Pogozelski Wendy K, Fletcher Leah D, Cassar Carolyn A, Dunn David A, Trounce Ian A, Pinkert Carl A
Department of Chemistry, State University of New York at Geneseo, Geneseo, NY 14454, USA.
Gene. 2008 Jul 15;418(1-2):27-33. doi: 10.1016/j.gene.2008.04.001. Epub 2008 Apr 10.
Knowledge of the mitochondrial DNA (mtDNA) sequence of divergent murine species is critical from both a phylogenetic perspective and in understanding nuclear-mitochondrial interactions, particularly as the latter influences our xenocybrid models of mitochondrial disease. To this end, the sequence of the mitochondrial genome of the murine species Mus terricolor (formerly Mus dunni) is reported and compared with the published sequence for the common laboratory mouse Mus musculus domesticus strain C57BL/6J. These species are of interest because xenomitochondrial cybrid mice were created that harbor M. terricolor mtDNA in a M. m. domesticus nuclear background. Although the total of 1763 nucleotide substitutions represents striking heterogeneity, the majority of these are silent, leading to highly conserved protein sequences with only 159 amino acid differences. Moreover, 58% of these amino acid differences represented conservative substitutions. All of the tRNA genes and rRNA genes have homology of 91% or greater. The control region shows the greatest heterogeneity, as expected, with 85% homology overall. Regions of 100% homology were found for Conserved Sequence Block I, Conserved Sequence Block III and the L-strand origin of replication. Complex I genes showed the greatest degree of difference among protein-coding genes with amino acid homology of 91-97% among the seven mitochondrial genes. Complexes III and IV genes show high homology ranging from 98-100%. From these data, complex I differences appear most critical for the viability of M. m. domesticus: M. terricolor cybrids. Moreover, the sequence information reported here should be useful in identifying critical regions for mitochondrial transfer between species, for furthering the understanding of mitochondrial dynamics and pathology in transmitochondrial organisms, and for the study of Mus genus origins.
了解不同鼠类物种的线粒体DNA(mtDNA)序列,从系统发育的角度以及理解核-线粒体相互作用方面都至关重要,特别是当后者影响我们的线粒体疾病异种杂交模型时。为此,本文报道了鼠类物种丛林小鼠(原称邓氏小鼠)的线粒体基因组序列,并将其与已发表的普通实验小鼠小家鼠C57BL/6J品系的序列进行比较。这些物种之所以受到关注,是因为创建了在小家鼠核背景中携带丛林小鼠mtDNA的异种线粒体杂交小鼠。尽管总共1763个核苷酸替换代表了显著的异质性,但其中大多数是沉默替换,导致蛋白质序列高度保守,仅有159个氨基酸差异。此外,这些氨基酸差异中有58%是保守替换。所有的tRNA基因和rRNA基因都具有91%或更高的同源性。正如预期的那样,控制区显示出最大的异质性,总体同源性为85%。在保守序列块I、保守序列块III和L链复制起点发现了100%同源的区域。在七个线粒体基因中,复合体I基因在蛋白质编码基因中显示出最大程度的差异,氨基酸同源性为91%-97%。复合体III和IV基因显示出98%-100%的高同源性。从这些数据来看,复合体I的差异似乎对小家鼠-丛林小鼠杂交体的存活最为关键。此外,本文报道的序列信息在识别物种间线粒体转移的关键区域、深化对线粒体生物中动力学和病理学的理解以及研究鼠属起源方面应该是有用的。