Allis C D, Colavito-Shepanski M, Gorovsky M A
Verna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030.
Dev Biol. 1987 Dec;124(2):469-80. doi: 10.1016/0012-1606(87)90500-8.
Autoradiography has been used to confirm and to extend previous microspectrophotometric studies (Doerder and DeBault, 1975) on the timing of DNA synthesis during conjugation in Tetrahymena thermophila. The majority of DNA synthesis occurs at the expected periods preceding gamete formation and the two postzygotic divisions and during macronuclear development. DNA in new macronuclei is endoreplicated in an extremely discontinuous fashion. Under starvation conditions, the first endoreplication (2C to 4C) occurs immediately after the second postzygotic division when both new macronuclei and new micronuclei replicate. The second endoreplication (4C to 8C) does not occur until after separation of conjugants. If mating cells are kept under prolonged starvation conditions (20-24 hr), refeeding induces a partially synchronous division, after which an unexpectedly high percentage of cells incorporate tritiated thymidine into both macro- and micronuclei. Two previously undescribed periods of DNA synthesis were observed in the micronuclei of conjugating Tetrahymena. The first occurs during the early stages of meiotic prophase, before full crescent elongation. The second takes place in an extended period corresponding to macronuclear anlagen development, before conjugants have separated. CsCl gradient analyses indicate that, in micronuclear fractions, only main band DNA is being synthesized in both of these periods. However, in macronuclear fractions from both stages, a significant fraction (approximately 20%) of the DNA being synthesized has the buoyant density of ribosomal DNA. The finding that macro- and micronuclear DNA can be synthesized simultaneously in a single cell, both during conjugation and after refeeding starved exconjugants, raises interesting questions of how macro- or micronuclear-specific histones are targeted to the appropriate nuclei.
放射自显影已被用于证实并拓展先前关于嗜热四膜虫接合过程中DNA合成时间的显微分光光度研究(Doerder和DeBault,1975年)。大多数DNA合成发生在配子形成之前、合子后两次分裂之前以及大核发育期间的预期阶段。新大核中的DNA以极其不连续的方式进行核内复制。在饥饿条件下,第一次核内复制(从2C到4C)在合子后第二次分裂后立即发生,此时新的大核和新的小核都进行复制。第二次核内复制(从4C到8C)直到接合体分离后才发生。如果交配细胞长时间处于饥饿条件下(20 - 24小时),重新喂食会诱导部分同步分裂,之后有意外高比例的细胞将氚标记的胸腺嘧啶核苷掺入大核和小核中。在接合的嗜热四膜虫的小核中观察到两个先前未描述的DNA合成时期。第一个时期发生在减数分裂前期的早期阶段,在新月体完全伸长之前。第二个时期发生在与大核原基发育相对应的延长阶段,在接合体分离之前。氯化铯梯度分析表明,在小核部分,这两个时期都只有主带DNA在合成。然而,在这两个阶段的大核部分,合成的DNA中有相当一部分(约20%)具有核糖体DNA的浮力密度。在接合过程中以及给饥饿的接合后细胞重新喂食后,大核和小核DNA能在单个细胞中同时合成,这一发现引发了关于大核或小核特异性组蛋白如何靶向到合适细胞核的有趣问题。