Marine Biodiversity Research Program, Japan Agency for Marine-Earth Science and Technology, Natsushima-cho, Yokosuka, Kanagawa 237-0061, Japan.
BMC Evol Biol. 2011 Oct 3;11:285. doi: 10.1186/1471-2148-11-285.
Two Calyptogena clam intracellular obligate symbionts, Ca. Vesicomyosocius okutanii (Vok; C. okutanii symbiont) and Ca. Ruthia magnifica (Rma; C. magnifica symbiont), have small genomes (1.02 and 1.16 Mb, respectively) with low G+C contents (31.6% and 34.0%, respectively) and are thought to be in an ongoing stage of reductive genome evolution (RGE). They lack recA and some genes for DNA repair, including mutY. The loss of recA and mutY is thought to contribute to the stabilization of their genome architectures and GC bias, respectively. To understand how these genes were lost from the symbiont genomes, we surveyed these genes in the genomes from 10 other Calyptogena clam symbionts using the polymerase chain reaction (PCR).
Phylogenetic trees reconstructed using concatenated 16S and 23S rRNA gene sequences showed that the symbionts formed two clades, clade I (symbionts of C. kawamurai, C. laubieri, C. kilmeri, C. okutanii and C. soyoae) and clade II (those of C. pacifica, C. fausta, C. nautilei, C. stearnsii, C. magnifica, C. fossajaponica and C. phaseoliformis). recA was detected by PCR with consensus primers for recA in the symbiont of C. phaseoliformis. A detailed homology search revealed a remnant recA in the Rma genome. Using PCR with a newly designed primer set, intact recA or its remnant was detected in clade II symbionts. In clade I symbionts, the recA coding region was found to be mostly deleted.In the Rma genome, a pseudogene of mutY was found. Using PCR with newly designed primer sets, mutY was not found in clade I symbionts but was found in clade II symbionts. The G+C content of 16S and 23S rRNA genes in symbionts lacking mutY was significantly lower than in those with mutY.
The extant Calyptogena clam symbionts in clade II were shown to have recA and mutY or their remnants, while those in clade I did not. The present results indicate that the extant symbionts are losing these genes in RGE, and that the loss of mutY contributed to the GC bias of the genomes during their evolution.
两种蛤蛎体内必需共生的拟杆菌属细菌,Ca. Vesicomyosocius okutanii(Vok;C. okutanii 共生菌)和 Ca. Ruthia magnifica(Rma;C. magnifica 共生菌),基因组较小(分别为 1.02 和 1.16 Mb),GC 含量低(分别为 31.6%和 34.0%),且被认为处于还原基因组进化(RGE)的进行阶段。它们缺乏 recA 和一些 DNA 修复基因,包括 mutY。recA 和 mutY 的缺失被认为分别有助于稳定它们的基因组结构和 GC 偏倚。为了了解这些基因是如何从共生菌基因组中丢失的,我们使用聚合酶链反应(PCR)在其他 10 种蛤蛎共生菌的基因组中对这些基因进行了调查。
使用 16S 和 23S rRNA 基因序列的系统发育树重建表明,共生菌形成了两个分支,分支 I(C. kawamurai、C. laubieri、C. kilmeri、C. okutanii 和 C. soyoae 的共生菌)和分支 II(C. pacifica、C. fausta、C. nautilei、C. stearnsii、C. magnifica、C. fossajaponica 和 C. phaseoliformis 的共生菌)。在 C. phaseoliformis 共生菌中使用 recA 共识引物的 PCR 检测到了 recA。详细的同源搜索显示,在 Rma 基因组中存在 recA 的残余物。使用新设计的引物对的 PCR 检测到分支 II 共生菌中完整的 recA 或其残余物。在分支 I 共生菌中,recA 编码区大部分缺失。在 Rma 基因组中,发现了 mutY 的假基因。使用新设计的引物对的 PCR 检测到分支 I 共生菌中没有 mutY,但在分支 II 共生菌中发现了 mutY。缺乏 mutY 的共生菌 16S 和 23S rRNA 基因的 G+C 含量明显低于具有 mutY 的共生菌。
本研究表明,分支 II 中现存的蛤蛎共生菌具有 recA 和 mutY 或其残余物,而分支 I 中的共生菌则没有。本研究结果表明,现存的共生菌正在 RGE 中失去这些基因,而 mutY 的缺失有助于它们在进化过程中基因组的 GC 偏倚。