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灵长类动物基因组各区域间的突变模式变异

Mutation pattern variation among regions of the primate genome.

作者信息

Casane D, Boissinot S, Chang B H, Shimmin L C, Li W

机构信息

Human Genetics Center, University of Texas Health Science Center, P. O. Box 20334, Houston, TX 77225, USA.

出版信息

J Mol Evol. 1997 Sep;45(3):216-26. doi: 10.1007/pl00006223.

Abstract

We sequenced three argininosuccinate-synthetase-processed pseudogenes (PsiAS-A1, PsiAS-A3, PsiAS-3) and their noncoding flanking sequences in human, orangutan, baboon, and colobus. Our data showed that these pseudogenes were incorporated into the genome of the Old World monkeys after the divergence of the Old World and New World monkey lineages. These pseudogene flanking regions show variable mutation rates and patterns. The variation in the G/C to A/T mutation rate (u) can account for the unequal GC contents at equilibrium: 34.9, 36.9, and 41.7% in the pseudogene PsiAS-A1, PsiAS-A3, and PsiAS-3 flanking regions, respectively. The A/T to G/C mutation rate (v) seems stable and the u/v ratios equal 1.9, 1.7, and 1.4 in the flanking regions of PsiAS-A1, PsiAS-A3, and PsiAS-3, respectively. These "regional" variations of the mutation rate affect the evolution of the pseudogenes, too. The ratio u/v being greater than 1.0 in each case, the overall mutation rate in the GC-rich pseudogenes is, as expected, higher than in their GC-poor flanking regions. Moreover, a "sequence effect" has been found. In the three cases examined u and v are higher (at least 20%) in the pseudogene than in its flanking region-i.e., the pseudogene appears as mutation "hot" spots embedded in "cold" regions. This observation could be partly linked to the fact that the pseudogene flanking regions are long-standing unconstrained DNA sequences, whereas the pseudogenes were relieved of selection on their coding functions only around 30-40 million years ago. We suspect that relatively more mutable sites maintained unchanged during the evolution of the argininosuccinate gene are able to change in the pseudogenes, such sites being eliminated or rare in the flanking regions which have been void of strong selective constraints over a much longer period. Our results shed light on (1) the multiplicity of factors that tune the spontaneous mutation rate and (2) the impact of the genomic position of a sequence on its evolution.

摘要

我们对人、猩猩、狒狒和疣猴中的三个精氨琥珀酸合成酶加工的假基因(PsiAS - A1、PsiAS - A3、PsiAS - 3)及其非编码侧翼序列进行了测序。我们的数据表明,这些假基因是在旧世界猴和新世界猴谱系分化之后整合到旧世界猴的基因组中的。这些假基因侧翼区域显示出可变的突变率和模式。G/C到A/T的突变率(u)的变化可以解释平衡时不等的GC含量:在假基因PsiAS - A1、PsiAS - A3和PsiAS - 3的侧翼区域中,GC含量分别为34.9%、36.9%和41.7%。A/T到G/C的突变率(v)似乎稳定,并且在PsiAS - A1、PsiAS - A3和PsiAS - 3的侧翼区域中,u/v比值分别为1.9、1.7和1.4。这些突变率的“区域”变化也影响着假基因的进化。在每种情况下u/v比值都大于1.0,正如预期的那样,富含GC的假基因中的总体突变率高于其GC含量低的侧翼区域。此外,还发现了一种“序列效应”。在所研究的三种情况下,假基因中的u和v比其侧翼区域更高(至少高20%)——即假基因表现为嵌入在“冷”区域中的突变“热点”。这一观察结果可能部分与以下事实有关:假基因侧翼区域是长期不受约束的DNA序列,而假基因只是在大约3000万到4000万年前才在其编码功能上不再受选择。我们推测,在精氨琥珀酸基因进化过程中相对更多的可变位点在假基因中能够发生变化,这些位点在侧翼区域中被消除或很少见,因为侧翼区域在更长的时间内没有受到强烈的选择约束。我们的结果揭示了(1)调节自发突变率的多种因素,以及(2)序列的基因组位置对其进化的影响。

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