Reue K, Leete T H
Wadsworth VA Medical Center, Los Angeles, California 90073.
J Biol Chem. 1991 Jul 5;266(19):12715-21.
We have detected three unique apolipoprotein A-IV (apoA-IV) charge isoforms in strains of commensal mice. The cDNA sequences for one representative of each isoform (Mus domestesticus strains C57BL/6J and 129/J and Mus castaneus) revealed a polymorphism within a series of four imperfect repeats encoding the sequence Glu-Gln-Ala/Val-Gln. Insertions or deletions of 12 nucleotides within this repetitive region have given rise to three genotypes characterized by three (129), four (C57BL/6), or five (M. castaneus) copies of the repeat unit. To ascertain the extent of this variation among other species of the Mus genus, we sequenced this region of apoA-IV cDNAs from eight additional M. domesticus inbred strains and from five wild-derived Mus species. All eight additional M. domesticus strains examined had four repeat units, as found in C57BL/6. Among wild-derived mice, however, one species (Mus spretus) had three repeats, two species (Mus cookii and Mus cervicolor) had four repeats, and two species (Mus hortulanus and Mus minutoides) had five repeats. A lack of correlation between the number of repeat units and the phylogeny of Mus species indicates that independent mutations may have occurred throughout the evolution of specific mouse lineages. We suggest that the repetitive nature of the polymorphic sequence may predispose this region to slippage errors during DNA replication, resulting in frequent deletion/insertion mutations.
我们在共生小鼠品系中检测到三种独特的载脂蛋白A-IV(apoA-IV)电荷异构体。每种异构体的一个代表(小家鼠品系C57BL/6J和129/J以及栗色小鼠)的cDNA序列显示,在编码Glu-Gln-Ala/Val-Gln序列的一系列四个不完全重复序列中存在多态性。该重复区域内12个核苷酸的插入或缺失产生了三种基因型,其特征分别为重复单元的三个(129)、四个(C57BL/6)或五个(栗色小鼠)拷贝。为了确定小家鼠属其他物种之间这种变异的程度,我们对另外八个小家鼠近交系和五个野生小家鼠物种的apoA-IV cDNA的该区域进行了测序。所有检测的另外八个小家鼠品系都有四个重复单元,如在C57BL/6中发现的那样。然而,在野生小家鼠中,一个物种(西班牙小鼠)有三个重复序列,两个物种(库克氏小鼠和黄颈小鼠)有四个重复序列,两个物种(园圃小鼠和细小鼠)有五个重复序列。重复单元数量与小家鼠物种系统发育之间缺乏相关性,这表明在特定小鼠谱系的整个进化过程中可能发生了独立的突变。我们认为,多态性序列的重复性质可能使该区域在DNA复制过程中易发生滑动错误,从而导致频繁的缺失/插入突变。