Royer H D, Sager R
Sidney Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115.
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5794-8. doi: 10.1073/pnas.76.11.5794.
Methylation patterns of Chlamydomonas chloroplast DNAs (chlDNAs) were examined in the vegetative, gametic, and zygotic stages of the life cycle. Restriction endo-nuclease fragment patterns produced by EcoRI, BamHI, Hpa II, and Msp I were compared; the last two cleave DNA at the sequence C-C-G-G, but Hpa II is blocked by prior methylation of the internal cytidine whereas Msp I is not. chlDNAs from vegetative cells of both mating types showed no evidence of methylation at C-C-G-G. Gametic mt+ chlDNA was heavily methylated at C-C-G-G, whereas the homologous chlDNA from mt- gametes showed very slight methylation at C-C-G-G. Methylation of additional sites in chlDNA from mt+ gametes but not from mt- gametes was shown by blockage of some EcoRI and BamHI sites that were cleaved in the chlDNA from vegetative cells. chlDNA from 6-hr zygotes was much more methylated than gametic mt+ DNA, as shown by its almost total resistance to cleavage by all four restriction enzymes. These findings support and extend previous evidence that chlDNA of mt+ cells is methylated during gametogenesis and that further methylation occurs after gametic fusion in the young zygotes.
在衣藻叶绿体DNA(chlDNA)的生命周期中的营养体、配子体和合子体阶段,对其甲基化模式进行了研究。比较了由EcoRI、BamHI、Hpa II和Msp I产生的限制性内切酶片段模式;后两种酶在序列C-C-G-G处切割DNA,但Hpa II会被内部胞嘧啶的预先甲基化所阻断,而Msp I则不会。来自两种交配型营养细胞的chlDNA在C-C-G-G处没有甲基化的迹象。配子体mt+ chlDNA在C-C-G-G处高度甲基化,而来自mt-配子的同源chlDNA在C-C-G-G处显示出非常轻微的甲基化。通过一些在营养细胞的chlDNA中被切割的EcoRI和BamHI位点的阻断,表明mt+配子的chlDNA中存在其他位点的甲基化,而mt-配子的chlDNA中则没有。6小时合子的chlDNA比配子体mt+ DNA甲基化程度高得多,这通过其对所有四种限制性酶的切割几乎完全抗性得以体现。这些发现支持并扩展了先前的证据,即mt+细胞的chlDNA在配子发生过程中被甲基化,并且在年轻合子的配子融合后会发生进一步的甲基化。