Pederson D S, Yao M C, Kimmel A R, Gorovsky M A
Nucleic Acids Res. 1984 Mar 26;12(6):3003-21. doi: 10.1093/nar/12.6.3003.
Macro- and micronuclei of Tetrahymena thermophila each contain approximately 30 clusters of 5S genes per haploid genome. Structural changes in DNA sequences associated with some of these clusters occur during the development of the transcriptionally active macronucleus from the transcriptionally inert micronucleus. Exonuclease digestion indicates that DNA fragmentation is not responsible for these changes, making it likely that sequence rearrangements occur near some 5S genes during macronuclear development. These rearrangements appear to be random in location with respect to the 5S genes and do not alter either the tandem repeat organization of the genes, the average number (five) or the range in number (one to about 16) of genes per cluster. The 5S gene clusters are not closely linked and are not flanked by common repeating elements large enough to cross-hybridize. Sequence analysis of one tandem repeat suggests that Tetrahymena 5S genes have intragenic promoters. These observations indicate that features other than DNA rearrangements or DNA sequence per se are responsible for the transcriptional activation of 5S genes during macronuclear development.
嗜热四膜虫的大核和微核每个单倍体基因组中大约包含30个5S基因簇。在转录惰性的微核发育为转录活性大核的过程中,与其中一些基因簇相关的DNA序列会发生结构变化。核酸外切酶消化表明,DNA片段化并非这些变化的原因,这使得在大核发育过程中,5S基因附近可能发生了序列重排。这些重排在相对于5S基因的位置上似乎是随机的,并且既不改变基因的串联重复组织,也不改变每个基因簇中基因的平均数量(五个)或数量范围(一到约16个)。5S基因簇并非紧密相连,也没有被大到足以交叉杂交的常见重复元件侧翼包围。对一个串联重复序列的序列分析表明,嗜热四膜虫的5S基因具有基因内启动子。这些观察结果表明,在大核发育过程中,除了DNA重排或DNA序列本身之外,其他特征才是5S基因转录激活的原因。