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首页> 外文期刊>Mutagenesis >Spontaneous and spindle poison-induced micronuclei and chromosome non-disjunction in cytokinesis-blocked lymphocytes from two age groups of women.
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Spontaneous and spindle poison-induced micronuclei and chromosome non-disjunction in cytokinesis-blocked lymphocytes from two age groups of women.

机译:自发性和纺锤体中毒诱导的两个年龄段女性的胞质分裂阻滞淋巴细胞中的微核和染色体不分离。

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摘要

Fluorescence in situ hybridization (FISH) was used to evaluate spontaneous and aneuploidogen-induced micronucleus frequencies and non-disjunction of chromosomes X and 8 in cultured binucleated lymphocytes of women of two age groups. Demecolcine and vincristine were used as model aneuploidogens to induce micronuclei and chromosome malsegregation. Four of the women were aged 22-26 (mean 24.3) years and four 47-50 (mean 49.0) years. Pancentromeric FISH was applied to micronuclei to identify chromosomes and double-color centromeric FISH, performed in binucleates of two young and two older women, was used to assess the involvement of chromosomes X and 8 in micronuclei and non-disjunction. It was confirmed that age increases micronucleus frequency. Micronuclei containing whole chromosomes predominated in older females. Age also enhanced micronuclei containing acentric chromosome fragments. The inclusion of chromosomes X and 8 in micronuclei was enhanced by age and chromosome X was generally overrepresented. Non-disjunction of chromosomes X and 8 also increased with age, chromosome X being the more sensitive. Treatment of lymphocytes with vincristine and demecolcine increased micronucleus frequency and malsegregation of chromosomes X and 8 in both age groups. Comparison of the estimated frequencies of micronucleation and non-disjunction for all human chromosomes showed that non-disjunction is the main type of chromosome malsegregation.
机译:荧光原位杂交(FISH)用于评估两个年龄组的女性培养的双核淋巴细胞中自发和非整倍体诱导的微核频率以及X和8号染色体的不分离。地美可辛和长春新碱被用作模型非整倍性原,以诱导微核和染色体错误分离。其中四名妇女的年龄为22-26岁(平均24.3岁),四名妇女为47-50岁(平均49.0岁)。将Pancentromeric FISH应用于微核以鉴定染色体,并在两名年轻和两名老年妇女的双核中进行双色着丝粒FISH,以评估X和8号染色体参与微核和非分离。证实年龄增加了微核频率。包含完整染色体的微核在老年女性中占主导地位。年龄也增强了包含无心染色体片段的微核。随着年龄的增长,X染色体和8染色体中的夹杂物会增加,X染色体通常被过度代表。 X染色体和8染色体的不分离也随着年龄的增长而增加,X染色体更加敏感。在两个年龄组中,用长春新碱和地美可辛治疗淋巴细胞会增加微核频率,并破坏X和8号染色体的分离。比较所有人类染色体的微核化和不分离的频率,发现不分离是染色体错误分离的主要类型。

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