Reed D S, Gibson J B
Research School of Biological Sciences, Australian National University, Canberra City, A.C.T.
Proc Biol Sci. 1993 Jan 22;251(1330):39-45. doi: 10.1098/rspb.1993.0006.
A distinctive and geographically widespread category of low-activity variant at the Gpdh locus in Drosophila melanogaster is shown to have defective P elements inserted between the TATA box and the transcription start site. In four examples the insertion was a single 1.15 kilobase (kb) KP element, whereas in another variant there were two KP elements in tandem. A sixth example contained a 0.61 kb defective P element. The target site for all of the insertions is GTGCAAAC. There was no sequence variation either between the insertions or in comparison with two other KP elements previously described from natural populations. The insertions cause a reduction in GPDH mRNA, and are the most likely cause of the low GPDH activity.
在黑腹果蝇的Gpdh基因座上,一类独特且在地理上广泛分布的低活性变体被证明在TATA框和转录起始位点之间插入了有缺陷的P因子。在四个例子中,插入的是单个1.15千碱基(kb)的KP因子,而在另一个变体中则有两个串联的KP因子。第六个例子包含一个0.61 kb的有缺陷的P因子。所有插入的靶位点都是GTGCAAAC。插入之间以及与先前从自然种群中描述的另外两个KP因子相比,均不存在序列变异。这些插入导致GPDH mRNA减少,并且最有可能是GPDH活性低的原因。