Yao C W, Leu J H, Chin C, Chou C K, Huang C J
Graduate Institute of Life Science, National Defense Medical Center, Taipei, Taiwan.
DNA Cell Biol. 1998 Jan;17(1):69-82. doi: 10.1089/dna.1998.17.69.
The round-spotted pufferfish Tetraodon fluviatilis has a genome size of 380 Mb which is slightly smaller than that of another pufferfish Fugu rubripes rubripes (Fugu). Due to its compact genome and small introns, Fugu has been introduced as a model for genome studies. Recently, the round-spotted pufferfish has also been proposed as a new model for genome studies because of the ease in obtaining material and high-sequence homology to that of Fugu. In this study, we have cloned and characterized the snf5 and set genes from the round-spotted pufferfish. The snf5 gene is composed of 9 exons spanning about 2.9 kb whereas the set gene consists of 8 exons spanning about 2.7 kb. They are linked in a tail-to-tail manner with an intergenic region of about 6.5 kb. So far, the genomic structures of human snf5 and set genes are unknown. Based on our data, the pufferfish SNF5 and SET display high amino acid sequence identity (>90%) with the respective human genes. By primer extension and sequence analysis, we found that putative promoter region of the snf5 gene contains a typical TATA box and numerous potential binding sites for transcription factors including AP1, AP2, AP3, c-Myb, HNF-5, and NF-IL6. As for the set gene, its promoter region does not have any TATA or CCAAT motif and contains a few potential binding sites for transcriptional factors such as c-Myb and gamma-IRE. When these promoter regions were placed upstream of the CAT reporter gene and transfected into a carp CF cell line, the 5'-upstream 1.6-kb DNA fragment of the snf5 gene displayed stronger promoter activity, approximately three-fold higher than that of the 5'-upstream 1.3 kb DNA fragment of the set gene. By transient expression and immunofluorescent staining, we also showed that the pufferfish SNF5 and SET are nuclear proteins, consistent with their postulated roles as transcriptional factors.
圆点河豚(Tetraodon fluviatilis)的基因组大小为380兆碱基,略小于另一种河豚红鳍东方鲀(Fugu rubripes rubripes,简称Fugu)。由于其基因组紧凑且内含子小,Fugu已被引入作为基因组研究的模型。最近,圆点河豚也因其材料获取容易且与Fugu具有高度序列同源性而被提议作为基因组研究的新模型。在本研究中,我们从圆点河豚中克隆并鉴定了snf5和set基因。snf5基因由9个外显子组成,跨度约2.9千碱基,而set基因由8个外显子组成,跨度约为2.7千碱基。它们以尾对尾的方式相连,基因间隔区约为6.5千碱基。到目前为止,人类snf5和set基因的基因组结构尚不清楚。根据我们的数据,河豚的SNF5和SET与相应的人类基因显示出高氨基酸序列同一性(>90%)。通过引物延伸和序列分析,我们发现snf5基因的假定启动子区域包含一个典型的TATA盒以及许多潜在的转录因子结合位点,包括AP1、AP2、AP3、c-Myb、HNF-5和NF-IL6。至于set基因,其启动子区域没有任何TATA或CCAAT基序,并且包含一些转录因子的潜在结合位点,如c-Myb和γ-IRE。当这些启动子区域置于CAT报告基因上游并转染到鲤鱼CF细胞系中时,snf5基因的5'上游1.6千碱基DNA片段显示出更强的启动子活性,比set基因的5'上游1.3千碱基DNA片段高约三倍。通过瞬时表达和免疫荧光染色,我们还表明河豚的SNF5和SET是核蛋白,这与其作为转录因子的假定作用一致。