Barany F, Kahn M E, Smith H O
Proc Natl Acad Sci U S A. 1983 Dec;80(23):7274-8. doi: 10.1073/pnas.80.23.7274.
DNA transport and integration in Haemophilus influenzae transformation was studied with a plasmid clone of homologous DNA (pCML6). Our results indicate that: (i) donor DNA enters specialized membranous extensions on the cell surface, which we have termed "transformasomes"; (ii) linear DNA undergoes degradation upon exiting transformasomes; and (iii) DNA without a free end remains within transformasomes and is not degraded. By comparing the fate of label from uniformly labeled versus middle-labeled DNA, it appears that donor DNA undergoes degradation from an end prior to recombining with the chromosome. Using donor DNA with covalently closed termini (hairpin ends) prevents efficient exit from transformasomes. When one hairpin is removed, exit of donor DNA is shown to be directional from the free end, with preferential homologous integration of the 3' strand from that end.
利用同源DNA的质粒克隆(pCML6)研究了流感嗜血杆菌转化过程中的DNA转运与整合。我们的结果表明:(i)供体DNA进入细胞表面特化的膜性延伸结构,我们将其称为“转化体”;(ii)线性DNA在离开转化体时会发生降解;(iii)没有自由末端的DNA保留在转化体中且不会被降解。通过比较均匀标记与中间标记DNA的标记命运,似乎供体DNA在与染色体重组之前从一端开始降解。使用具有共价封闭末端(发夹末端)的供体DNA会阻止其从转化体中有效退出。当去除一个发夹时,供体DNA从自由末端的退出显示为具有方向性,该末端的3'链优先进行同源整合。