Pellegrini M, Manning J, Davidson N
Cell. 1977 Feb;10(2):213-4. doi: 10.1016/0092-8674(77)90215-x.
The sequence arrangement of genes coding for stable rRNA species and of the interspersed spacers on long single strands of rDNA purified from total chromosomal DNA of Drosophila melanogaster has been determined by a study of the structure of rRNA:DNA hybrids which were mounted for electron microscope observation by the gene 32-ethidium bromide technique. One repeat unit contains the following sequences in the order given. First, an 18 S gene of length 2.13 +/- 0.17 kb. Second, an internal transcribed spacer (Spl) of length 1.58 +/- 0.15 kb. A short sequence coding for the 5.8S and perhaps the 2S rRNA species is located within this spacer. Third, the 28S gene with a length of 4.36 +/- 0.23 kb. About 55% of the 28S genes are unbroken or continuous (C genes). However, about 45% of the 28S genes contain an insertion of an additional segment of DNA that is not complementary to rRNA (l genes). The insertion occurs at a reproducible point 2.99 +/- 0.26 kb from the junction with Spl. The insertions are heterogeneous in length and occur in three broad size classes: 1.42 +/- 0.47, 3.97 +/- 0.55, and 6.59 +/- 0.62 kb. Fourth, an external spacer between the 28S gene and the next 18S gene which is presumably mainly nontranscribed and which has a heterogeneous length distribution with a mean length and standard deviation of 5.67 +/- 1.92 kb. Short inverted repeat stems (100-400 nucleotide pairs) occur at the base of the insertion. It is known from other studies that I genes occur only on the X chromosome. The present study shows that the I and C genes on the X chromosomes are approximately randomly assorted. The sequence arrangement on the plasmid pDm103 containing one repeat of rDNA (Glover et al., 1975) has been determined by similar methods. The I gene on this plasmid contains an inverted repeat stem. The occurrence of inverted repeat sequences flanking the insertion supports the speculation that these sequences are translocatable elements similar to procaryotic translocons.
通过对用基因32 - 溴化乙锭技术制备用于电子显微镜观察的rRNA:DNA杂交体结构的研究,已确定了从黑腹果蝇总染色体DNA中纯化的rDNA长单链上编码稳定rRNA种类的基因及散布间隔区的序列排列。一个重复单元按给定顺序包含以下序列。首先,长度为2.13±0.17 kb的18S基因。其次,长度为1.58±0.15 kb的内部转录间隔区(Spl)。编码5.8S及可能的2S rRNA种类的短序列位于该间隔区内。第三,长度为4.36±0.23 kb的28S基因。约55%的28S基因是完整的或连续的(C基因)。然而,约45%的28S基因含有一段与rRNA不互补的额外DNA片段插入(I基因)。插入发生在距与Spl交界处2.99±0.26 kb的可重复位点。插入片段长度各异,分为三个大致的大小类别:1.42±0.47、3.97±0.55和6.59±0.62 kb。第四,28S基因与下一个18S基因之间的外部间隔区,推测主要是非转录的,其长度分布不均一,平均长度和标准差为5.67±1.92 kb。短的反向重复茎(100 - 400个核苷酸对)出现在插入片段的基部。从其他研究已知I基因仅存在于X染色体上。本研究表明X染色体上的I基因和C基因大致随机排列。通过类似方法已确定了含有一个rDNA重复序列的质粒pDm103上的序列排列(格洛弗等人,1975年)。该质粒上的I基因含有一个反向重复茎。插入片段两侧出现反向重复序列支持了这样的推测,即这些序列是类似于原核转座子的可转位元件。