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Genomic Sequence Analysis of Fugu rubripes CFTR and Flanking Genes in a 60 kb Region Conserving Synteny with 800 kb of Human Chromosome 7

机译:在800 kb人类染色体7的60 kb区域中,河豚红CFTR和侧翼基因的基因组序列分析

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摘要

To define control elements that regulate tissue-specific expression of the cystic fibrosis transmembrane regulator (CFTR), we have sequenced 60 kb of genomic DNA from the puffer fish Fugu rubripes (Fugu) that includes the CFTR gene. This region of the Fugu genome shows conservation of synteny with 800-kb sequence of the human genome encompassing the WNT2, CFTR, , and CBP90 genes. Additionally, the genomic structure of each gene is conserved. In a multiple sequence alignment of human, mouse, and Fugu, the putative WNT2 promoter sequence is shown to contain highly conserved elements that may be transcription factor or other regulatory binding sites. We have found two putative ankyrin repeat-containing genes that flank the CFTR gene. Overall sequence analysis suggests conservation of intron/exon boundaries between Fugu and human CFTR and revealed extensive homology between functional protein domains. However, the immediate 5′ regions of human and Fugu CFTR are highly divergent with few conserved sequences apart from those resembling diminished cAMP response elements (CRE) and CAAT box elements. Interestingly, the polymorphic polyT tract located upstream of exon 9 is present in human and Fugu but absent in mouse. Similarly, an intron 1 and intron 9 element common to human and Fugu is absent in mouse. The euryhaline killifish CFTR coding sequence is highly homologous to the Fugu sequence, suggesting that upregulation of CFTR in that species in response to salinity may be regulated transcriptionally.[The sequence data described in this paper have been submitted to the GenBank data library under accession no. , for the combined cosmids 159C9, 146H13, 6M15, and 145M20.]
机译:为了定义控制组织特异性表达的囊性纤维化跨膜调节剂(CFTR)的控制元件,我们已对包括CFTR基因的河豚Fugu rubripes(Fugu)的60 kb基因组DNA进行了测序。 Fugu基因组的这一区域显示出与包含WNT2,CFTR和CBP90基因的人类基因组800 kb序列的同义性。另外,每个基因的基因组结构是保守的。在人,小鼠和Fugu的多序列比对中,推定的WNT2启动子序列显示含有高度保守的元件,该元件可能是转录因子或其他调控结合位点。我们发现两个推定包含锚蛋白重复序列​​的基因位于CFTR基因的侧面。总体序列分析表明,Fugu和人CFTR之间的内含子/外显子边界保守,并揭示了功能蛋白结构域之间的广泛同源性。但是,人类和Fugu CFTR的紧邻5'区域差异很大,除了类似于cAMP响应元件(CRE)和CAAT盒元件减少的保守序列以外,几乎没有保守序列。有趣的是,位于人和Fugu中的外显子9上游的多态性polyT束存在于小鼠中,而缺失。类似地,小鼠和人类中没有常见的内含子1和9内含子元件。淡水幼鱼CFTR编码序列与Fugu序列高度同源,这表明该物种响应盐度而上调的CFTR可能在转录上受到调控。 。 ,对于组合的粘粒159C9、146H13、6M15和145M20。]

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