Thomson E J, Perry P E
MRC Clinical and Population Cytogenetics Unit, Western General Hospital, Edinburgh, UK.
Mutagenesis. 1988 Sep;3(5):415-8. doi: 10.1093/mutage/3.5.415.
A technique is presented for establishing the presence of kinetochores in micronuclei (mn) using CREST antikinetochore antibodies and immunofluorescence. In cultured lymphocytes blocked in their second cycle by cytochalasin-B 61% baseline mn possess kinetochores, and thus originated from whole chromosomes. Mn-inducing agents with different modes of action were compared to determine the proportion of mn with kinetochores: virtually all X-ray- and mitomycin-C-induced mn were derived from acentric fragments as shown by the absence of kinetochore immunofluorescence, whereas the majority (79%) of colcemid-induced mn were CREST positive, reflecting the formation of mn through failure of attachment of chromosomes to the spindle. The proportion of mn without kinetochore fluorescence in the control (39%) and colcemid-treated (21%) cultures was greater than expected and possible reasons for this are discussed.
本文介绍了一种使用着丝粒特异性自身抗体(CREST)和免疫荧光技术来确定微核(mn)中着丝粒存在情况的方法。在被细胞松弛素B阻滞于第二个细胞周期的培养淋巴细胞中,61%的基线微核含有着丝粒,因此来源于整条染色体。比较了具有不同作用方式的微核诱导剂,以确定含有着丝粒的微核比例:实际上,所有经X射线和丝裂霉素C诱导产生的微核均来自无着丝粒片段,这可通过着丝粒免疫荧光缺失来证明,而秋水仙酰胺诱导产生的微核中大部分(79%)CREST呈阳性,这反映了微核是由于染色体未能附着于纺锤体而形成的。在对照培养物(39%)和秋水仙酰胺处理的培养物(21%)中,无微着丝粒荧光的微核比例高于预期,并讨论了造成这种情况的可能原因。