Roper M D, Straubhaar J R, Kraus E, Sokolová J, Hrebícek M, Kraus J P
Department of Pediatrics, C233, University of Colorado School of Medicine, 4200 E. Ninth Avenue, Denver, Colorado 80262, USA.
Mamm Genome. 1996 Oct;7(10):754-7. doi: 10.1007/s003359900226.
We have isolated and characterized a genomic fragment encompassing the first six exons and 2.6 kbp 5' flanking sequence of the rat cystathionine beta-synthase (CBS) gene. A previously unknown exon approximately 3 kbp upstream of exon 1 was identified. The transcription start site was mapped to approximately 3 kbp upstream from the translation start codon and contains a consensus cap signal. The putative promoter region contains three GC boxes, in both orientations, and no TATA box. We have also compared a 1171-bp-long DNA sequence of the 5' end of the rat CBS gene with the homologous mouse region of 1125 bp. We found two homologous Sp1 sites in the mouse gene and an overall sequence conservation of 70% with 88-89% similarity in the 80-bp regions surrounding the intron 0 splice sites.
我们分离并鉴定了一个基因组片段,该片段包含大鼠胱硫醚β-合酶(CBS)基因的前六个外显子和2.6千碱基对的5'侧翼序列。在第1外显子上游约3千碱基处鉴定出一个先前未知的外显子。转录起始位点定位于翻译起始密码子上游约3千碱基处,并包含一个共有帽信号。推测的启动子区域包含三个GC盒,呈两种方向排列,且无TATA盒。我们还将大鼠CBS基因5'端1171碱基对长的DNA序列与小鼠同源的1125碱基对区域进行了比较。我们在小鼠基因中发现了两个同源的Sp1位点,并且在第0内含子剪接位点周围80碱基对区域的总体序列保守性为70%,相似性为88 - 89%。