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Evolutionary constraints on the disrupted in schizophrenia locus
被引:75
作者:
Taylor, MS
Devon, RS
Millar, JK
Porteous, DJ
机构:
[1] Univ Edinburgh, Med Genet Sect, Mol Med Ctr, Edinburgh EH4 2XU, Midlothian, Scotland
[2] MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
来源:
基金:
英国医学研究理事会;
关键词:
alternative splicing;
DNA;
intergenic;
genetic predisposition to disease;
genomics;
mental disorders;
RNA splice sites;
schizophrenia;
synteny;
translocation (genetics);
D O I:
10.1016/S0888-7543(02)00026-5
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The Disrupted in Schizophrenia (DISC) locus on human chromosome 1q42 has been strongly implicated by genetic studies as a susceptibility locus for major mental illnesses. In humans the locus is transcriptionally complex, with multiple alternate splicing events, antisense transcription, and intergenic splicing all evident. We have compared the genomic sequence and transcription maps of this locus between human, mouse, pufferfish (Fugu rubripes), and, in part, zebrafish (Danio rerio). The order and orientation of EGLN1, TSNAX, and DISC1 genes are conserved between mammals and F. rubripes. Intergenic splicing and short intergenic transcripts are not found to be conserved features. DISC2, a putative noncoding transcript partially antisense to DISC1, is not conserved in mouse or F. rubripes. Alternate splice forms of the protein-coding DISC1 gene are conserved even though the genomic structure is not. The amino acid sequence of DISCI is diverging rapidly, although a putative nuclear localization signal and discrete blocks of coiled coil are specifically conserved features. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:67 / 77
页数:11
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