Suminami Y, Kishi F, Torigoe T, Nakazawa A
Department of Obstetrics and Gynecology, Yamaguchi University School of Medicine.
J Biochem. 1988 Apr;103(4):611-7. doi: 10.1093/oxfordjournals.jbchem.a122315.
The gene encoding cytosolic adenylate kinase (AK1) was isolated from a chicken genomic DNA library by using its cDNA as a hybridization probe. The chicken AK1 gene spanned about 6 kilobase pairs and consisted of 7 exons. Analyses of the 5'-flanking region sequence and S1 nuclease mapping revealed that the transcription initiation site is located at 84 base pairs upstream from the ATG initiation codon. The TATA box and the putative CAT box were located 29 base pairs and 97 base pairs upstream from the transcription initiation site, respectively. A total of 7 GC boxes were found in the 5'-flanking region, the exon 1, and the intron 1. The GC boxes were surrounded by the sequences with extremely high G+C contents. When projected on the three-dimensional structure of the AK1 protein molecule, introns fell either between or near the ends of alpha-helices and beta-strands, and most of the coding exons encoded at least one alpha-helix and one beta-strand. The dot matrix plot analysis between chicken AK1 and bovine mitochondrial adenylate kinase (AK2) suggested that the AK1 gene might have evolved from the AK2 gene by deletion of one or more exon(s).
通过使用其cDNA作为杂交探针,从鸡基因组DNA文库中分离出编码胞质腺苷酸激酶(AK1)的基因。鸡AK1基因跨度约6千碱基对,由7个外显子组成。对5'-侧翼区序列的分析和S1核酸酶图谱分析表明,转录起始位点位于ATG起始密码子上游84个碱基对处。TATA盒和假定的CAT盒分别位于转录起始位点上游29个碱基对和97个碱基对处。在5'-侧翼区、外显子1和内含子1中总共发现了7个GC盒。GC盒被G+C含量极高的序列包围。当投射到AK1蛋白分子的三维结构上时,内含子要么落在α-螺旋和β-链的末端之间,要么靠近其末端,并且大多数编码外显子至少编码一个α-螺旋和一个β-链。鸡AK1和牛线粒体腺苷酸激酶(AK2)之间的点阵图分析表明,AK1基因可能是通过缺失一个或多个外显子而从AK2基因进化而来的。