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在含有热不稳定DNA聚合酶α的小鼠温度敏感突变体tsFT20品系中,对在限制温度下孵育诱导的染色体畸变进行表征。

Characterization of chromosome aberrations induced by incubation at a restrictive temperature in the mouse temperature-sensitive mutant tsFT20 strain containing heat-labile DNA polymerase alpha.

作者信息

Eki T, Enomoto T, Murakami Y, Hanaoka F, Yamada M

出版信息

Cancer Res. 1987 Oct 1;47(19):5162-70.

PMID:3621201
Abstract

tsFT20 cells derived from a mouse mammary carcinoma cell line, FM3A, which has temperature-sensitive DNA polymerase alpha activity (Y. Murakami, H. Yasuda, H. Miyazawa, F. Hanaoka, and M. Yamada, Proc. Natl. Acad. Sci. USA, 82:1761-1765, 1985) were rapidly committed to death after temperature upshift to 39 degrees C. tsFT20 cells synchronized in S phase were more sensitive to the restrictive temperature than exponentially growing cells. In order to gain insight into the processes from the interruption of DNA synthesis to cell death, we analyzed chromosome aberrations induced in tsFT20 cells which had been incubated for 2 or 4 h at the restrictive temperature and then cultured at the permissive temperature. The majority of metaphase cells showed extensive chromosome aberrations such as chromatid gaps, breaks, and exchanges; chromosome pulverizations; their mixed types; and ring chromosomes. Analyses with the use of cell synchronization and autoradiography revealed that chromosome aberrations were induced only in the cells which synthesized DNA during incubation at 39 degrees C. We classified the chromosome aberrations into five types: gap or break type; exchange type; pulverization type; complex type; and ring type. The temporal order of the appearance of these types of chromosome aberrations was found to be the above described order. It was further found that cycloheximide dramatically repressed the induction of chromosome aberrations, and metaphases with many chromosome aberrations exhibited a large number of sister chromatid exchanges. These results indicate that abnormal cessation of DNA replication in tsFT20 cells at the restrictive temperature due to the inactivation of DNA polymerase alpha results in cell death via induction of double-strand breaks which lead to chromosome aberrations as well as sister chromatid exchanges.

摘要

tsFT20细胞源自小鼠乳腺癌细胞系FM3A,该细胞系具有温度敏感的DNA聚合酶α活性(Y. 村上、H. 安田、H. 宫泽、F. 花冈和M. 山田,《美国国家科学院院刊》,82:1761 - 1765,1985),在温度升至39℃后迅速走向死亡。处于S期同步化的tsFT20细胞比指数生长的细胞对限制温度更敏感。为了深入了解从DNA合成中断到细胞死亡的过程,我们分析了在限制温度下培养2或4小时然后在允许温度下培养的tsFT20细胞中诱导产生的染色体畸变。大多数中期细胞显示出广泛的染色体畸变,如染色单体间隙、断裂和交换;染色体粉碎;它们的混合类型;以及环状染色体。使用细胞同步化和放射自显影分析表明,染色体畸变仅在39℃培养期间合成DNA的细胞中诱导产生。我们将染色体畸变分为五种类型:间隙或断裂型;交换型;粉碎型;复合型;和环状型。发现这些类型的染色体畸变出现的时间顺序是上述顺序。还发现环己酰亚胺显著抑制染色体畸变的诱导,并且具有许多染色体畸变的中期细胞表现出大量的姐妹染色单体交换。这些结果表明,在限制温度下,由于DNA聚合酶α失活,tsFT20细胞中DNA复制异常停止,通过诱导双链断裂导致细胞死亡,并进而导致染色体畸变以及姐妹染色单体交换。

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