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与细胞动力学相关的诱导性和自发性染色体畸变的频率及类型

Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics.

作者信息

Mutchinick O, Ruz L, Gonsebatt M E, Mauleón P, Lisker R, García G

出版信息

Hum Genet. 1981;59(2):137-40. doi: 10.1007/BF00293063.

DOI:10.1007/BF00293063
PMID:7327573
Abstract

Induced and spontaneous structural chromosome aberrations (SCA) were studied in a child accidentally radiated with a high dose of 192Ir, and in three sibs with Fanconi's anemia, analyzing by separate first division metaphases (FDM) and second division metaphases (SDM). The results showed that the number of SCA, number of cells with aberrations, and SCA per cell were markedly higher in FDM in all patients. Furthermore, for some type of structural changes like dicentric chromosomes and chromatid interchanges, the differences were particularly striking. The importance of ascertaining FDM identified with proper techniques, for the study of the clastogenic effect of environmental agents and some aspects related to the differences in cytogenetic features found in diverse tissues in Fanconi's anemia are discussed.

摘要

对一名意外受到高剂量¹⁹²铱辐射的儿童以及三名患有范可尼贫血的同胞进行了诱导性和自发性染色体结构畸变(SCA)研究,通过单独的第一次分裂中期(FDM)和第二次分裂中期(SDM)进行分析。结果显示,所有患者的FDM中SCA数量、有畸变的细胞数量以及每个细胞的SCA数量均显著更高。此外,对于某些类型的结构变化,如双着丝粒染色体和染色单体互换,差异尤为显著。本文讨论了采用适当技术确定FDM对于研究环境因素的致断裂效应以及范可尼贫血不同组织中细胞遗传学特征差异相关某些方面的重要性。

相似文献

1
Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics.与细胞动力学相关的诱导性和自发性染色体畸变的频率及类型
Hum Genet. 1981;59(2):137-40. doi: 10.1007/BF00293063.
2
[Relationship of spontaneous chromosome instability and sister chromatid exchanges in Fanconi's anemia].[范可尼贫血中自发染色体不稳定性与姐妹染色单体交换的关系]
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The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts.在范科尼贫血中,姐妹染色单体交换率与自发染色体断裂平行,在人类淋巴细胞和成纤维细胞中与三胺硫磷诱导的畸变平行。
Humangenetik. 1975 Sep 23;29(3):201-6. doi: 10.1007/BF00297624.
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Effects of alkylating agents on lymphocytes from controls and from patients with Fanconi's anemia. Studies of sister chromatid exchanges, chromosome aberrations, and kinetics of cell division.烷化剂对对照组及范科尼贫血患者淋巴细胞的影响。姐妹染色单体交换、染色体畸变及细胞分裂动力学研究。
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Position of chromosomes in the human interphase nucleus. An analysis of nonhomologous chromatid translocations in lymphocyte cultures after Trenimon treatment and from patients with Fanconi's anemia and Bloom's syndrome.人类间期细胞核中染色体的位置。对经三胺硫磷处理后的淋巴细胞培养物以及范科尼贫血和布卢姆综合征患者的非同源染色单体易位的分析。
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Hum Genet. 1979;52(3):309-21. doi: 10.1007/BF00278680.

引用本文的文献

1
The cell cycle of lymphocytes in Fanconi anemia.范可尼贫血中淋巴细胞的细胞周期
Hum Genet. 1982;62(4):327-32. doi: 10.1007/BF00304549.
2
Cytogenetic analyses utilizing various clastogens in two sibs with Fanconi anemia, their relatives, and control individuals.利用各种致断裂剂对两名范可尼贫血患者及其亲属和对照个体进行细胞遗传学分析。
Hum Genet. 1985;69(4):309-15. doi: 10.1007/BF00291647.

本文引用的文献

1
CHROMOSOME INVESTIGATIONS ON LYMPHOCYTES FROM IRRADIATED PATIENTS: EFFECT OF TIME IN CULTURE.对受辐照患者淋巴细胞的染色体研究:培养时间的影响。
Nature. 1964 May 16;202:714-5. doi: 10.1038/202714a0.
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Time of first-generation metaphases. I. The effect of various culture media and of fetal calf serum in human lymphocyte cultures.
Mutat Res. 1980 Aug;72(1):127-34. doi: 10.1016/0027-5107(80)90228-6.
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Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method.通过细胞遗传学方法对范可尼贫血进行产前和产后诊断及携带者检测。
Pediatrics. 1981 Jan;67(1):128-35.
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Chromosome abnormalities in constitutional aplastic anemia.先天性再生障碍性贫血中的染色体异常
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Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease.遗传性疾病中的自发染色体断裂和白血病高发病率。
Blood. 1971 Jan;37(1):96-112.
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Defective DNA repair in Fanconi's anaemia.范科尼贫血中的DNA修复缺陷。
Nature. 1974 Jul 19;250(463):223-5. doi: 10.1038/250223a0.
8
The human leukocyte test system. I. DNA synthesis and mitoses in PHA-stimulated 2-day cultures.人类白细胞检测系统。I. 植物血凝素刺激的2日龄培养物中的DNA合成与有丝分裂。
Mutat Res. 1974 May;23(2):279-81.
9
Ataxia-telangiectasia--clonal growth of translocation lymphocytes.共济失调毛细血管扩张症——易位淋巴细胞的克隆性生长。
N Engl J Med. 1973 Aug 9;289(6):286-91. doi: 10.1056/NEJM197308092890603.
10
Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement.布卢姆综合征和范科尼贫血:两种独特的染色体断裂和重排模式的证明。
Humangenetik. 1974;25(4):299-306. doi: 10.1007/BF00336905.