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核内复制细胞的双染色体:一种突出姐妹染色单体交换机制的新方法。

The diplochromosome of endoreduplicated cells: a new approach to highlight the mechanism of sister chromatid exchange.

作者信息

Meschini R, Bastianelli R, Palitti F

机构信息

Department of Agrobiology and Agrochemistry, University of Tuscia, Via S. Camillo de Lellis, s.n.c., I-01100 Viterbo, Italy.

出版信息

Chromosoma. 1996 Jul;105(1):50-4. doi: 10.1007/BF02510038.

Abstract

Chinese hamster lung embryonic cells (CL1) were treated with colchicine in order to induce endoreduplication and subsequently with mitomycin-C (MMC) to induce exchanges within the diplochromosome. The use of chromosomal differential staining through incorporation of 5-bromodeoxyuridine, resulting in only one stained chromatid, has allowed the analysis of all classes of exchanges among the four chromatids of the diplochromosome. Three classes of exchanges may occur: intradiplochromatid exchanges (ICEs) between the two inner chromatids, cousin chromatid exchanges (CCEs) between one inner and one outer chromatid, and sister chromatid exchanges (SCEs) between the two sister chromatids of the diplochromosome. The results show that MMC treatment, in the last cell cycle of endoreduplication, as expected, significantly increases only the frequency of SCEs, whereas the frequency of ICEs and CCEs remains unchanged. This result supports replication models of formation of SCEs. Furthermore the fact that the number of ICEs does not increase means that the molecular mechanism of somatic crossing over is not related to that of SCE formation, or very rarely. The results also indicate a statistically significant lower induction of SCEs in endoreduplicated metaphases as compared with diploid ones both in control and MMC-treated cells. Such a result may be due to structural restrictions within the diplochromosome.

摘要

用秋水仙碱处理中国仓鼠肺胚胎细胞(CL1)以诱导核内复制,随后用丝裂霉素-C(MMC)诱导双染色体内部发生交换。通过掺入5-溴脱氧尿苷进行染色体差异染色,结果只有一条染色单体被染色,从而能够分析双染色体四条染色单体之间所有类型的交换。可能发生三类交换:两条内部染色单体之间的双染色体内染色单体交换(ICEs)、一条内部染色单体与一条外部染色单体之间的姐妹染色单体交换(CCEs)以及双染色体两条姐妹染色单体之间的姐妹染色单体交换(SCEs)。结果表明,正如预期的那样,在核内复制的最后一个细胞周期中,MMC处理仅显著增加了SCEs的频率,而ICEs和CCEs的频率保持不变。这一结果支持了SCEs形成的复制模型。此外,ICEs数量没有增加这一事实意味着体细胞交换的分子机制与SCEs形成的机制无关,或者关系非常小。结果还表明,在对照细胞和MMC处理的细胞中,与二倍体中期相比,核内复制中期SCEs的诱导在统计学上显著降低。这样的结果可能是由于双染色体内的结构限制。

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