Natarajan A T, Boei J J W A
Department Toxicogenetics, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL Leiden, The Netherlands.
Mutat Res. 2003 Nov;544(2-3):299-304. doi: 10.1016/j.mrrev.2003.09.005.
Most of the mutagenic and carcinogenic agents induce chromosome aberrations in vivo and in vitro. Conventional solid staining (such as Giemsa) has been employed to evaluate the frequencies and types of spontaneous and induced chromosomal aberrations. Recently, molecular cytogenetic techniques such as fluorescence in situ hybridization (FISH) using chromosome specific or chromosome region-specific DNA libraries have become available, which have increased the resolution of the detection of aberrations. This has lead to a better understanding on the mechanisms of formation of chromosome aberrations, especially following treatment with ionizing radiation. The present paper reviews briefly the results obtained using FISH technique both from basic and applied studies.
大多数诱变剂和致癌剂在体内和体外均可诱导染色体畸变。传统的实体染色法(如吉姆萨染色)已被用于评估自发和诱导染色体畸变的频率及类型。近年来,诸如使用染色体特异性或染色体区域特异性DNA文库的荧光原位杂交(FISH)等分子细胞遗传学技术已得以应用,这些技术提高了畸变检测的分辨率。这使得人们对染色体畸变的形成机制有了更好的理解,尤其是在受到电离辐射处理之后。本文简要综述了基础研究和应用研究中使用FISH技术所获得的结果。