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减数分裂前事件与减数分裂染色体配对

Premeiotic events and meiotic chromosome pairing.

作者信息

Bennett M D

出版信息

Symp Soc Exp Biol. 1984;38:87-121.

PMID:6400221
Abstract

There is practical difficulty in identifying when meiosis begins. Moreover, because of contradictory definitions there is ambiguity and some confusion as to when, in terms of the cell cycle, premeiosis ends and meiosis begins. Nevertheless, results for several organisms show clearly that meiotic chromosome behaviour is affected by premeiotic events and especially by events during the final premeiotic mitosis and/or premeiotic interphase. This review considers only premeiotic events which do (or might) affect meiotic chromosome pairing by their effect on genomic characters, such as: chromosome number, homology, condition and position, with particular emphasis on the last. Interpreted in its widest sense 'premeiotic events affecting meiotic chromosome pairing' must include karyogamy. Moreover, while karyogamy is the normal means of achieving the diploid chromosome number and pairs of homologues essential for normal chromosome pairing, it is not the only way, as illustrated by the remarkable premeiotic adaptations seen in the apogamous ferns and the frog Rana esculenta. Little is known about the condition (including the molecular organization) of chromosomes during their approach and switch to meiosis. However, completion during premeiosis of some DNA synthesis may be essential for normal meiotic chromosome pairing. Various results (including different effects of colchicine given first at different premeiotic stages) have been claimed as evidence of one or other type of premeiotic spatial ordering of chromosomes which might favour, or be essential for, meiotic chromosome pairing. Chromosome placement has been studied recently using the electron microscope, serial thin-section, reconstruction technique. This has revealed clear evidence of non-random spatial placement of chromosomes in non-meiotic and premeiotic cells. For example, in root-tip cells of barley, Hordeum vulgare L. cv. Tuleen 346 (2n = 2x = 14), it showed: a significant spatial separation of two haploid chromosome sets; no somatic association of homologues; but a significant expression of a predicted mean order of heterologues (namely, linkage groups -4-1-2-3-5-6-7-) within haploid sets. This spatial arrangement of chromosomes might have important implications for the switch from premeiotic to meiotic development, if it occurred in germ line cells. Consequently, metaphase cells of Tuleen 346 at the final premeiotic mitosis were reconstructed next. Analysis of centromere positions showed a significantly ordered arrangement of haploid sets, and of heterologues within haploid sets, essentially the same as that previously noted for root-tip cells.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

确定减数分裂何时开始存在实际困难。此外,由于定义相互矛盾,关于在细胞周期中减数分裂前阶段何时结束以及减数分裂何时开始存在模糊性和一些混淆。然而,几种生物体的研究结果清楚地表明,减数分裂染色体行为受减数分裂前事件的影响,特别是受最后一次减数分裂前有丝分裂和/或减数分裂前间期事件的影响。本综述仅考虑那些确实(或可能)通过影响基因组特征来影响减数分裂染色体配对的减数分裂前事件,例如:染色体数目、同源性、状态和位置,特别强调最后一点。从最广泛的意义上讲,“影响减数分裂染色体配对的减数分裂前事件”必须包括核配。此外,虽然核配是实现正常染色体配对所必需的二倍体染色体数目和同源染色体对的正常方式,但它不是唯一的方式,无融合生殖蕨类植物和食用蛙(Rana esculenta)中显著的减数分裂前适应现象就说明了这一点。关于染色体在接近和转向减数分裂过程中的状态(包括分子组织)知之甚少。然而,减数分裂前完成一些DNA合成可能对正常的减数分裂染色体配对至关重要。各种结果(包括在不同减数分裂前阶段首次给予秋水仙素的不同影响)被认为是一种或另一种减数分裂前染色体空间排列类型的证据,这种排列可能有利于或对减数分裂染色体配对至关重要。最近使用电子显微镜、连续薄切片重建技术对染色体定位进行了研究。这揭示了非减数分裂和减数分裂前细胞中染色体非随机空间定位的明确证据。例如,在大麦(Hordeum vulgare L. cv. Tuleen 346,2n = 2x = 14)的根尖细胞中,研究显示:两个单倍体染色体组有明显的空间分离;同源染色体无体细胞关联;但单倍体组内预测的异源染色体平均顺序(即连锁群-4-1-2-3-5-6-7-)有显著表达。如果这种染色体的空间排列发生在生殖细胞中,那么它可能对从减数分裂前发育向减数分裂发育的转变具有重要意义。因此,接下来对图林346(Tuleen 346)减数分裂前最后一次有丝分裂的中期细胞进行了重建。着丝粒位置分析显示单倍体组以及单倍体组内异源染色体有明显的有序排列,基本上与之前在根尖细胞中观察到的相同。(摘要截断于400字)

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