Carroll D, Brown D D
Cell. 1976 Apr;7(4):467-75. doi: 10.1016/0092-8674(76)90198-7.
The restriction enzymes Hind III and Hae III cleave Xenopus laevis 5S DNA at one and three sites, respectively, in each repeating unit of approximately 700 base pairs. The cleavage sites for both enzymes have been located within the repeating unit by denaturation mapping of the restriction fragments. The Hind III products and one of the Hae III fragments are variable in length, indicating heterogeneity in the length of the repeating unit in 5S DNA. This length heterogeneity is confined to the major A + T-rich spacer region. Repeating units differ from each other by discrete quanta of approximately 15 base pairs. The A + T-rich spacer has been shown to consist largely of tandem subrepeats of just this size (Brownlee, Cartwright, and Brown, 1974). We suggest that the repeat-length heterogeneity is due to variable numbers of these subrepeats in the spacer regions of the major repeating units.
限制性内切酶Hind III和Hae III分别在非洲爪蟾5S DNA每个约700个碱基对的重复单元中的一个位点和三个位点进行切割。通过对限制性片段的变性图谱分析,已确定这两种酶的切割位点均位于重复单元内。Hind III产物和其中一个Hae III片段的长度是可变的,这表明5S DNA重复单元的长度存在异质性。这种长度异质性仅限于富含A+T的主要间隔区。重复单元彼此之间相差约15个碱基对的离散量。富含A+T的间隔区已被证明主要由这种大小的串联亚重复序列组成(Brownlee、Cartwright和Brown,1974年)。我们认为,重复长度的异质性是由于主要重复单元间隔区中这些亚重复序列的数量不同所致。