摘要
从实验室饲养的3种家鼠寄生蚤,印鼠客蚤(Xenopsyllacheopis)、缓慢细蚤(Leptopsyllasegnis)和不等单蚤(Monopsyllusanisus)制备出基因组DNA,用8种识别不同位点的限制性内切酶EcoRI,HindⅢ,PastI,SalI,BamHI,HpaI,PvuⅡ,BglI对蚤基因组DNA进行单酶完全酶切分析。印鼠客蚤基因组DNA经EcoRI酶解电泳后,见6条带,分别为3.22kb,2.93kb,2.20kb,1.57kb,1.53kb,1.48kb,缓慢细蚤与不等单蚤仅见一条,分别为5.79kb和7.01kb。经BamHI酶切,印鼠客蚤DNA见1条2.54kb的带,缓慢细蚤与不等单蚤分别有2条,各为7.35kb,0.59kb和12.29kb,0。62kb。另外,印鼠客蚤经HpaI酶切后,还有2条分子量很相近的DNA带型,分别为1.56kb,1.54kb。此外,3种蚤在其他内切酶酶切产物中未显肉眼可见的电泳带型。酶切结果显示缓慢细蚤与不等单蚤很相似,这2种蚤具有较大的同源性,说明其亲缘关系较近。印鼠客蚤酶切产物与另外2种蚤差别很大,提示它在蚤的进化过种中较早分化出来,故与?
Genomic DNA from three species of domestic rat flea,Leptosylla segnis,Mon0psyllus anisus and xenopsylla cheopis,were prepared,then digested with eight restriction enzymes. In digestion with EcoR I and electrophoresis,the genomic DNA of X.cheopis showed six bands(3. 22 kb,2. 93 kb,2.20 kb,1.57 kb,1.53 kb,1.48 kb),while only one band in L.segnis(5. 79 kb)and in M.anisus(7. 01 kb).In the analysis of BamH I,the X.cheopis genomic DNA gave one band(2.54 kb),while L.segnis(7.35 kb,0.59 kb) and M.anisus (12.29 kb,0.62 kb)gave two bands,respectively.On the other hand,X. cheopis genomic DNA showed two bands( 1.56 kb,1.54 kb )in the HpaI experiment,but no bands in the other two species of fleas. The re-mained REs showed no visible bands in any of the three species’ DNA. The results of REs digestion in L. seg-nis and M. anisus were similar to each other,implicating that these two species were in close relatives;howev-e,the results of REs’digestion in X cheopis were much different from the other two species,suggesting it an earlier differentiation in phylogeny
出处
《地方病通报》
1995年第3期8-11,共4页
Endemic Diseases Bulletin
基金
福建省自然科学基金