Lluisma A O, Ragan M A
Institute for Marine Biosciences, National Research Council of Canada, and Department of Biology, Dalhousie University, Halifax, NS, Canada B3H 4J1.
Curr Genet. 1998 Aug;34(2):105-11. doi: 10.1007/s002940050373.
The biosynthesis of starch in red algae occurs in the cytosol, in contrast to green plants where it takes place in the plastid. We have cloned a nuclear gene from the red alga Gracilaria gracilis that encodes a homolog of starch-branching enzymes (SBEs); this gene, which is apparently intron-free, was designated as GgSBE1. A potential TATA box, CAAT boxes, and other potential regulatory elements were observed in its 5' flanking region. The encoded 766-aa peptide shares significant sequence similarity with SBEs from green plants (at least 40%), and with glycogen-branching enzymes (GBEs) from human (46%) and Saccharomyces cerevisiae (45%). Southern-hybridization analysis indicates that the gene is single-copy, although weaker signals suggest that related genes exist in the genome of G. gracilis. Phylogenetic analyses indicate that GgSBE1 groups within the eukaryote branching enzymes (BEs) and not with eubacterial GBEs, suggesting that its gene has not been derived directly from an endosymbiotic cyanobacterium, but instead is ancestrally eukaryotic.
与淀粉合成发生在质体中的绿色植物不同,红藻中的淀粉生物合成发生在细胞质中。我们从红藻龙须菜中克隆了一个核基因,该基因编码淀粉分支酶(SBEs)的一个同源物;这个基因显然没有内含子,被命名为GgSBE1。在其5'侧翼区域观察到一个潜在的TATA框、CAAT框和其他潜在的调控元件。编码的766个氨基酸的肽与绿色植物的SBEs(至少40%)、人类的糖原分支酶(GBEs)(46%)和酿酒酵母的GBEs(45%)具有显著的序列相似性。Southern杂交分析表明该基因是单拷贝的,尽管较弱的信号表明龙须菜基因组中存在相关基因。系统发育分析表明,GgSBE1属于真核生物分支酶(BEs)类群,而不是与真细菌GBEs在一起,这表明其基因并非直接来源于内共生蓝细菌,而是在进化上起源于真核生物。