890-Humans, pubmed-meshheading:17160890-Lectins, pubmed-meshheading:17160890-Male, pubmed-meshheading:17160890-Middle Aged, pubmed-meshheading:17160890-Promoter Regions, Genetic, pubmed-meshheading:17160890-Protein Binding, pubmed-meshheading:17160890-Schizophrenia, pubmed-meshheading:17160890-Signal Transduction, pubmed-meshheading:17160890-Transcriptional Activation
pubmed:year
2007
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