Terracol R, Prud'homme N
Mol Cell Biol. 1986 Apr;6(4):1023-31. doi: 10.1128/mcb.6.4.1023-1031.1986.
In Drosophila melanogaster, the multiply repeated genes encoding 18S and 28S rRNA are located on the X and Y chromosomes. A large percentage of these repeats are interrupted in the 28S region by insertions of two types. We compared the restriction patterns from a subcloned wild-type Oregon R strain to those of spontaneous and ethyl methanesulfonate-induced bobbed mutants. Bobbed mutations were found to be deficiencies that modified the organization of the rDNA locus. Genes without insertions were deleted about twice as often as genes with type I insertions. Type II insertion genes were not decreased in number, except in the mutant having the most bobbed phenotype. Reversion to wild type was associated with an increase in gene copy number, affecting exclusively genes without insertions. One hypothesis which explains these results is the partial clustering of genes by type. The initial deletion could then be due either to an unequal crossover or to loss of material without exchange. Some of our findings indicated that deletion may be associated with an amplification phenomenon, the magnitude of which would be dependent on the amount of clustering of specific gene types at the locus.
在黑腹果蝇中,编码18S和28S rRNA的多重重复基因位于X和Y染色体上。这些重复序列中有很大一部分在28S区域被两种类型的插入序列打断。我们将亚克隆的野生型俄勒冈R品系的限制性酶切图谱与自发和甲磺酸乙酯诱导的截毛突变体的图谱进行了比较。发现截毛突变是改变rDNA位点组织的缺失。没有插入序列的基因被删除的频率大约是有I型插入序列基因的两倍。II型插入基因的数量没有减少,除了具有最截毛表型的突变体。回复到野生型与基因拷贝数的增加有关,仅影响没有插入序列的基因。一个解释这些结果的假说是基因按类型部分聚类。最初的缺失可能是由于不等交换或无交换的物质丢失。我们的一些发现表明,缺失可能与一种扩增现象有关,其程度将取决于该位点特定基因类型的聚类量。