van der Kuyl A C, Kuiken C L, Dekker J T, Perizonius W R, Goudsmit J
Human Retrovirus Laboratory, Academic Medical Centre, Amsterdam, The Netherlands.
J Mol Evol. 1995 Jun;40(6):652-7. doi: 10.1007/BF00160513.
Monkey mummy bones and teeth originating from the North Saqqara Baboon Galleries (Egypt), soft tissue from a mummified baboon in a museum collection, and nineteenth/twentieth-century skin fragments from mangabeys were used for DNA extraction and PCR amplification of part of the mitochondrial 12S rRNA gene. Sequences aligning with the 12S rRNA gene were recovered but were only distantly related to contemporary monkey mitochondrial 12S rRNA sequences. However, many of these sequences were identical or closely related to human nuclear DNA sequences resembling mitochondrial 12S rRNA (isolated from a cell line depleted in mitochondria) and therefore have to be considered contamination. Subsequently in a separate study we were able to recover genuine mitochondrial 12S rRNA sequences from many extant species of nonhuman Old World primates and sequences closely resembling the human nuclear integrations. Analysis of all sequences by the neighbor-joining (NJ) method indicated that mitochondrial DNA sequences and their nuclear counterparts can be divided into two distinct clusters. One cluster contained all temporary cytoplasmic mitochondrial DNA sequences and approximately half of the monkey nuclear mitochondriallike sequences. A second cluster contained most human nuclear sequences and the other half of monkey nuclear sequences with a separate branch leading to human and gorilla mitochondrial and nuclear sequences. Sequences recovered from ancient materials were equally divided between the two clusters. These results constitute a warning for when working with ancient DNA or performing phylogenetic analysis using mitochondrial DNA as a target sequence: Nuclear counterparts of mitochondrial genes may lead to faulty interpretation of results.
来自北萨卡拉狒狒画廊(埃及)的猴木乃伊骨骼和牙齿、博物馆收藏的一只木乃伊化狒狒的软组织以及19世纪/20世纪白眉猴的皮肤碎片被用于DNA提取和线粒体12S rRNA基因部分片段的PCR扩增。回收了与12S rRNA基因比对的序列,但它们与当代猴线粒体12S rRNA序列的关系很遥远。然而,这些序列中有许多与类似线粒体12S rRNA的人类核DNA序列相同或密切相关(从线粒体缺失的细胞系中分离),因此必须被视为污染。随后在另一项研究中,我们能够从许多现存的旧世界非人灵长类物种中回收真正的线粒体12S rRNA序列以及与人类核整合序列非常相似的序列。通过邻接法(NJ)对所有序列进行分析表明,线粒体DNA序列及其核对应物可分为两个不同的簇。一个簇包含所有临时细胞质线粒体DNA序列和大约一半的猴核线粒体样序列。第二个簇包含大多数人类核序列和另一半猴核序列,有一个单独的分支通向人类和大猩猩的线粒体及核序列。从古代材料中回收的序列在两个簇之间平均分配。这些结果为处理古代DNA或使用线粒体DNA作为目标序列进行系统发育分析时提供了一个警示:线粒体基因的核对应物可能导致对结果的错误解读。