Rasmuson A
Mutat Res. 1985 Jan-Feb;148(1-2):65-70. doi: 10.1016/0027-5107(85)90208-8.
An unstable white locus in Drosophila melanogaster originally described by Rasmuson and Green (1974) and further by Rasmuson et al. (1978, 1980) contains an IS element. This constellation interacts with the zeste mutation and forms a mutationally unstable system that is sensitive to a variety of mutagens. Mutational shifts between zeste and wild-type eye color as well as deletions and transpositions of the white locus are frequently occurring in the unstable X-chromosome in germ line and in somatic tissue. Germinal mutations from zeste to wild-type eye color are associated with an insertion of a piece of DNA, proximal to the wsp site, and the shifts from red to zeste are caused by an excision of the same piece (Rasmuson, in preparation). Mutations to pigmentless phenotype are interpreted as deletions of the white locus, while they always are irreversible and show non-complementation with wsp. The somatic system can be used as a screening test for potential mutagens, described by Rasmuson et al. (1984). This survey is an attempt to correlate the size of the mutated area of the eyes with the age of the larvae at mutagen treatment. X-Rays and MMS were used to give an indication of the mechanism of the instability, according to the different kinds of DNA damage induced. The results show that the mean size of red spots decreased with increasing age of larvae at treatment, while the mutation frequencies were increased because of the multiplication of the cells in the eye anlage susceptible to the mutagens. This is contradictory to the hypothesis maintained by Fahmy and Fahmy (1980) that the somatic shifts are not mutagenic but epigenetic events, due to altered regulation of the gene expression. Red spots induced with MMS are smaller in size than X-ray-induced red spots, indicating a delay in the establishment of mutations from chemically-induced lesions compared to irradiation damage. White spots on the other hand were equally large in size, irrespective of inducing agent and about twice the size of the chemically-induced red spots, implying a faster and more direct action for fixation of deletions than for the production of MMS induced shifts in eye color from zeste to red.
果蝇中一个不稳定的白色位点最初由拉斯穆森和格林(1974年)描述,拉斯穆森等人(1978年、1980年)进一步研究发现该位点含有一个插入序列(IS元件)。这种组合与小体突变相互作用,形成一个对多种诱变剂敏感的突变不稳定系统。在生殖系和体细胞组织的不稳定X染色体中,经常发生小体与野生型眼色之间的突变转换以及白色位点的缺失和转位。从黄色到野生型眼色的生殖突变与一段DNA的插入有关,该插入位于wsp位点近端,而从红色到黄色的转换是由同一段DNA的切除引起的(拉斯穆森,正在准备中)。无色素表型的突变被解释为白色位点的缺失,这些突变总是不可逆的,并且与wsp表现出非互补性。体细胞系统可作为潜在诱变剂的筛选试验,这由拉斯穆森等人(1984年)描述。本研究试图将诱变处理时幼虫的年龄与眼睛突变区域的大小联系起来。根据诱导的不同类型的DNA损伤,使用X射线和甲基磺酸甲酯(MMS)来揭示不稳定性的机制。结果表明,处理时幼虫年龄越大,红色斑点的平均大小越小,而由于眼原基中易受诱变剂影响的细胞增殖,突变频率增加。这与法赫米和法赫米(1980年)提出的假设相矛盾,他们认为体细胞转换不是诱变事件,而是由于基因表达调控改变导致的表观遗传事件。MMS诱导的红色斑点比X射线诱导的红色斑点尺寸更小,这表明与辐射损伤相比,化学诱导损伤导致的突变建立存在延迟。另一方面,白色斑点的大小相同,与诱导剂无关,大约是化学诱导红色斑点大小的两倍,这意味着缺失的固定作用比MMS诱导的眼色从黄色到红色的转换作用更快、更直接。