den Dunnen J T, Moormann R J, Lubsen N H, Schoenmakers J G
Proc Natl Acad Sci U S A. 1986 May;83(9):2855-9. doi: 10.1073/pnas.83.9.2855.
The rat beta B1-crystallin gene is 13.6 kilobases long and contains six exons. The coding region of the gene is divided over five exons. Each functional entity of the protein is encoded by a separate exon except for the carboxyl-terminal extension, which shares the last exon with the fourth protein motif. Exon 2, encoding the amino-terminal extension of the protein, contains two direct repeats with an overall homology of 68% to the rat brain identifier sequence. A copy of the brain identifier sequence is also found in the 3'-flanking region of the gene. The start site of the mRNA was located by S1 nuclease mapping and analysis of the RNA sequence. The 5' end of the gene was shown to be a 27-base-pair noncoding exon, which is separated from the translation start site by 1.36 kilobases of intronic DNA. The 5'-flanking sequence of the beta B1 gene is highly homologous to that of a gamma-crystallin gene.
大鼠βB1-晶体蛋白基因长13.6千碱基,包含6个外显子。该基因的编码区分布在5个外显子上。蛋白质的每个功能实体都由一个单独的外显子编码,但羧基末端延伸部分除外,它与第四个蛋白质基序共享最后一个外显子。编码蛋白质氨基末端延伸部分的外显子2包含两个直接重复序列,与大鼠脑识别序列的总体同源性为68%。在该基因的3'侧翼区域也发现了一个脑识别序列拷贝。通过S1核酸酶图谱分析和RNA序列分析确定了mRNA的起始位点。该基因的5'端是一个27个碱基对的非编码外显子,与翻译起始位点被1.36千碱基的内含子DNA隔开。βB1基因的5'侧翼序列与γ-晶体蛋白基因的高度同源。