Zhang Yun-Wu, Luo Huai-Rong, Ryder Oliver A, Zhang Ya-Ping
Laboratory of Cellular and Molecular Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, PR China.
Gene. 2004 Aug 18;338(1):47-54. doi: 10.1016/j.gene.2004.05.018.
The upstream regulatory region of the human thymidylate synthase gene (thymidylate synthase enhancer region, TSER) is length polymorphic, attributable to variable numbers of tandemly repeated copies of a 28-bp fragment. It has been found that TSER length polymorphism is correlated to malignancy risk. To further our understanding of the origin and evolution of TSER, this region was investigated among different primates, including hominoids, two subfamilies of the Old World monkeys (OWMs): colobines and cercopithecines, and two species of the New World monkeys (NWMs). In addition to humans, our results show that length polymorphism in TSER is also present in some primate populations, although it appears that this region is length monomorphic in many other primates. We identified three unique repeat motifs in TSER and defined them as R1, R2, and R3, respectively, starting from the 3' end. The same repeat motifs from different species are more similar to each other than different repeat motifs within same species are. Such a paraphyletic pattern suggests that divergence of the three repeat motifs predated divergence of the OWMs/hominoids and the NWMs. The most recent common ancestor (MRCA) of hominoids and the OWMs probably possessed triple repeats but now double and triple repeats are two dominant types in hominoids and the OWMs. In addition, our results show that each of the three repeat motifs may be lost independently. We have also found clues that recombination was involved in formation of tandem repeat polymorphism in TSER.
人类胸苷酸合成酶基因的上游调控区(胸苷酸合成酶增强子区域,TSER)存在长度多态性,这归因于一个28碱基对片段串联重复拷贝数的变化。已发现TSER长度多态性与恶性肿瘤风险相关。为了进一步了解TSER的起源和进化,我们在不同的灵长类动物中对该区域进行了研究,包括类人猿、旧世界猴(OWM)的两个亚科:疣猴亚科和猕猴亚科,以及两种新世界猴(NWM)。除人类外,我们的结果表明,TSER的长度多态性也存在于一些灵长类动物群体中,尽管在许多其他灵长类动物中该区域似乎是长度单态的。我们在TSER中鉴定出三个独特的重复基序,并分别从3'端开始将它们定义为R1、R2和R3。来自不同物种的相同重复基序彼此之间比同一物种内不同的重复基序更相似。这种并系模式表明,这三个重复基序的分化早于旧世界猴/类人猿和新世界猴的分化。类人猿和旧世界猴的最近共同祖先(MRCA)可能拥有三联重复,但现在二联和三联重复是类人猿和旧世界猴中的两种主要类型。此外,我们的结果表明,这三个重复基序中的每一个都可能独立丢失。我们还发现了一些线索,表明重组参与了TSER串联重复多态性的形成。