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p53基因缺陷小鼠中的自发及电离辐射诱导的染色体异常

Spontaneous and ionizing radiation-induced chromosomal abnormalities in p53-deficient mice.

作者信息

Bouffler S D, Kemp C J, Balmain A, Cox R

机构信息

Biomedical Effects Department, National Radiological Protection Board, Didcot, Oxon, United Kingdom.

出版信息

Cancer Res. 1995 Sep 1;55(17):3883-9.

PMID:7641208
Abstract

Chromosomal abnormalities have been assessed in p53-deficient mice. The in vivo frequency of spontaneous stable aberrations in bone marrow cells was elevated by approximately 20-fold in p53 nulls and 13-fold in p53 heterozygotes compared to wild-type. No excessive induction of stable aberrations by gamma-irradiation was observed, but p53 deficiency resulted in excess radiation-induced hyperploidy (> 10-fold wild-type frequency). No influence of p53 genotype on sister chromatid exchange or G2 chromatid damage was observed in mitogen-stimulated spleen cell cultures; however, a p53 effect on postirradiation mitotic entry was seen. Abnormalities in chromosome segregation and mitotic delay following irradiation in p53-deficient mice suggest a G2-M checkpoint role for p53 and are broadly consistent with data on tumorigenesis in these animals.

摘要

已经对p53基因缺陷型小鼠的染色体异常情况进行了评估。与野生型相比,p53基因敲除小鼠骨髓细胞中自发稳定畸变的体内频率升高了约20倍,p53杂合子小鼠则升高了13倍。未观察到γ射线照射对稳定畸变有过度诱导作用,但p53基因缺陷导致辐射诱导的超倍体过多(>野生型频率的10倍)。在有丝分裂原刺激的脾细胞培养物中,未观察到p53基因型对姐妹染色单体交换或G2期染色单体损伤有影响;然而,观察到了p53对辐射后有丝分裂进入的影响。p53基因缺陷型小鼠在辐射后出现染色体分离异常和有丝分裂延迟,这表明p53在G2-M期检查点发挥作用,并且与这些动物的肿瘤发生数据大致相符。

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