Dept. of Human Genetics, University of Utah Health Sciences Center, Salt Lake City, Utah 84112, USA.
BMC Genomics. 2009 Nov 16;10:530. doi: 10.1186/1471-2164-10-530.
Recombination rates vary widely across the human genome, but little of that variation is correlated with known DNA sequence features. The genome contains more than one million Alu mobile element insertions, and these insertions have been implicated in non-homologous recombination, modulation of DNA methylation, and transcriptional regulation. If individual Alu insertions have even modest effects on local recombination rates, they could collectively have a significant impact on the pattern of linkage disequilibrium in the human genome and on the evolution of the Alu family itself.
We carried out sequencing, SNP identification, and SNP genotyping around 19 AluY insertion loci in 347 individuals sampled from diverse populations, then used the SNP genotypes to estimate local recombination rates around the AluY loci. The loci and SNPs were chosen so as to minimize other factors (such as SNP ascertainment bias and SNP density) that could influence recombination rate estimates. We detected a significant increase in recombination rate within approximately 2 kb of the AluY insertions in our African population sample. To test this observation against a larger set of AluY insertions, we applied our locus- and SNP-selection design and analyses to the HapMap Phase II data. In that data set, we observed a significantly increased recombination rate near AluY insertions in both the CEU and YRI populations.
We show that the presence of a fixed AluY insertion is significantly predictive of an elevated local recombination rate within 2 kb of the insertion, independent of other known predictors. The magnitude of this effect, approximately a 6% increase, is comparable to the effects of some recombinogenic DNA sequence motifs identified via their association with recombination hot spots.
人类基因组中的重组率差异很大,但这些差异与已知的 DNA 序列特征几乎没有相关性。基因组中含有超过 100 万个 Alu 移动元件插入,这些插入物与非同源重组、DNA 甲基化的调节和转录调控有关。如果单个 Alu 插入物对局部重组率有一定的影响,那么它们可能会对人类基因组中连锁不平衡的模式以及 Alu 家族本身的进化产生重大影响。
我们在来自不同人群的 347 个人中,对 19 个 AluY 插入位点进行了测序、SNP 鉴定和 SNP 基因分型,然后利用 SNP 基因型来估计 AluY 位点周围的局部重组率。选择这些位点和 SNPs 是为了尽量减少其他可能影响重组率估计的因素(如 SNP 确定偏差和 SNP 密度)。我们在非洲人群样本中检测到 AluY 插入附近的重组率显著增加。为了在更大的 AluY 插入组中验证这一观察结果,我们将我们的位点和 SNP 选择设计和分析应用于 HapMap Phase II 数据。在该数据集,我们观察到 CEU 和 YRI 人群中 AluY 插入附近的重组率显著增加。
我们表明,固定的 AluY 插入的存在与插入附近 2kb 内的升高的局部重组率显著相关,独立于其他已知的预测因子。这种效应的幅度约为 6%,与通过与重组热点相关联而确定的一些重组性 DNA 序列基序的效应相当。