Genomic characterization of the RUNX2 gene of Fugu rubripes

被引:26
作者
Eggers, JH
Stock, M
Fliegauf, M
Vonderstrass, B
Otto, F
机构
[1] Univ Freiburg, Med Ctr, Dept Hematol & Oncol, D-79106 Freiburg, Germany
[2] Univ Freiburg, Inst Biol 1, D-79104 Freiburg, Germany
[3] Univ Freiburg, Inst Biol 3, D-79104 Freiburg, Germany
关键词
comparative genetics; runt homology domain; Fugu rubripes; enhancer element; RUNX2; conserved element;
D O I
10.1016/S0378-1119(02)00592-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A 105 kb Fugu rubripes genomic region containing the RUNX2 ortholog (frunx2) was sequenced and analysed. Spanning 32 kb, frunx2 is seven times smaller than its human orthologue (223 kb). By comparison of Fugu and human genomic environment a stretch of conserved synteny, comprising the neighbouring genes on both sides, was identified. Except one exon that is alternatively spliced in human RUNX2, all other seven exons could be identified in frunx2. The predicted protein sequence of frunx2 shows a high degree of sequence conservation compared with RUNX2 (83% identity). Like all human paralogues,frunx2 possesses two promoter regions separated by a large intron. Both promoter regions are conserved between the two species and contain several RUNX binding sites pointing to a self-regulatory function. Three further conserved non-coding regions were identified possibly functioning as enhancer elements for tissue-specific expression of RUNX2. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:159 / 167
页数:9
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