Length and sequence heterogeneity of the histone gene repeat unit of the sea urchin, S. purpuratus
Length and sequence heterogeneity of the histone gene repeat unit of the sea urchin, S. purpuratus
复制标题
海胆组蛋白基因重复单元的长度和序列异质性
DOI:
10.1016/0092-8674(78)90111-3
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发表时间:
1978
期刊:
影响因子:
64.5
通讯作者:
E. Weinberg
中科院分区:
文献类型:
--
作者:
G. Overton;E. Weinberg
Histone gene repeats in S. purpuratus are shown to be of variable length and sequence. Two recombinant plasmids containing the full-length 6.3 kb histone repeat unit are found to differ in length at two sites in the repeating structure and in the occurrence of two restriction enzyme recognition sites. Variation in repeat length is also demonstrated in the unfractionated DNA of five sea urchins and in a sample of DNA enriched for histone gene sequences by density gradient methods. The repeats in each individual are of a very limited number of major classes, which may differ from one another in overall length or in distribution and presence of particular restriction enzyme sites. Variations are found to occur at many regions of the repeat; some have been mapped specifically to spacer regions. Repeats may differ dramatically from individual to individual since there is no one type of repeat class common to all, although the absolute length differences of the repeats that are found are small. introductionThe histone gene cluster (hDNA) is the most extensively characterized example of repeated DNA coding for structural proteins. In the sea urchin, the coding regions for the five major histone classes are contained in a 6-7 kb repeat unit (Birnstiel et al., 1975; Kedes et al., 1975a, 1975b; Weinberg et al., 1975; Cohn, Lowry and Kedes, 1976; Portmann, Schaffner and Birnstiel, 1976; Schaffner et al., 1976; Wu et al., 1976; Holmes et al., 1977) which is tandemly reiterated several hundred fold (Kedes and Birnstiel, 1971;. Weinberg et al., 1972; Grunstein, Schedl and Kedes, 1973a; Grunstein and Schedl, 1976). Spacer regions of unknown function account for nearly 60% of the repeat unit and separate the five coding regions (Kedes and Birnstiel, 1971; Portmann et al., 1976; Wu et al., 1976; Holmes et al., 1977). There are striking parallels in structure between hDNA and other repeated genes such as the 28+ 18s ribosomal genes and the 5s ribosomal genes of Xenopus laevis. One major difference, however, is the apparent lack of length or sequence heterogeneity of the hDNA (Kedes, 1976). The length of the repeating unit appears