Comparative analysis of the ETV6 gene in vertebrate genomes from pufferfish to human

被引:10
|
作者
Montpetit, A
Sinnett, D
机构
[1] Hop St Justine, Div Hematol Oncol, Charles Bruneau Canc Ctr, Montreal, PQ H3T 1C5, Canada
[2] Univ Montreal, Dept Biochem, Montreal, PQ H3C 3J7, Canada
[3] Univ Montreal, Dept Pediat, Montreal, PQ H3C 3J7, Canada
基金
英国医学研究理事会;
关键词
ETV6; transcription factor; comparative genetics; vertebrate genomes; Fugu rubripes;
D O I
10.1038/sj.onc.1204444
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ETV6 gene encodes an Ets-like transcription factor that is frequently rearranged in leukemias. While some of the functions of ETV6 have been uncovered recently, little is known about the key structural elements involved. Comparative genome analysis may provide novel insights into gene evolution and functions. In this study, me cloned and sequenced the homologue of ETV6 from the compact genome of the pufferfish Fugu rubripes (fETV6). The genomic structure of the fETV6 gene was investigated by sequence analysis of a contig of genomic clones. The fETV6 gene, composed of eight exons, spans about 15 kb and is 16 times smaller than its human counterpart mainly because of the reduced intron size. Three of the seven introns of fETV are unusually large (more than 2 kb), including the 8.2 kb intron 2. The gene codes for a protein of 465 amino acids that is highly related to its human homologue, exhibiting an overall identity of 58% (72% similarity). To investigate the functional and evolutionary aspects of ETV6, we undertook a comparative analysis of this gene from various vertebrates (human, mouse, chicken, zebrafish and Fugu). As expected, the PNT and ETS domains were highly conserved, with on average 81 and 95% peptide sequence identity, respectively. In addition, we found several new highly conserved regions within the central section of the protein that are likely to represent further functional or structural domains, which may be associated with the transcription repression capacity of this protein. We also found conserved putative regulatory elements in the promoter as well as in the large intron 2 of fETV6. The information derived from this comparative analysis will serve as the basis for more precise functional studies of ETV6 gene regulation and function.
引用
收藏
页码:3437 / 3442
页数:6
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