Miyamoto S, Ohya Y, Ohsumi Y, Anraku Y
Gene. 1987;54(1):125-32. doi: 10.1016/0378-1119(87)90354-4.
The nucleotide sequence of the CLS4 gene controlling Ca2+ regulatory process of bud emergence, which was cloned previously [Ohya et al., J. Bacteriol. 165 (1986) 28-33], was determined. The CLS4 (CDC24) locus encodes a protein consisting of 736 amino acid (aa) residues with an Mr of 83,970. By primer extension mapping, the mRNA start point was located 139 bp upstream from the translation start codon. The predicted CLS4 protein was hydrophilic with two serine + threonine-rich domains in the middle and C-terminal regions. It has two putative Ca2+-binding regions, one being partly homologous to the Ca2+-binding domain of the S-100a protein and the other that of alpha-lactalbumin.
此前已克隆出控制芽萌发Ca²⁺调节过程的CLS4基因[Ohya等人,《细菌学杂志》165(1986)28 - 33],并测定了其核苷酸序列。CLS4(CDC24)基因座编码一种由736个氨基酸残基组成的蛋白质,分子量为83,970。通过引物延伸作图,mRNA起始点位于翻译起始密码子上游139 bp处。预测的CLS4蛋白具有亲水性,在中部和C端区域有两个富含丝氨酸和苏氨酸的结构域。它有两个假定的Ca²⁺结合区域,一个与S - 100a蛋白的Ca²⁺结合结构域部分同源,另一个与α - 乳白蛋白的Ca²⁺结合结构域同源。