Dipartimento di Biologia delle Piante Agrarie della Università, Sezione di Genetica, Via G. Matteotti 1/B, I-56124, Pisa, Italy.
Theor Appl Genet. 1996 Mar;92(3-4):285-91. doi: 10.1007/BF00223670.
Complex alterations in the redundancy and methylation of repeated DNA sequences were shown to differentiate the nuclear genome of individuals belonging to single progenies of homozygous plants of the sunflower. DNA was extracted from seedlings obtained from seeds collected at the periphery of flowering heads (P DNA) or from seedlings obtained from seeds collected in their middle (M DNA). Three fractions of repeated sequences were isolated from genomic DNA: a highly repetitive fraction (HR), which reassociates within an equivalent Cot of about 2 × 10(-1), and two medium repetitive fractions (MR1 and MR2) having Cot ranges of about 2 × 10(-1)-2 and 2-10(2), respectively. Denaturation kinetics allowed different sequence families to be recognized within each fraction of repetitive DNA, and showed significant differences in sequence redundancy to occur between P and M DNA, particularly as far as the MR2 fraction is concerned. Most DNA sequence families are more represented in P DNA than in M DNA. However, the redundancy of certain sequences is greater in the latter than in the former. Each repetitive DNA fraction was hybridized to Southern blots of genomic P or M DNA which was digested to completion by three pairs of isoschizomeric restriction endonucleases which are either insensitive or sensitive to the methylation of a cytosine in the recognition site. The results obtained showed that the repetitive DNA of H. annuus is highly methylated. Clear-cut differences in the degree of methylation of P and M DNA were found, and these differences were particularly apparent in the MR2 fraction. It is suggested that alterations in the redundancy of given DNA sequences and changes in their methylation patterns are complementary ways to produce continuous genotypic variability within the species which can be exploited in environmental adaptation.
向日葵单株纯合自交系后代个体的核基因组中,重复 DNA 序列的重复和甲基化发生复杂改变,可将其区分开来。从开花头部边缘收集的种子获得的幼苗(P DNA)或从中部收集的种子获得的幼苗(M DNA)中提取 DNA。从基因组 DNA 中分离出三种重复序列的片段:高度重复序列(HR),其在大约 2×10(-1)的等效 Cot 内重新关联,以及两个中重复序列(MR1 和 MR2),其 Cot 范围分别约为 2×10(-1)-2 和 2-10(2)。变性动力学允许在每个重复 DNA 片段内识别不同的序列家族,并显示 P 和 M DNA 之间序列重复出现显著差异,特别是对于 MR2 片段而言。大多数 DNA 序列家族在 P DNA 中的表达比在 M DNA 中更丰富。然而,某些序列的冗余性在后者中比在前者中更大。每个重复 DNA 片段与基因组 P 或 M DNA 的 Southern 印迹杂交,这些 DNA 用三对异源同尾限制性内切酶完全消化,这些内切酶对识别位点中胞嘧啶的甲基化不敏感或敏感。结果表明,H. annuus 的重复 DNA 高度甲基化。发现 P 和 M DNA 的甲基化程度存在明显差异,这些差异在 MR2 片段中尤为明显。建议改变特定 DNA 序列的冗余性并改变其甲基化模式是在物种内产生连续遗传变异性的互补方式,可以在环境适应中加以利用。