Begley C G, Robb L, Rockman S, Visvader J, Bockamp E O, Chan Y S, Green A R
Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Gene. 1994 Jan 28;138(1-2):93-9. doi: 10.1016/0378-1119(94)90787-0.
We have determined the molecular structure of the gene encoding the murine SCL protein (helix-loop-helix transcription factor). The gene consists of seven exons spanning approx. 20 kb. The intron/exon structure, coding region sequences and sequences present at the splice junctions were highly conserved between mouse and human. The 5' flanking sequence contains CCAAT and TATA consensus motifs with several putative binding sites for SP-1, AP-1 and GATA-1. Multiple mRNA transcripts were generated by alternate exon usage. The transcripts differed primarily in the 5' untranslated region (UTR), but potentially also encode a smaller SCL protein. Despite the high degree of conservation between species, the heptamer/nonamer signal sequences in the 5' region of the human SCL gene (the frequent site of SCL disruption in human leukemia) were poorly represented in the murine sequence. In keeping with this, structural abnormalities of murine SCL were uncommon in murine leukemias that express the SCL transcript.
我们已经确定了编码小鼠SCL蛋白(螺旋-环-螺旋转录因子)的基因的分子结构。该基因由七个外显子组成,跨度约为20 kb。小鼠和人类之间的内含子/外显子结构、编码区序列以及剪接连接处的序列高度保守。5'侧翼序列包含CCAAT和TATA共有基序,还有几个SP-1、AP-1和GATA-1的假定结合位点。通过外显子的交替使用产生了多种mRNA转录本。这些转录本主要在5'非翻译区(UTR)有所不同,但也可能编码一种较小的SCL蛋白。尽管物种间具有高度保守性,但人类SCL基因5'区域的七聚体/九聚体信号序列(人类白血病中SCL破坏的常见位点)在小鼠序列中表现不佳。与此一致的是,在表达SCL转录本的小鼠白血病中,小鼠SCL的结构异常并不常见。