Department of Plant Biology, Carnegie Institution of Washington, 290 Panama Street, 94305, Stanford, CA, U.S.A..
Plant Mol Biol. 1987 Jan;8(1):3-12. doi: 10.1007/BF00016429.
A complete ribosomal DNA (rDNA) repeat unit has been cloned from the genome of Pisum sativum (garden pea) and used to construct a map containing a total of 58 cleavage sites for 23 different restriction enzymes. Regions encoding 18s and 25s ribosomal RNA (rRNA) were identified by R-loop analysis. A 180 bp sequence element is repeated eight times in the intergenic 'nontranscribed spacer' (NTS) region, as defined by eight evenly spaced RsaI cleavage sites. Sequence heterogeneity among these elements (subrepeats) is indicated by the presence of an NcoI site within the five RsaI subrepeats distal to the 25s rRNA gene but not in the three subrepeats proximal to this gene, and also by the presence of an additional RsaI cleavage site in one subrepeat.The approximately 4000 copies of the rDNA repeat in the pea nuclear genome show considerable heterogeneity with respect to the length of the NTS region, and differences are also frequently observed between different genotypes. In both cases the length variation appears to be due primarily to differences in the number of subrepeat elements.Comparison of rDNA restriction maps for two pea genotypes separated for hundreds or perhaps thousands of generations reveals that they contain many rDNA identical repeat units. This data is consistent with the view that new rDNA variants are fixed only infrequently in the evolution of a species.Differences also exist between the rDNA repeats of a single genotype with respect to the degree of base modification at certain restriction sites. A large number of sites known to exist in the pea rDNA clone are not cleaved at all in genomic rDNA, or are cleaved in only some copies of the rDNA repeat. We believe these examples of incomplete cleavage results mostly from methylation, although it is difficult to rule out the possibility of sequence variation in all cases. Most putative modifications are best interpreted in terms of cytosine methylation in CG and CXG sequences, but at least one example is more consistent with adenine methylation.We also have constructed a more detailed restriction map of the wheat rDNA clone pTA71 and present a comparison of this map to our map of pea, pumpkin, and wheat in order to assess the amount of useful evolutionary information that can be obtained by comparison of such maps.
从豌豆基因组中克隆出一个完整的核糖体 DNA(rDNA)重复单元,并用于构建一个包含 23 种不同限制酶的总共 58 个切割位点的图谱。通过 R 环分析鉴定编码 18s 和 25s 核糖体 RNA(rRNA)的区域。在基因间“非转录间隔区”(NTS)区域中,一个 180bp 的序列元件重复 8 次,由 8 个均匀间隔的 RsaI 切割位点定义。这些元件(亚重复)之间的序列异质性由 NcoI 位点表示,该位点存在于靠近 25s rRNA 基因的 5 个 RsaI 亚重复中,但不存在于靠近该基因的 3 个亚重复中,并且在一个亚重复中还存在另外一个 RsaI 切割位点。豌豆核基因组中的 rDNA 重复约有 4000 个拷贝,在 NTS 区域的长度上具有很大的异质性,并且在不同基因型之间也经常观察到差异。在这两种情况下,长度变化似乎主要是由于亚重复元件数量的差异。比较两个豌豆基因型的 rDNA 限制图谱,它们已经分离了数百代甚至数千代,结果表明它们包含许多相同的 rDNA 重复单元。这一数据与物种进化过程中 rDNA 新变体很少固定的观点一致。在单个基因型的 rDNA 重复之间,某些限制位点的碱基修饰程度也存在差异。大量已知存在于豌豆 rDNA 克隆中的位点在基因组 rDNA 中根本不被切割,或者仅在 rDNA 重复的某些拷贝中被切割。我们认为这些不完全切割的例子主要是由于甲基化所致,尽管在所有情况下都很难排除序列变异的可能性。大多数假定的修饰最好用 CG 和 CXG 序列中的胞嘧啶甲基化来解释,但至少有一个例子更符合腺嘌呤甲基化。我们还构建了小麦 rDNA 克隆 pTA71 的更详细限制图谱,并将该图谱与我们的豌豆、南瓜和小麦图谱进行了比较,以评估通过比较此类图谱可以获得多少有用的进化信息。