Callan H G, Gall J G, Berg C A
Chromosoma. 1987;95(4):236-50. doi: 10.1007/BF00294780.
Details are given of a technique for making permanent preparations of the lampbrush chromosomes of Xenopus laevis. Stained preparations allow all 18 bivalent chromosomes to be identified, and a working map showing the major features has been constructed. Fifteen of the Xenopus chromosomes have one telomere conspicuously larger than the other; the two smallest chromosomes, and one other, lack large telomeres. Similar preparations, extracted with RNase and denatured, have been hybridized in situ with a 3H-labelled 5S cRNA probe. Chromosomes can be identified in the resulting autoradiographs. 5S DNA sequences are present at all the larger telomeres and at three of the smaller ones, but are absent from the telomeres at both ends of the two smallest chromosomes. There are also five interstitial sites of hybridization. At one of these, label is on the chromosome axis; at the other four, label extends well away from the axis.
本文详细介绍了一种制备非洲爪蟾灯刷染色体永久标本的技术。经染色的标本能够识别出所有18条二价染色体,并构建了显示其主要特征的工作图谱。非洲爪蟾的15条染色体中,有一条端粒明显大于另一条;两条最小的染色体以及另外一条染色体缺乏大的端粒。用核糖核酸酶提取并变性后的类似标本,已与3H标记的5S cRNA探针进行原位杂交。在所得的放射自显影片中可以识别出染色体。5S DNA序列存在于所有较大的端粒以及三个较小的端粒中,但在两条最小染色体两端的端粒中不存在。此外还有五个杂交的间质位点。其中一个位点的标记位于染色体轴上;在另外四个位点,标记远离染色体轴延伸。