Hyman Bradley C, Lewis Samantha C, Tang Sha, Wu Zhen
Department of Biology, University of California, Riverside, CA 92521, USA.
Genetica. 2011 May;139(5):611-5. doi: 10.1007/s10709-010-9531-3. Epub 2010 Dec 7.
Rare syntenic conservation, sequence duplication, and the use of both DNA strands to encode genes are signature architectural features defining mitochondrial genomes of enoplean nematodes. These characteristics stand in contrast to the more conserved mitochondrial genome sizes and transcriptional organizations of mitochondrial DNAs (mtDNAs) derived from chromadorean nematodes. To address the frequency of gene rearrangement within nematode mitochondrial DNA (mtDNA), mitochondrial genome variation has been characterized within a more confined enoplean taxonomic unit, the family Mermithidae. The complete nucleotide sequences of the mosquito parasitic nematodes Romanomermis culicivorax, R. nielseni, and R. iyengari mtDNA have been determined. Duplicated expanses encompassing different regions of the mitochondrial genomes were found in each of these congeners. These mtDNA shared few rRNA and protein gene junctions, indicating extensive gene rearrangement within the Romanomermis lineage. Rapid structural changes are also observed at the conspecific level where no two individual nematodes carry the same haplotype. Rolling circle amplification was used to isolate complete mitochondrial genomes from individuals in local populations of Thaumamermis cosgrovei, a parasite of terrestrial isopods. Mitochondrial DNA length variants ranging from 19 to 34 kb are observed, but haplotypes are not shared between any two individuals. The complete nucleotide sequences of three haplotypes have been determined, revealing a constant region encoding most mitochondrial genes and a hypervariable segment that contains intact and pseudogene copies of several mitochondrial genes, duplicated to different copy numbers, resulting in mtDNA size variation. Constant rearrangement generates new T. cosgrovei mtDNA forms.
罕见的共线性保守、序列重复以及利用两条DNA链编码基因是界定内寄生线虫线粒体基因组的标志性结构特征。这些特征与来自色矛线虫的线粒体DNA(mtDNA)更保守的线粒体基因组大小和转录组织形成对比。为了研究线虫线粒体DNA(mtDNA)内基因重排的频率,已在一个更受限的内寄生线虫分类单元——索线虫科中对线粒体基因组变异进行了表征。已确定了寄生在蚊子体内的线虫库蚊罗索线虫、尼尔森罗索线虫和伊氏罗索线虫mtDNA的完整核苷酸序列。在这些同属线虫的每一种中都发现了包含线粒体基因组不同区域的重复区域。这些mtDNA很少有rRNA和蛋白质基因连接点,表明罗索线虫谱系内存在广泛的基因重排。在同种水平上也观察到快速的结构变化,没有两条线虫个体携带相同的单倍型。滚环扩增被用于从陆地等足类寄生虫科斯格罗夫索马线虫当地种群的个体中分离完整的线粒体基因组。观察到线粒体DNA长度变异范围为19至34 kb,但任意两个个体之间都不共享单倍型。已确定了三种单倍型的完整核苷酸序列,揭示了一个编码大多数线粒体基因的恒定区域和一个高变片段,该片段包含几个线粒体基因的完整和假基因拷贝,以不同的拷贝数重复,导致mtDNA大小变异。持续的重排产生了新的科斯格罗夫索马线虫mtDNA形式。