Koo Dal-Hoe, Jiang Jiming
Department of Horticulture, University of Wisconsin-Madison, Madison, WI 53706, USA.
Plant J. 2009 Aug;59(3):509-16. doi: 10.1111/j.1365-313X.2009.03881.x. Epub 2009 Mar 30.
Meiotic pachytene chromosome-based fluorescence in situ hybridization (FISH) mapping is one of the most important tools in plant molecular cytogenetic research. Here we report a simple technique that allows stretching of pachytene chromosomes of maize to up to at least 20 times their original size. A modified Carnoy's II fixative (6:1:3 ethanol:chloroform:acetic acid) was used in the procedure, and proved to be key for super-stretching of pachytene chromosomes. We demonstrate that super-stretched pachytene chromosomes provide unprecedented resolution for chromosome-based FISH mapping. DNA probes separated by as little as 50 kb can be resolved on super-stretched chromosomes. A combination of FISH with immunofluorescent detection of 5-methyl cytosine on super-stretched pachytene chromosomes provides a powerful tool to reveal DNA methylation of specific chromosomal domains, especially those associated with highly repetitive DNA sequences.
基于减数分裂粗线期染色体的荧光原位杂交(FISH)图谱绘制是植物分子细胞遗传学研究中最重要的工具之一。在此,我们报道了一种简单的技术,该技术可将玉米粗线期染色体拉伸至其原始大小的至少20倍。在该过程中使用了改良的卡诺氏II固定液(乙醇∶氯仿∶乙酸为体积比6∶1∶3),事实证明这是粗线期染色体超拉伸的关键。我们证明,超拉伸的粗线期染色体为基于染色体的FISH图谱绘制提供了前所未有的分辨率。在超拉伸染色体上可以分辨出间隔仅50 kb的DNA探针。将FISH与超拉伸粗线期染色体上5-甲基胞嘧啶的免疫荧光检测相结合,提供了一个强大的工具来揭示特定染色体区域的DNA甲基化,尤其是那些与高度重复DNA序列相关的区域。