Reichman Jay R, Vize Peter D
US Environmental Protection Agency, Western Ecology Division, Corvallis, Oregon, United States of America; Oregon State University, Department of Botany and Plant Pathology, Corvallis, Oregon, United States of America.
University of Calgary, Department of Biological Sciences, Calgary, Alberta, Canada.
PLoS One. 2014 Oct 17;9(10):e110608. doi: 10.1371/journal.pone.0110608. eCollection 2014.
Here we document introns in two Symbiodinium clades that were most likely gained following divergence of this genus from other peridinin-containing dinoflagellate lineages. Soluble peridinin-chlorophyll a-proteins (sPCP) occur in short and long forms in different species. Duplication and fusion of short sPCP genes produced long sPCP genes. All short and long sPCP genes characterized to date, including those from free living species and Symbiodinium sp. 203 (clade C/type C2) are intronless. However, we observed that long sPCP genes from two Caribbean Symbiodinium clade B isolates each contained two introns. To test the hypothesis that introns were gained during radiation of clade B, we compared sPCP genomic and cDNA sequences from 13 additional distinct Caribbean and Pacific Symbiodinium clade A, B, and F isolates. Long sPCP genes from all clade B/B1 and B/B19 descendants contain orthologs of both introns. Short sPCP genes from S. pilosum (A/A2) and S. muscatinei (B/B4) plus long sPCP genes from S. microadriaticum (A/A1) and S. kawagutii (F/F1) are intronless. Short sPCP genes of S. microadriaticum have a third unique intron. Symbiodinium clade B long sPCP sequences are useful for assessing divergence among B1 and B19 descendants. Phylogenetic analyses of coding sequences from four dinoflagellate orders indicate that introns were gained independently during radiation of Symbiodinium clades A and B. Long sPCP introns were present in the most recent common ancestor of Symbiodinium clade B core types B1 and B19, which apparently diverged sometime during the Miocene. The clade A short sPCP intron was either gained by S. microadriaticum or possibly by the ancestor of Symbiodinium types A/A1, A3, A4 and A5. The timing of short sPCP intron gain in Symbiodinium clade A is less certain. But, all sPCP introns were gained after fusion of ancestral short sPCP genes, which we confirm as occurring once in dinoflagellate evolution.
在此,我们记录了共生藻两个分支中的内含子,这些内含子很可能是在该属与其他含多甲藻素的甲藻谱系分化之后获得的。可溶性多甲藻素 - 叶绿素a - 蛋白(sPCP)在不同物种中以短形式和长形式存在。短sPCP基因的复制和融合产生了长sPCP基因。迄今为止所表征的所有短sPCP基因和长sPCP基因,包括来自自由生活物种和共生藻203株(C分支/C2型)的基因,均无内含子。然而,我们观察到来自两个加勒比共生藻B分支分离株的长sPCP基因各自含有两个内含子。为了检验内含子是在B分支辐射期间获得的这一假设,我们比较了另外13个来自加勒比和太平洋的不同共生藻A、B和F分支分离株的sPCP基因组序列和cDNA序列。所有B/B1和B/B19后代的长sPCP基因都包含这两个内含子的直系同源物。来自多毛共生藻(A/A2)和马斯卡廷共生藻(B/B4)的短sPCP基因,以及来自微小亚得里亚海共生藻(A/A1)和川口共生藻(F/F1)的长sPCP基因均无内含子。微小亚得里亚海共生藻的短sPCP基因有第三个独特的内含子。共生藻B分支的长sPCP序列有助于评估B1和B19后代之间的差异。对四个甲藻目编码序列的系统发育分析表明,内含子是在共生藻A和B分支辐射期间独立获得的。长sPCP内含子存在于共生藻B分支核心类型B1和B19的最近共同祖先中,它们显然在中新世的某个时期分化。A分支短sPCP内含子要么是由微小亚得里亚海共生藻获得的,要么可能是由共生藻A/A1、A3、A4和A5类型的祖先获得的。共生藻A分支中短sPCP内含子获得的时间不太确定。但是,所有sPCP内含子都是在祖先短sPCP基因融合之后获得的,我们确认这种融合在甲藻进化过程中只发生过一次。