Bird A P, Taggart M H, Smith B A
Cell. 1979 Aug;17(4):889-901. doi: 10.1016/0092-8674(79)90329-5.
Sea urchin (Echinus esculentus) DNA has been separated into high and low molecular weight fractions by digestion with the mCpG-sensitive restriction endonucleases Hpa II, Hha I and Ava I. The separation was due to differences in methylation at the recognition sequences for these enzymes because an mCpG-insensitive isoschizomer of Hpa II (Msp I) digested Hpa II-resistant DNA to low molecular weight, showing that many Hpa II sites were in fact present in this fraction; and because 3H-methyl methionine administered to embryos was incorporated into the high molecular weight Hpa II-, Hha I- and Ava I-resistant fraction, but not significantly into the low molecular weight fraction. The fraction resistant to Hpa II, Hha I and Ava I amounted to about 40% of the total DNA. It consisted of long sequence tracts between 15 and well over 50 kg in length, in which many sites for each of these enzymes were methylated consecutively. The remaining 60% of the genome, (m-), was not significantly methylated. Methylated and unmethylated fractions were considered to be subfractions of the genome because enriched unique sequences from one fraction cross-reassociated poorly with the other fraction and specific sequences were found in either (m+) or (m-) but not in both (see below). Similar (m+) and (m-) compartments were found in embryos, germ cells and adult somatic tissues. Furthermor, we found no evidence for changes in the sequence composition of (m+) or (m-) between sperm, embryo or intestine DNAs, although low levels of exchange would not have been detected. Using cloned Echinus histone DNA, heterologous 5S DNA and ribosomal DNA probes, we have found that each of these gene families belongs to the unmethylated DNA compartment in all the tissues examined. In particular, there was no detectable methylation of histone DNA either in early embryos, which are thought to be actively transcribing the bulk of histone genes, or in sperm and gastrulae, in which most histone genes are not being transcribed. In contrast to these gene families, sequences complementary to an internally repetitious Echinus DNA clone were found primarily in the methylated DNA compartment.
用对甲基化胞嘧啶-鸟嘌呤敏感的限制性内切酶Hpa II、Hha I和Ava I消化海胆(Echinus esculentus)DNA,可将其分离为高分子量和低分子量部分。这种分离是由于这些酶识别序列处甲基化程度不同所致,因为Hpa II的一种对甲基化胞嘧啶-鸟嘌呤不敏感的同裂酶(Msp I)能将对Hpa II有抗性的DNA消化成低分子量片段,这表明该部分实际上存在许多Hpa II位点;而且因为给胚胎注射的3H-甲基甲硫氨酸被整合到高分子量的对Hpa II、Hha I和Ava I有抗性的部分,而低分子量部分则没有明显整合。对Hpa II、Hha I和Ava I有抗性的部分约占总DNA的40%。它由长度在15到超过50千碱基之间的长序列片段组成,其中这些酶的许多位点是连续甲基化的。基因组的其余60%(未甲基化部分)没有明显甲基化。甲基化和未甲基化部分被认为是基因组的亚部分,因为来自一个部分的富集独特序列与另一个部分的交叉重结合很差,并且特定序列在甲基化部分(m+)或未甲基化部分(m-)中发现,而不是在两者中都发现(见下文)。在胚胎、生殖细胞和成年体细胞组织中都发现了类似的(m+)和(m-)区室。此外,我们没有发现精子、胚胎或肠DNA的(m+)或(m-)序列组成发生变化的证据,尽管低水平的交换可能未被检测到。使用克隆的海胆组蛋白DNA、异源5S DNA和核糖体DNA探针,我们发现在所有检测的组织中,这些基因家族中的每一个都属于未甲基化的DNA区室。特别是,在早期胚胎(被认为在大量转录组蛋白基因)、精子和原肠胚中,组蛋白DNA均未检测到甲基化,而在这些细胞中大多数组蛋白基因不进行转录。与这些基因家族相反,与一个内部重复的海胆DNA克隆互补的序列主要存在于甲基化的DNA区室中。