Chang W X, Gahan L J, Tabashnik B E, Heckel D G
Department of Entomology, University of Hawaii, Honolulu 96822, USA.
Insect Mol Biol. 1999 May;8(2):171-7. doi: 10.1046/j.1365-2583.1999.820171.x.
We screened a midgut cDNA library from diamondback moth, Plutella xylostella, with a probe generated using sequence information from an aminopeptidase N gene from Manduca sexta (MsAPN-1). The sequence recovered (PxAPN-A) encodes a protein of 988 resides with a 60% sequence identity to MsAPN-1. The two proteins share a signal peptide which directs processing by the endoplasmic reticulum, a C-terminal hydrophobic region satisfying the criterion for a GPI anchor and cleavage, and the possibility of an O-glycosylated rigid stalk attached to the GPI anchor. PxAPN-A is more closely related to MsAPN-1 than it is to another aminopeptidase recently reported from P. xylostella. Sequence comparisons with other species suggests that at least one aminopeptidase gene duplication occurred in an ancestral lepidopteran.
我们用源于烟草天蛾(Manduca sexta)的氨肽酶N基因(MsAPN-1)的序列信息制备的探针,筛选了小菜蛾(Plutella xylostella)的中肠cDNA文库。获得的序列(PxAPN-A)编码一个含988个氨基酸残基的蛋白质,与MsAPN-1有60%的序列同一性。这两种蛋白质共有一个由内质网进行加工处理的信号肽、一个满足GPI锚定和切割标准的C端疏水区域,以及一个连接到GPI锚定上的O-糖基化刚性茎的可能性。与小菜蛾最近报道的另一种氨肽酶相比,PxAPN-A与MsAPN-1的关系更为密切。与其他物种的序列比较表明,在鳞翅目祖先中至少发生了一次氨肽酶基因复制。