首页> 外文期刊>BMC Evolutionary Biology >Phylogenetic analysis of the vertebrate Excitatory/Neutral Amino Acid Transporter (SLC1/EAAT) family reveals lineage specific subfamilies
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Phylogenetic analysis of the vertebrate Excitatory/Neutral Amino Acid Transporter (SLC1/EAAT) family reveals lineage specific subfamilies

机译:脊椎动物兴奋性/中性氨基酸转运蛋白(SLC1 / EAAT)家族的系统发育分析揭示了谱系特定的亚科。

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Background The composition and expression of vertebrate gene families is shaped by species specific gene loss in combination with a number of gene and genome duplication events (R1, R2 in all vertebrates, R3 in teleosts) and depends on the ecological and evolutionary context. In this study we analyzed the evolutionary history of the solute carrier 1 (SLC1) gene family. These genes are supposed to be under strong selective pressure (purifying selection) due to their important role in the timely removal of glutamate at the synapse. Results In a genomic survey where we manually annotated and analyzing sequences from more than 300 SLC1 genes (from more than 40 vertebrate species), we found evidence for an interesting evolutionary history of this gene family. While human and mouse genomes contain 7 SLC1 genes, in prototheria, sauropsida, and amphibia genomes up to 9 and in actinopterygii up to 13 SLC1 genes are present. While some of the additional slc1 genes in ray-finned fishes originated from R3, the increased number of SLC1 genes in prototheria, sauropsida, and amphibia genomes originates from specific genes retained in these lineages. Phylogenetic comparison and microsynteny analyses of the SLC1 genes indicate, that theria genomes evidently lost several SLC1 genes still present in the other lineage. The genes lost in theria group into two new subfamilies of the slc1 gene family which we named slc1a8/eaat6 and slc1a9/eaat7. Conclusions The phylogeny of the SLC1/EAAT gene family demonstrates how multiple genome reorganization and duplication events can influence the number of active genes. Inactivation and preservation of specific SLC1 genes led to the complete loss of two subfamilies in extant theria, while other vertebrates have retained at least one member of two newly identified SLC1 subfamilies.
机译:背景脊椎动物基因家族的组成和表达受物种特异性基因缺失以及许多基因和基因组复制事件(所有脊椎动物中的R1,R2,硬骨鱼类中的R3)的影响而定,并取决于生态和进化环境。在这项研究中,我们分析了溶质载体1(SLC1)基因家族的进化历史。这些基因由于在及时清除突触中的谷氨酸中起重要作用,因此被认为具有强大的选择压力(纯化选择)。结果在一项基因组调查中,我们手动注释和分析了300多个SLC1基因(来自40多个脊椎动物)的序列,我们发现了该基因家族有趣的进化史的证据。人和小鼠的基因组包含7个SLC1基因,而在Prototheria,sauropsida和两栖动物中,基因组最多可以包含9个,放线翅目中最多可以包含13个SLC1基因。虽然有鳍鱼类中的一些其他slc1基因起源于R3,但原色,蜥脚目和两栖动物基因组中SLC1基因数量的增加却来自保留在这些谱系中的特定基因。 SLC1基因的系统发育比较和微同义分析表明,Theria基因组显然丢失了仍然存在于其他谱系中的几个SLC1基因。在theria组中丢失的基因分为slc1基因家族的两个新亚家族,我们将其命名为slc1a8 / eaat6和slc1a9 / eaat7。结论SLC1 / EAAT基因家族的系统发育证明了多重基因组重组和复制事件如何影响活性基因的数量。特定SLC1基因的失活和保存导致现存肿瘤中两个亚科的完全丧失,而其他脊椎动物则保留了两个新发现的SLC1亚科中的至少一个成员。

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