Zhu T, Schupp J M, Oliphant A, Keim P
Department of Biological Sciences, Northern Arizona University, Flagstaff 86011.
Mol Gen Genet. 1994 Sep 28;244(6):638-45. doi: 10.1007/BF00282754.
Soybean is believed to be a diploidized tetraploid generated from an allotetraploid ancestor. In this study, we used hypomethylated genomic DNA as a source of probes to investigate the genomic structure and methylation patterns of duplicated sequences. Forty-five genomic clones from Phaseolus vulgaris and 664 genomic clones from Glycine max were used to examine the duplicated regions in the soybean genome. Southern analysis of genomic DNA using probes from both sources revealed that greater than 15% of the hypomethylated genomic regions were only present once in the soybean genome. The remaining ca. 85% of the hypomethylated regions comprise duplicated or middle repetitive DNA sequences. If only the ratio of single to duplicate probe patterns is considered, it appears that 25% of the single-copy sequences have been lost. By using a subset of probes that only detected duplicated sequences, we examined the methylation status of the homeologous genomes with the restriction enzymes MspI and HpaII. We found that in all cases both copies of these regions were hypomethylated, although there were examples of low-level methylation. It appears that duplicate sequences are being eliminated in the diploidization process. Our data reveal no evidence that duplicated sequences are being "silenced" by inactivation correlated with methylation patterns.
大豆被认为是由异源四倍体祖先产生的二倍体化四倍体。在本研究中,我们使用低甲基化基因组DNA作为探针来源,以研究重复序列的基因组结构和甲基化模式。使用来自菜豆的45个基因组克隆和来自大豆的664个基因组克隆来检测大豆基因组中的重复区域。使用来自这两个来源的探针对基因组DNA进行Southern分析表明,超过15%的低甲基化基因组区域在大豆基因组中仅出现一次。其余约85%的低甲基化区域包含重复或中度重复的DNA序列。如果仅考虑单拷贝与重复探针模式的比例,似乎25%的单拷贝序列已经丢失。通过使用仅检测重复序列的探针子集,我们用限制性内切酶MspI和HpaII检测了同源基因组的甲基化状态。我们发现,在所有情况下,这些区域的两个拷贝都是低甲基化的,尽管存在低水平甲基化的例子。在二倍体化过程中,重复序列似乎正在被消除。我们的数据没有显示出重复序列因与甲基化模式相关的失活而被“沉默”的证据。