Templeton A R, Crease T J, Shah F
Genetics. 1985 Dec;111(4):805-18. doi: 10.1093/genetics/111.4.805.
The abnormal abdomen syndrome (aa) in Drosophila mercatorum is characterized by the persistence of juvenilized cuticle on the adult abdomen. The aa phenotype is shown to depend on at least two X-linked genetic elements that are about one map unit apart near the centromeric end of the X chromosome. These two genetic elements are necessary for aa expression; one behaves as a dominant element and the other as a recessive. Overlaying these genetic studies upon molecular work reported elsewhere, it is argued that the dominant element is the presence of a 5 kb insertion in a majority of the X-linked repeats coding for the 28S ribosomal RNA. The recessive element appears to be a locus controlling differential replication of noninserted over inserted 28S genes during polytenization. The aa syndrome requires both the presence of the inserted repeats and the failure to preferentially amplify noninserted repeats. Given the necessary X-linked elements for aa, a variety of modifiers are revealed. First, aa expression in males is Y-linked, apparently corresponding to a deletion of the 18S/28S rDNA gene cluster normally found on the Y. Moreover, all major autosomes can modify the penetrance of aa.
墨氏果蝇的异常腹部综合征(aa)的特征是成虫腹部存在幼态化表皮。已表明aa表型取决于至少两个X连锁遗传元件,它们在X染色体着丝粒末端附近相距约一个图距。这两个遗传元件对aa表达是必需的;一个表现为显性元件,另一个表现为隐性元件。将这些遗传学研究与其他地方报道的分子研究相结合,有人认为显性元件是在大多数编码28S核糖体RNA的X连锁重复序列中存在一个5 kb的插入片段。隐性元件似乎是一个在多线化过程中控制未插入的28S基因相对于插入的28S基因进行差异复制的位点。aa综合征既需要插入重复序列的存在,也需要优先扩增未插入重复序列的失败。鉴于aa所需的X连锁元件,发现了多种修饰因子。首先,雄性中的aa表达是Y连锁的,显然对应于通常在Y染色体上发现的18S/28S rDNA基因簇的缺失。此外,所有主要常染色体都可以改变aa的外显率。