Lindberg Hanna K, Falck Ghita C-M, Järventaus Hilkka, Norppa Hannu
New Technologies and Risks, Work Environment Development, Finnish Institute of Occupational Health, Topeliuksenkatu 41aA, FI-00250 Helsinki, Finland.
Mutagenesis. 2008 Sep;23(5):371-6. doi: 10.1093/mutage/gen027. Epub 2008 May 22.
Micronuclei (MN), used as a biomarker of effect in exposure to genotoxic carcinogens, derive from chromosomes and chromosomal fragments lagging behind in anaphase. The two types of MN are usually distinguished from each other by centromeric fluorescence in situ hybridization (FISH), centromere-positive (C(+)) MN representing entire chromosomes and centromere-negative (C(-)) MN chromosomal fragments. The incorporation of various types of chromosomal fragments and chromosomes and chromatids to MN is still poorly understood. We used directly labelled pancentromeric and pantelomeric DNA probes to examine the contents of MN in cultured binucleate lymphocytes of four unexposed, healthy subjects (two men and two women) 35-56 years of age. The presence and number of telomeric and centromeric signals was evaluated in 200 MN (50 MN per subject). These data were used to estimate the proportion of MN harbouring terminal/interstitial fragments, acentric/centric fragments, chromatid-type/chromosome-type fragments and entire chromatids/chromosomes. The majority of the C(+) MN (96% in men and 86% in women) found contained telomeric (T(+)) sequences. Most of the C(+) T(+) MN had one centromere and two or one telomere signals, suggesting that single chromatids were more frequently involved in MN than both sister chromatids. Among the C(-) MN, telomere signals were found in 91% (men) and 79% (women), showing that fragments in MN were mostly terminal. Most C(-) T(+) MN had one telomere signal, indicating higher prevalence for chromatid-type than chromosome-type terminal fragments. Combined centromeric and telomeric FISH is expected to increase the sensitivity of detecting exposure-related effects, when the exposure induces specific types of MN and its effect is low. This approach could particularly have use in discriminating between MN harbouring chromatid- and chromosome-type fragments in studies of human exposure to chemical clastogens and ionizing radiation.
微核(MN)作为暴露于遗传毒性致癌物时效应的生物标志物,源自染色体和在后期滞后的染色体片段。通常通过着丝粒荧光原位杂交(FISH)将两种类型的微核彼此区分开来,着丝粒阳性(C(+))微核代表整条染色体,着丝粒阴性(C(-))微核代表染色体片段。各种类型的染色体片段、染色体和染色单体并入微核的情况仍知之甚少。我们使用直接标记的全着丝粒和全端粒DNA探针,来检测4名35 - 56岁未暴露的健康受试者(2名男性和2名女性)培养的双核淋巴细胞中微核的内容物。在200个微核(每位受试者50个微核)中评估端粒和着丝粒信号的存在和数量。这些数据用于估计含有末端/间质片段、无着丝粒/有着丝粒片段、染色单体型/染色体型片段以及整条染色单体/染色体的微核比例。所发现的大多数C(+)微核(男性中为96%,女性中为86%)含有端粒(T(+))序列。大多数C(+) T(+)微核有一个着丝粒和两个或一个端粒信号,这表明与两条姐妹染色单体相比,单条染色单体更频繁地参与微核形成。在C(-)微核中,91%(男性)和79%(女性)发现有端粒信号,表明微核中的片段大多是末端片段。大多数C(-) T(+)微核有一个端粒信号,表明染色单体型末端片段比染色体型末端片段更普遍。当暴露诱导特定类型的微核且其效应较小时,联合着丝粒和端粒FISH有望提高检测暴露相关效应的灵敏度。这种方法在人类接触化学断裂剂和电离辐射的研究中,对于区分含有染色单体型和染色体型片段的微核可能特别有用。